association	dataset	threshold value	standardized value
sporadic	GeneRIF Biological Term Annotations	1.0	null
multiple lipomas	HPO Gene-Disease Associations	1.0	null
PL-21	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	1.07705
diabetes mellitus type ii; diabetes mellitus, type 2	GAD Gene-Disease Associations	1.0	null
Gait Disorders, Neurologic	HuGE Navigator Gene-Phenotype Associations	1.0	null
gingival overgrowth	HPO Gene-Disease Associations	1.0	null
abnormality of the urinary system physiology	HPO Gene-Disease Associations	1.0	null
pulmonary hypertension	HPO Gene-Disease Associations	1.0	null
memory impairment	HPO Gene-Disease Associations	1.0	null
BT-549	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-1.0667
C32TG	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-0.921797
G122	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-1.30792
retinal	GeneRIF Biological Term Annotations	1.0	null
abnormal renal morphology	HPO Gene-Disease Associations	1.0	null
abnormality of the intestine	HPO Gene-Disease Associations	1.0	null
abnormality of central nervous system electrophysiology	HPO Gene-Disease Associations	1.0	null
HCC2302	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-0.909071
abnormality of movement	HPO Gene-Disease Associations	1.0	null
mellitus	GeneRIF Biological Term Annotations	1.0	null
contributing	GeneRIF Biological Term Annotations	1.0	null
Alzheimer Disease	HuGE Navigator Gene-Phenotype Associations	1.0	null
flexion contracture	HPO Gene-Disease Associations	1.0	null
A2780	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	0.886236
abnormality of cerebral artery	HPO Gene-Disease Associations	1.0	null
overexpression	GeneRIF Biological Term Annotations	1.0	null
HCC4017	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	1.10402
biogenesis	GeneRIF Biological Term Annotations	1.0	null
abnormality of forebrain morphology	HPO Gene-Disease Associations	1.0	null
localized skin lesion	HPO Gene-Disease Associations	1.0	null
hypertrophic	GeneRIF Biological Term Annotations	1.0	null
cerebral atrophy	HPO Gene-Disease Associations	1.0	null
NCI-H1666	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	1.07705
PE/CA-PJ15	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-0.922079
respiratory	GeneRIF Biological Term Annotations	1.0	null
abnormality of the optic disc	HPO Gene-Disease Associations	1.0	null
abnormality of the middle ear	HPO Gene-Disease Associations	1.0	null
abnormality of the skull	HPO Gene-Disease Associations	1.0	null
regeneration	GeneRIF Biological Term Annotations	1.0	null
characteristics	GeneRIF Biological Term Annotations	1.0	null
abnormality of the abdominal organs	HPO Gene-Disease Associations	1.0	null
detrimental	GeneRIF Biological Term Annotations	1.0	null
diabetes	GeneRIF Biological Term Annotations	1.0	null
Autoimmune Diseases	HuGE Navigator Gene-Phenotype Associations	1.0	null
abnormality of the orbital region	HPO Gene-Disease Associations	1.0	null
incidence	GeneRIF Biological Term Annotations	1.0	null
G84	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-1.25508
reduction	GeneRIF Biological Term Annotations	1.0	null
KMS-28BM	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	1.95465
IMR-32	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	0.83674
Insulin Resistance	HuGE Navigator Gene-Phenotype Associations	1.0	null
abnormal eye morphology	HPO Gene-Disease Associations	1.0	null
abnormality of skeletal morphology	HPO Gene-Disease Associations	1.0	null
abnormality of the nervous system	HPO Gene-Disease Associations	1.0	null
Hearing Disorders	HuGE Navigator Gene-Phenotype Associations	1.0	null
deafness; diabetes mellitus, type 1; diabetes mellitus, type 2; mitochondrial diseases	GAD Gene-Disease Associations	1.0	null
NCI-H1944	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	1.21083
OKAJIMA	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-1.56778
abnormality of eye movement	HPO Gene-Disease Associations	1.0	null
neurodevelopmental abnormality	HPO Gene-Disease Associations	1.0	null
SW 948	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	1.73939
melas syndrome; merrf syndrome	GAD Gene-Disease Associations	1.0	null
vascular skin abnormality	HPO Gene-Disease Associations	1.0	null
EB2	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	1.06424
growth abnormality	HPO Gene-Disease Associations	1.0	null
CL-34	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	1.33292
neoplasm by anatomical site	HPO Gene-Disease Associations	1.0	null
abnormality of connective tissue	HPO Gene-Disease Associations	1.0	null
generalized abnormality of skin	HPO Gene-Disease Associations	1.0	null
pathogenesis	GeneRIF Biological Term Annotations	1.0	null
abnormality of the cerebral vasculature	HPO Gene-Disease Associations	1.0	null
diabetes mellitus; hearing disorders; hearing problem; mitochondrial diseases	GAD Gene-Disease Associations	1.0	null
glomerulopathy	HPO Gene-Disease Associations	1.0	null
incoordination	HPO Gene-Disease Associations	1.0	null
abnormality of calcium homeostasis	HPO Gene-Disease Associations	1.0	null
abnormality of urine calcium concentration	HPO Gene-Disease Associations	1.0	null
muscle	GeneRIF Biological Term Annotations	1.0	null
genetic diseases, inborn; hearing impairment; hearing loss	GAD Gene-Disease Associations	1.0	null
individuals	GeneRIF Biological Term Annotations	1.0	null
hemiplegia/hemiparesis	HPO Gene-Disease Associations	1.0	null
OCI-AML3	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	1.70423
GP5D	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	1.63963
pulmonary embolism	HPO Gene-Disease Associations	1.0	null
FU97	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-0.827235
SK-N-FI	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-1.88207
cardiac	GeneRIF Biological Term Annotations	1.0	null
L-363	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	1.221
abnormality of joint mobility	HPO Gene-Disease Associations	1.0	null
AMO-1	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	1.36087
Atrophy	HuGE Navigator Gene-Phenotype Associations	1.0	null
reduced tendon reflexes	HPO Gene-Disease Associations	1.0	null
Diabetic Retinopathy	HuGE Navigator Gene-Phenotype Associations	1.0	null
hypertension	HPO Gene-Disease Associations	1.0	null
OPM-2	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	1.19399
Cardiovascular Diseases	HuGE Navigator Gene-Phenotype Associations	1.0	null
myopathy	GeneRIF Biological Term Annotations	1.0	null
abnormality of the myocardium	HPO Gene-Disease Associations	1.0	null
spontaneous hematomas	HPO Gene-Disease Associations	1.0	null
abnormality of the fundus	HPO Gene-Disease Associations	1.0	null
aplasia/hypoplasia of the cerebellum	HPO Gene-Disease Associations	1.0	null
abnormality of the renal tubule	HPO Gene-Disease Associations	1.0	null
suppressed	GeneRIF Biological Term Annotations	1.0	null
cause	GeneRIF Biological Term Annotations	1.0	null
Diabetes Mellitus	HuGE Navigator Gene-Phenotype Associations	1.0	null
abnormality of the respiratory system	HPO Gene-Disease Associations	1.0	null
Obesity	HuGE Navigator Gene-Phenotype Associations	1.0	null
PK-45H	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	1.33691
a3243g	GeneRIF Biological Term Annotations	1.0	null
sclerosis	GeneRIF Biological Term Annotations	1.0	null
migraine	HPO Gene-Disease Associations	1.0	null
NCI-H889	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	1.22811
Chronic Disease	HuGE Navigator Gene-Phenotype Associations	1.0	null
ophthalmoparesis	HPO Gene-Disease Associations	1.0	null
Hyperglycemia	HuGE Navigator Gene-Phenotype Associations	1.0	null
MKN-1	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-1.03747
abnormality of vision evoked potentials	HPO Gene-Disease Associations	1.0	null
abnormality of the globe	HPO Gene-Disease Associations	1.0	null
hearing abnormality	HPO Gene-Disease Associations	1.0	null
headache	HPO Gene-Disease Associations	1.0	null
LS 180	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-1.43928
turnover	GeneRIF Biological Term Annotations	1.0	null
abnormality of the mitochondrion	HPO Gene-Disease Associations	1.0	null
defined	GeneRIF Biological Term Annotations	1.0	null
atrophy/degeneration affecting the central nervous system	HPO Gene-Disease Associations	1.0	null
hearing loss, sensorineural; learning disorders; melas syndrome; migraine disorders; mitochondrial diseases; sensorineural hearing loss	GAD Gene-Disease Associations	1.0	null
dystrophy	GeneRIF Biological Term Annotations	1.0	null
abnormality of neuronal migration	HPO Gene-Disease Associations	1.0	null
MDA-MB-175-VII	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-0.836384
positively	GeneRIF Biological Term Annotations	1.0	null
malabsorption	HPO Gene-Disease Associations	1.0	null
MS751	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-1.02302
affects	GeneRIF Biological Term Annotations	1.0	null
abnormality of the gingiva	HPO Gene-Disease Associations	1.0	null
thyroiditis	HPO Gene-Disease Associations	1.0	null
night blindness	HPO Gene-Disease Associations	1.0	null
abnormality of peripheral nerve conduction	HPO Gene-Disease Associations	1.0	null
muscle weakness	HPO Gene-Disease Associations	1.0	null
sensorineural hearing impairment	HPO Gene-Disease Associations	1.0	null
decreased body weight	HPO Gene-Disease Associations	1.0	null
optic atrophy	HPO Gene-Disease Associations	1.0	null
peripheral neuropathy	HPO Gene-Disease Associations	1.0	null
abnormality of adrenal physiology	HPO Gene-Disease Associations	1.0	null
cardiomyopathy	GeneRIF Biological Term Annotations	1.0	null
Migraine Disorders	HuGE Navigator Gene-Phenotype Associations	1.0	null
lipomatous tumor	HPO Gene-Disease Associations	1.0	null
Pancreatitis	HuGE Navigator Gene-Phenotype Associations	1.0	null
trnaleu	GeneRIF Biological Term Annotations	1.0	null
abnormality of the integument	HPO Gene-Disease Associations	1.0	null
microcephaly	HPO Gene-Disease Associations	1.0	null
HM7	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-2.59311
TOV-112D	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	0.946961
abnormality of the inner ear	HPO Gene-Disease Associations	1.0	null
abnormal renal physiology	HPO Gene-Disease Associations	1.0	null
epidermal thickening	HPO Gene-Disease Associations	1.0	null
LN-18	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-1.40099
trnaleuuur	GeneRIF Biological Term Annotations	1.0	null
isolated	GeneRIF Biological Term Annotations	1.0	null
multiple	GeneRIF Biological Term Annotations	1.0	null
alzheimer disease; ataxia; diabetes mellitus, type 2; disease; obesity; parkinson disease	GAD Gene-Disease Associations	1.0	null
mask-like facies	HPO Gene-Disease Associations	1.0	null
growth delay	HPO Gene-Disease Associations	1.0	null
coding	GeneRIF Biological Term Annotations	1.0	null
KM-12	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-0.839913
abnormality of oral mucosa	HPO Gene-Disease Associations	1.0	null
abnormality of lipid metabolism	HPO Gene-Disease Associations	1.0	null
phenotypic	GeneRIF Biological Term Annotations	1.0	null
mtdna	GeneRIF Biological Term Annotations	1.0	null
functional abnormality of the inner ear	HPO Gene-Disease Associations	1.0	null
NCI-H2595	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-1.06964
KCI-MOH1	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	0.851099
abdominal pain	HPO Gene-Disease Associations	1.0	null
deficiency	GeneRIF Biological Term Annotations	1.0	null
abnormal peripheral nervous system morphology	HPO Gene-Disease Associations	1.0	null
decrease	GeneRIF Biological Term Annotations	1.0	null
defect	GeneRIF Biological Term Annotations	1.0	null
merrfmelas	GeneRIF Biological Term Annotations	1.0	null
abnormal hair quantity	HPO Gene-Disease Associations	1.0	null
ectopic calcification	HPO Gene-Disease Associations	1.0	null
abnormality of cation homeostasis	HPO Gene-Disease Associations	1.0	null
abnormality of the musculature	HPO Gene-Disease Associations	1.0	null
MCF 10A	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-0.929347
501A	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	1.25516
ici	GeneRIF Biological Term Annotations	1.0	null
abnormality of the pulmonary artery	HPO Gene-Disease Associations	1.0	null
SNU-668	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	1.08257
abnormal urinary electrolyte concentration	HPO Gene-Disease Associations	1.0	null
mutant	GeneRIF Biological Term Annotations	1.0	null
SR-786	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-0.938784
Acidosis, Lactic	CTD Gene-Disease Associations	1.0	2.88009
mitochondrial	GeneRIF Biological Term Annotations	1.0	null
abnormality of skin adnexa	HPO Gene-Disease Associations	1.0	null
caused	GeneRIF Biological Term Annotations	1.0	null
goiter	HPO Gene-Disease Associations	1.0	null
visual field defect	HPO Gene-Disease Associations	1.0	null
cerebral cortical atrophy	HPO Gene-Disease Associations	1.0	null
abnormality of the macula	HPO Gene-Disease Associations	1.0	null
abnormal pyramidal signs	HPO Gene-Disease Associations	1.0	null
Carotid Artery Diseases	HuGE Navigator Gene-Phenotype Associations	1.0	null
Diabetic Neuropathies	HuGE Navigator Gene-Phenotype Associations	1.0	null
A-375	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-2.19993
abnormality of urine homeostasis	HPO Gene-Disease Associations	1.0	null
cataract	HPO Gene-Disease Associations	1.0	null
neoplasm of fatty tissue	HPO Gene-Disease Associations	1.0	null
symptoms	GeneRIF Biological Term Annotations	1.0	null
inherited	GeneRIF Biological Term Annotations	1.0	null
abnormality of the adrenal glands	HPO Gene-Disease Associations	1.0	null
JJ012	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-1.49356
level	GeneRIF Biological Term Annotations	1.0	null
Leigh Disease	HuGE Navigator Gene-Phenotype Associations	1.0	null
abnormality of the lung	HPO Gene-Disease Associations	1.0	null
abnormality of central motor function	HPO Gene-Disease Associations	1.0	null
Hearing Loss	HuGE Navigator Gene-Phenotype Associations	1.0	null
diabetes, type 2	GAD Gene-Disease Associations	1.0	null
atrophy/degeneration affecting the cerebrum	HPO Gene-Disease Associations	1.0	null
HCC12	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-1.49314
carious teeth	HPO Gene-Disease Associations	1.0	null
Genetic Diseases, Inborn	HuGE Navigator Gene-Phenotype Associations	1.0	null
abnormal glucose homeostasis	HPO Gene-Disease Associations	1.0	null
metabolism	GeneRIF Biological Term Annotations	1.0	null
pathogenic	GeneRIF Biological Term Annotations	1.0	null
specific	GeneRIF Biological Term Annotations	1.0	null
reported	GeneRIF Biological Term Annotations	1.0	null
skeletal muscle atrophy	HPO Gene-Disease Associations	1.0	null
concludes	GeneRIF Biological Term Annotations	1.0	null
compensated	GeneRIF Biological Term Annotations	1.0	null
lactic	GeneRIF Biological Term Annotations	1.0	null
abnormality of the parathyroid physiology	HPO Gene-Disease Associations	1.0	null
Mitochondrial Diseases	HuGE Navigator Gene-Phenotype Associations	1.0	null
MDA-MB-453	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-0.91283
Wolff-Parkinson-White Syndrome	HuGE Navigator Gene-Phenotype Associations	1.0	null
Mitochondrial Encephalomyopathies	CTD Gene-Disease Associations	1.0	2.88009
abnormality of nervous system morphology	HPO Gene-Disease Associations	1.0	null
abnormality of the anterior pituitary	HPO Gene-Disease Associations	1.0	null
paresthesia	HPO Gene-Disease Associations	1.0	null
abnormality of the cerebrum	HPO Gene-Disease Associations	1.0	null
syndrome	GeneRIF Biological Term Annotations	1.0	null
Muscular Dystrophies	HuGE Navigator Gene-Phenotype Associations	1.0	null
hypothyroidism	HPO Gene-Disease Associations	1.0	null
encephalopathy	GeneRIF Biological Term Annotations	1.0	null
abnormality of the cerebellum	HPO Gene-Disease Associations	1.0	null
MV-4-11	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	0.938783
capacity	GeneRIF Biological Term Annotations	1.0	null
abnormality of the glomerulus	HPO Gene-Disease Associations	1.0	null
HT-1080	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-1.12447
abnormality of divalent inorganic cation homeostasis	HPO Gene-Disease Associations	1.0	null
Disease	HuGE Navigator Gene-Phenotype Associations	1.0	null
abnormality of the head	HPO Gene-Disease Associations	1.0	null
abnormality of the retinal pigment epithelium	HPO Gene-Disease Associations	1.0	null
steadystate	GeneRIF Biological Term Annotations	1.0	null
abnormality of the liver	HPO Gene-Disease Associations	1.0	null
adrenal insufficiency	HPO Gene-Disease Associations	1.0	null
Demyelinating Diseases	HuGE Navigator Gene-Phenotype Associations	1.0	null
upper motor neuron dysfunction	HPO Gene-Disease Associations	1.0	null
abnormality of the vasculature	HPO Gene-Disease Associations	1.0	null
CAL 27	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-0.942839
mitochondrial diseases	GAD Gene-Disease Associations	1.0	null
death	GeneRIF Biological Term Annotations	1.0	null
efg2	GeneRIF Biological Term Annotations	1.0	null
trnalys	GeneRIF Biological Term Annotations	1.0	null
BEN	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-1.05822
hypertrophic cardiomyopathy	HPO Gene-Disease Associations	1.0	null
abnormality of the uvea	HPO Gene-Disease Associations	1.0	null
abnormality of cardiac morphology	HPO Gene-Disease Associations	1.0	null
chorioretinal abnormality	HPO Gene-Disease Associations	1.0	null
inner	GeneRIF Biological Term Annotations	1.0	null
events	GeneRIF Biological Term Annotations	1.0	null
deafness	GeneRIF Biological Term Annotations	1.0	null
abnormality of body height	HPO Gene-Disease Associations	1.0	null
Retinal Dystrophies	HuGE Navigator Gene-Phenotype Associations	1.0	null
causes	GeneRIF Biological Term Annotations	1.0	null
abnormal pattern of respiration	HPO Gene-Disease Associations	1.0	null
LP-1	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	1.166
abnormality of the mouth	HPO Gene-Disease Associations	1.0	null
m3571inscmtnd1	GeneRIF Biological Term Annotations	1.0	null
Diabetic Nephropathies	HuGE Navigator Gene-Phenotype Associations	1.0	null
NCI-H1155	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-0.981658
ASXL1-24218140-BMDM-MOUSE	ChEA Transcription Factor Binding Site Profiles	1.0	null
abnormality of higher mental function	HPO Gene-Disease Associations	1.0	null
MM.1S	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	0.923134
Parkinson Disease	HuGE Navigator Gene-Phenotype Associations	1.0	null
germline	GeneRIF Biological Term Annotations	1.0	null
point	GeneRIF Biological Term Annotations	1.0	null
hypercalciuria	HPO Gene-Disease Associations	1.0	null
maternally	GeneRIF Biological Term Annotations	1.0	null
Plaque, Atherosclerotic	HuGE Navigator Gene-Phenotype Associations	1.0	null
morphological abnormality of the gastrointestinal tract	HPO Gene-Disease Associations	1.0	null
Diabetes Complications	HuGE Navigator Gene-Phenotype Associations	1.0	null
uug	GeneRIF Biological Term Annotations	1.0	null
heteroplasmy	GeneRIF Biological Term Annotations	1.0	null
severe	GeneRIF Biological Term Annotations	1.0	null
abnormality of the hair	HPO Gene-Disease Associations	1.0	null
autism	HPO Gene-Disease Associations	1.0	null
abnormal respiratory system morphology	HPO Gene-Disease Associations	1.0	null
Spinocerebellar Ataxias	HuGE Navigator Gene-Phenotype Associations	1.0	null
Stroke	HuGE Navigator Gene-Phenotype Associations	1.0	null
hypertelorism	HPO Gene-Disease Associations	1.0	null
Deafness	HuGE Navigator Gene-Phenotype Associations	1.0	null
decreased nerve conduction velocity	HPO Gene-Disease Associations	1.0	null
hearing loss	GAD Gene-Disease Associations	1.0	null
Lung Neoplasms	HuGE Navigator Gene-Phenotype Associations	1.0	null
SW 403	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	1.18131
ME-1	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	1.67142
abnormality of skull size	HPO Gene-Disease Associations	1.0	null
abnormal muscle tone	HPO Gene-Disease Associations	1.0	null
abnormality of the posterior segment of the eye	HPO Gene-Disease Associations	1.0	null
abnormality of the pinna	HPO Gene-Disease Associations	1.0	null
heteroplasmic	GeneRIF Biological Term Annotations	1.0	null
spinocerebellar ataxias	GAD Gene-Disease Associations	1.0	null
KG-1	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	0.827513
into	GeneRIF Biological Term Annotations	1.0	null
sensory neuropathy	HPO Gene-Disease Associations	1.0	null
SIG-M5	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	1.79286
abnormal tendon morphology	HPO Gene-Disease Associations	1.0	null
atherosclerosis	GeneRIF Biological Term Annotations	1.0	null
Intestinal Pseudo-Obstruction	HuGE Navigator Gene-Phenotype Associations	1.0	null
ASXL1	ChEA Transcription Factor Targets	1.0	null
abnormality of pancreas physiology	HPO Gene-Disease Associations	1.0	null
myopathy	HPO Gene-Disease Associations	1.0	null
hallucinations	HPO Gene-Disease Associations	1.0	null
ventriculomegaly	HPO Gene-Disease Associations	1.0	null
IGROV-1	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	0.886236
episodes	GeneRIF Biological Term Annotations	1.0	null
neoplasm	HPO Gene-Disease Associations	1.0	null
feeding difficulties in infancy	HPO Gene-Disease Associations	1.0	null
abnormality of cardiovascular system physiology	HPO Gene-Disease Associations	1.0	null
abnormality of the pituitary gland	HPO Gene-Disease Associations	1.0	null
sudden cardiac death	HPO Gene-Disease Associations	1.0	null
hearing impairment	HPO Gene-Disease Associations	1.0	null
abnormal nerve conduction velocity	HPO Gene-Disease Associations	1.0	null
short stature	HPO Gene-Disease Associations	1.0	null
muscular hypotonia	HPO Gene-Disease Associations	1.0	null
Ataxia	HuGE Navigator Gene-Phenotype Associations	1.0	null
ear	GeneRIF Biological Term Annotations	1.0	null
abnormality of nervous system physiology	HPO Gene-Disease Associations	1.0	null
Werner Syndrome	HuGE Navigator Gene-Phenotype Associations	1.0	null
abnormality of the eye	HPO Gene-Disease Associations	1.0	null
abnormal joint morphology	HPO Gene-Disease Associations	1.0	null
increasing	GeneRIF Biological Term Annotations	1.0	null
KASUMI-1	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	0.882805
abnormalities of the peripheral arteries	HPO Gene-Disease Associations	1.0	null
arthrogryposis multiplex congenita	HPO Gene-Disease Associations	1.0	null
respiratory insufficiency	HPO Gene-Disease Associations	1.0	null
BXPC-3	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-1.31696
hypopigmented skin patches	HPO Gene-Disease Associations	1.0	null
elevated pulmonary artery pressure	HPO Gene-Disease Associations	1.0	null
clinical	GeneRIF Biological Term Annotations	1.0	null
prevalent	GeneRIF Biological Term Annotations	1.0	null
constipation	HPO Gene-Disease Associations	1.0	null
NCI-H446	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-0.911631
involuntary movements	HPO Gene-Disease Associations	1.0	null
hyperactivity	HPO Gene-Disease Associations	1.0	null
functional abnormality of the gastrointestinal tract	HPO Gene-Disease Associations	1.0	null
cardiomyopathy	HPO Gene-Disease Associations	1.0	null
Cardiomyopathies	HuGE Navigator Gene-Phenotype Associations	1.0	null
strokelike	GeneRIF Biological Term Annotations	1.0	null
delayed skeletal maturation	HPO Gene-Disease Associations	1.0	null
Sick Sinus Syndrome	HuGE Navigator Gene-Phenotype Associations	1.0	null
being	GeneRIF Biological Term Annotations	1.0	null
abnormality of peripheral nervous system electrophysiology	HPO Gene-Disease Associations	1.0	null
apoptosis	GeneRIF Biological Term Annotations	1.0	null
alteration	GeneRIF Biological Term Annotations	1.0	null
overlap	GeneRIF Biological Term Annotations	1.0	null
COLO-818	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-1.12478
precursor	GeneRIF Biological Term Annotations	1.0	null
apnea	HPO Gene-Disease Associations	1.0	null
abdominal symptom	HPO Gene-Disease Associations	1.0	null
abnormality of peripheral nerves	HPO Gene-Disease Associations	1.0	null
Body Weight	HuGE Navigator Gene-Phenotype Associations	1.0	null
molecular	GeneRIF Biological Term Annotations	1.0	null
melas	GeneRIF Biological Term Annotations	1.0	null
Cytochrome-c Oxidase Deficiency	HuGE Navigator Gene-Phenotype Associations	1.0	null
congenital contracture	HPO Gene-Disease Associations	1.0	null
visual impairment	HPO Gene-Disease Associations	1.0	null
occurred	GeneRIF Biological Term Annotations	1.0	null
abnormality of the ear	HPO Gene-Disease Associations	1.0	null
abnormality of the upper urinary tract	HPO Gene-Disease Associations	1.0	null
m3460gamtnd1	GeneRIF Biological Term Annotations	1.0	null
upregulation	GeneRIF Biological Term Annotations	1.0	null
reduced consciousness/confusion	HPO Gene-Disease Associations	1.0	null
abnormality of the nephron	HPO Gene-Disease Associations	1.0	null
whereas	GeneRIF Biological Term Annotations	1.0	null
G96	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-1.12103
abnormality of dental structure	HPO Gene-Disease Associations	1.0	null
abnormal axial skeleton morphology	HPO Gene-Disease Associations	1.0	null
abnormality of the aorta	HPO Gene-Disease Associations	1.0	null
carrying	GeneRIF Biological Term Annotations	1.0	null
developmental regression	HPO Gene-Disease Associations	1.0	null
Aortic Diseases	HuGE Navigator Gene-Phenotype Associations	1.0	null
hypopigmentation of the skin	HPO Gene-Disease Associations	1.0	null
physiology	GeneRIF Biological Term Annotations	1.0	null
disorder	GeneRIF Biological Term Annotations	1.0	null
thickened skin	HPO Gene-Disease Associations	1.0	null
KMS-26	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	1.44654
abnormality of the thyroid gland	HPO Gene-Disease Associations	1.0	null
codonspecific	GeneRIF Biological Term Annotations	1.0	null
renal	GeneRIF Biological Term Annotations	1.0	null
NUGC-3	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-0.936648
abnormality of temperature regulation	HPO Gene-Disease Associations	1.0	null
produces	GeneRIF Biological Term Annotations	1.0	null
Glucose Intolerance	HuGE Navigator Gene-Phenotype Associations	1.0	null
biomarker	GeneRIF Biological Term Annotations	1.0	null
Kearns-Sayer Syndrome	HuGE Navigator Gene-Phenotype Associations	1.0	null
abnormality of the systemic arterial tree	HPO Gene-Disease Associations	1.0	null
severity	GeneRIF Biological Term Annotations	1.0	null
gastrointestinal obstruction	HPO Gene-Disease Associations	1.0	null
abnormality of the face	HPO Gene-Disease Associations	1.0	null
abnormality of coordination	HPO Gene-Disease Associations	1.0	null
abnormality of thyroid physiology	HPO Gene-Disease Associations	1.0	null
diabetes mellitus	HPO Gene-Disease Associations	1.0	null
anterior hypopituitarism	HPO Gene-Disease Associations	1.0	null
type ii diabetes mellitus	HPO Gene-Disease Associations	1.0	null
neurological speech impairment	HPO Gene-Disease Associations	1.0	null
HS 695T	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-1.01319
abnormality of skeletal maturation	HPO Gene-Disease Associations	1.0	null
NCI-H2081	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	0.830421
NCI-H1930	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-1.99089
SK-MM-2	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	1.06947
HCC4006	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-1.27722
represents	GeneRIF Biological Term Annotations	1.0	null
phosphorylation	GeneRIF Biological Term Annotations	1.0	null
proteinuria	HPO Gene-Disease Associations	1.0	null
Recurrence	HuGE Navigator Gene-Phenotype Associations	1.0	null
induced	GeneRIF Biological Term Annotations	1.0	null
myoblasts	GeneRIF Biological Term Annotations	1.0	null
JHH-1	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	0.900863
ptosis	HPO Gene-Disease Associations	1.0	null
abnormality of muscle morphology	HPO Gene-Disease Associations	1.0	null
Diabetic Ketoacidosis	HuGE Navigator Gene-Phenotype Associations	1.0	null
subcutaneous hemorrhage	HPO Gene-Disease Associations	1.0	null
translational	GeneRIF Biological Term Annotations	1.0	null
MELAS Syndrome	CTD Gene-Disease Associations	1.0	2.88009
Atherosclerosis	HuGE Navigator Gene-Phenotype Associations	1.0	null
105KC	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-2.19993
abnormality of the pancreas	HPO Gene-Disease Associations	1.0	null
abnormality of carbohydrate metabolism/homeostasis	HPO Gene-Disease Associations	1.0	null
abnormality of the cerebral ventricles	HPO Gene-Disease Associations	1.0	null
nausea and vomiting	HPO Gene-Disease Associations	1.0	null
abnormality of the pulmonary vasculature	HPO Gene-Disease Associations	1.0	null
transition	GeneRIF Biological Term Annotations	1.0	null
decreased facial expression	HPO Gene-Disease Associations	1.0	null
hypopituitarism	HPO Gene-Disease Associations	1.0	null
abnormal retinal pigmentation	HPO Gene-Disease Associations	1.0	null
trnaile	GeneRIF Biological Term Annotations	1.0	null
glucose	GeneRIF Biological Term Annotations	1.0	null
tremor	HPO Gene-Disease Associations	1.0	null
SNU-398	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	0.84149
retinopathy	HPO Gene-Disease Associations	1.0	null
MDA-MB-330	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	0.942986
indicated	GeneRIF Biological Term Annotations	1.0	null
Diabetes Mellitus, Type 2	HuGE Navigator Gene-Phenotype Associations	1.0	null
abnormality of the optic nerve	HPO Gene-Disease Associations	1.0	null
SW 982	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-0.999825
deafness; diabetes complications; diabetes mellitus; intestinal pseudo-obstruction; pancreatitis; recurrence	GAD Gene-Disease Associations	1.0	null
multisystemic	GeneRIF Biological Term Annotations	1.0	null
abnormality of the cardiovascular system	HPO Gene-Disease Associations	1.0	null
anorexia	HPO Gene-Disease Associations	1.0	null
Arrhythmia	HuGE Navigator Gene-Phenotype Associations	1.0	null
lifethreatening	GeneRIF Biological Term Annotations	1.0	null
Heart Diseases	HuGE Navigator Gene-Phenotype Associations	1.0	null
single	GeneRIF Biological Term Annotations	1.0	null
dysfunction	GeneRIF Biological Term Annotations	1.0	null
abnormal facial expression	HPO Gene-Disease Associations	1.0	null
LS 174T	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-1.66981
presentation	GeneRIF Biological Term Annotations	1.0	null
novo	GeneRIF Biological Term Annotations	1.0	null
HS 683	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-0.989471
earlier	GeneRIF Biological Term Annotations	1.0	null
wide	GeneRIF Biological Term Annotations	1.0	null
abnormality of the teeth	HPO Gene-Disease Associations	1.0	null
OVCAR433	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-0.978546
abnormality of the genital system	HPO Gene-Disease Associations	1.0	null
signs	GeneRIF Biological Term Annotations	1.0	null
partially	GeneRIF Biological Term Annotations	1.0	null
genome	GeneRIF Biological Term Annotations	1.0	null
only	GeneRIF Biological Term Annotations	1.0	null
abnormality of the gastrointestinal tract	HPO Gene-Disease Associations	1.0	null
abnormality of vision	HPO Gene-Disease Associations	1.0	null
behavioral abnormality	HPO Gene-Disease Associations	1.0	null
white	GeneRIF Biological Term Annotations	1.0	null
arterial stenosis	HPO Gene-Disease Associations	1.0	null
HCC202	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	1.21422
phenotypic abnormality	HPO Gene-Disease Associations	1.0	null
abnormal eye physiology	HPO Gene-Disease Associations	1.0	null
abnormality of skin morphology	HPO Gene-Disease Associations	1.0	null
abnormality of the abdomen	HPO Gene-Disease Associations	1.0	null
abnormal nervous system electrophysiology	HPO Gene-Disease Associations	1.0	null
abnormality of the choroid	HPO Gene-Disease Associations	1.0	null
OCI-AML5	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	2.12717
hypertension	GAD Gene-Disease Associations	1.0	null
oxidative	GeneRIF Biological Term Annotations	1.0	null
abnormality of hindbrain morphology	HPO Gene-Disease Associations	1.0	null
eeg abnormality	HPO Gene-Disease Associations	1.0	null
abnormality of the retina	HPO Gene-Disease Associations	1.0	null
nephrotic syndrome	HPO Gene-Disease Associations	1.0	null
abnormal bleeding	HPO Gene-Disease Associations	1.0	null
COLO 679	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	1.07456
short attention span	HPO Gene-Disease Associations	1.0	null
abnormality of skin pigmentation	HPO Gene-Disease Associations	1.0	null
spectrum	GeneRIF Biological Term Annotations	1.0	null
chain	GeneRIF Biological Term Annotations	1.0	null
abnormality of body weight	HPO Gene-Disease Associations	1.0	null
abnormality of the hypothalamus-pituitary axis	HPO Gene-Disease Associations	1.0	null
Spinocerebellar Degenerations	HuGE Navigator Gene-Phenotype Associations	1.0	null
intestinal obstruction	HPO Gene-Disease Associations	1.0	null
GTL-16	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-0.907287
variety	GeneRIF Biological Term Annotations	1.0	null
abnormality of the skin	HPO Gene-Disease Associations	1.0	null
Hypertrophy, Left Ventricular	HuGE Navigator Gene-Phenotype Associations	1.0	null
EB1	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	0.917473
eftu	GeneRIF Biological Term Annotations	1.0	null
HPAC	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	1.14765
MELAS Syndrome	HuGE Navigator Gene-Phenotype Associations	1.0	null
cerebral ischemia	HPO Gene-Disease Associations	1.0	null
deoxyribonucleic	GeneRIF Biological Term Annotations	1.0	null
abnormality of the metencephalon	HPO Gene-Disease Associations	1.0	null
Motor Neuron Disease	HuGE Navigator Gene-Phenotype Associations	1.0	null
abnormality of the outer ear	HPO Gene-Disease Associations	1.0	null
cerebral calcification	HPO Gene-Disease Associations	1.0	null
secretory	GeneRIF Biological Term Annotations	1.0	null
Diabetes Mellitus, Type 1	HuGE Navigator Gene-Phenotype Associations	1.0	null
doublepoint	GeneRIF Biological Term Annotations	1.0	null
Cerebrovascular Accident	HuGE Navigator Gene-Phenotype Associations	1.0	null
morphological abnormality of the central nervous system	HPO Gene-Disease Associations	1.0	null
abnormality of the lens	HPO Gene-Disease Associations	1.0	null
abnormality of the parathyroid gland	HPO Gene-Disease Associations	1.0	null
ageofonset	GeneRIF Biological Term Annotations	1.0	null
most	GeneRIF Biological Term Annotations	1.0	null
all	HPO Gene-Disease Associations	1.0	null
brain very small	HPO Gene-Disease Associations	1.0	null
inefficient	GeneRIF Biological Term Annotations	1.0	null
weakness due to upper motor neuron dysfunction	HPO Gene-Disease Associations	1.0	null
renal insufficiency	HPO Gene-Disease Associations	1.0	null
Mitochondrial Myopathies	HuGE Navigator Gene-Phenotype Associations	1.0	null
acid	GeneRIF Biological Term Annotations	1.0	null
abnormality of mitochondrial metabolism	HPO Gene-Disease Associations	1.0	null
classified	GeneRIF Biological Term Annotations	1.0	null
LCLC-103H	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-1.03356
T84	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	1.12691
Muscle Hypotonia	HuGE Navigator Gene-Phenotype Associations	1.0	null
phenotype	GeneRIF Biological Term Annotations	1.0	null
abnormality of the genitourinary system	HPO Gene-Disease Associations	1.0	null
pancreatitis	HPO Gene-Disease Associations	1.0	null
acidosis	GeneRIF Biological Term Annotations	1.0	null
amaurosis fugax	HPO Gene-Disease Associations	1.0	null
arrhythmia	HPO Gene-Disease Associations	1.0	null
autistic behavior	HPO Gene-Disease Associations	1.0	null
diabetes mellitus; werner syndrome	GAD Gene-Disease Associations	1.0	null
aplasia/hypoplasia involving the central nervous system	HPO Gene-Disease Associations	1.0	null
abnormality of the kidney	HPO Gene-Disease Associations	1.0	null
M059K	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-0.934599
Hearing Loss, Sensorineural	HuGE Navigator Gene-Phenotype Associations	1.0	null
Mitochondrial Encephalomyopathies	HuGE Navigator Gene-Phenotype Associations	1.0	null
JEKO-1	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	0.865676
abnormality of globe location	HPO Gene-Disease Associations	1.0	null
SW 780	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-1.12751
first	GeneRIF Biological Term Annotations	1.0	null
MT-3	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-1.07328
congestive heart failure	HPO Gene-Disease Associations	1.0	null
abnormality of muscle physiology	HPO Gene-Disease Associations	1.0	null
Muscular Diseases	HuGE Navigator Gene-Phenotype Associations	1.0	null
MDA-MB-157	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-1.35924
broadly	GeneRIF Biological Term Annotations	1.0	null
primary	GeneRIF Biological Term Annotations	1.0	null
abnormality of the oral cavity	HPO Gene-Disease Associations	1.0	null
NCI-H1435	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	2.34922
abnormality of head or neck	HPO Gene-Disease Associations	1.0	null
abnormality of the endocrine system	HPO Gene-Disease Associations	1.0	null
adverse	GeneRIF Biological Term Annotations	1.0	null
risk	GeneRIF Biological Term Annotations	1.0	null
intestinal pseudo-obstruction; mitochondrial diseases	GAD Gene-Disease Associations	1.0	null
structural	GeneRIF Biological Term Annotations	1.0	null
premature loss of teeth	HPO Gene-Disease Associations	1.0	null
abnormality of ion homeostasis	HPO Gene-Disease Associations	1.0	null
complexes	GeneRIF Biological Term Annotations	1.0	null
abnormality of metabolism/homeostasis	HPO Gene-Disease Associations	1.0	null
MERRF Syndrome	HuGE Navigator Gene-Phenotype Associations	1.0	null
ABC-1	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	0.854299
diabetes mellitus; glucose intolerance; muscular diseases	GAD Gene-Disease Associations	1.0	null
brain atrophy	HPO Gene-Disease Associations	1.0	null
abnormality of the anterior segment of the eye	HPO Gene-Disease Associations	1.0	null
aortic dissection	HPO Gene-Disease Associations	1.0	null
myalgia	HPO Gene-Disease Associations	1.0	null
SC-1	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	1.13578
abnormality of the immune system	HPO Gene-Disease Associations	1.0	null
abnormality of cell physiology	HPO Gene-Disease Associations	1.0	null
COLO 794	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-1.21896
HS 852.T	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	3.23814
emg abnormality	HPO Gene-Disease Associations	1.0	null
feeding difficulties	HPO Gene-Disease Associations	1.0	null
malformation of the heart and great vessels	HPO Gene-Disease Associations	1.0	null
abnormality of adipose tissue	HPO Gene-Disease Associations	1.0	null
deafness; diabetes mellitus; hearing loss, sensorineural; insulin resistance	GAD Gene-Disease Associations	1.0	null
cognitive impairment	HPO Gene-Disease Associations	1.0	null
KMS-11	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	1.47992
case	GeneRIF Biological Term Annotations	1.0	null
functional respiratory abnormality	HPO Gene-Disease Associations	1.0	null
cardiac arrest	HPO Gene-Disease Associations	1.0	null
hypoparathyroidism	HPO Gene-Disease Associations	1.0	null
KMS-28PE	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	0.995837
ichthyosis	HPO Gene-Disease Associations	1.0	null
hypertrichosis	HPO Gene-Disease Associations	1.0	null
dna	GeneRIF Biological Term Annotations	1.0	null
effects	GeneRIF Biological Term Annotations	1.0	null
tubular	GeneRIF Biological Term Annotations	1.0	null
Hypertension	HuGE Navigator Gene-Phenotype Associations	1.0	null
NCI-H1395	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	1.62777
type i diabetes mellitus	HPO Gene-Disease Associations	1.0	null
abnormality of muscle size	HPO Gene-Disease Associations	1.0	null
attention deficit hyperactivity disorder	HPO Gene-Disease Associations	1.0	null
aplasia/hypoplasia of the cerebrum	HPO Gene-Disease Associations	1.0	null
seizures	HPO Gene-Disease Associations	1.0	null
abnormality of the skeletal system	HPO Gene-Disease Associations	1.0	null
Genetic Predisposition to Disease	HuGE Navigator Gene-Phenotype Associations	1.0	null
SR	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-0.881979
abnormality of brain morphology	HPO Gene-Disease Associations	1.0	null
CAL-12T	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-0.883993
abnormality of the urinary system	HPO Gene-Disease Associations	1.0	null
deafness; diabetes mellitus	GAD Gene-Disease Associations	1.0	null
hyperthyroidism	HPO Gene-Disease Associations	1.0	null
Noninsulin-dependent diabetes mellitus with deafness	CTD Gene-Disease Associations	1.0	2.88009
Endometrial Neoplasms	HuGE Navigator Gene-Phenotype Associations	1.0	null
HS 578T	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-1.25692
insulin	GeneRIF Biological Term Annotations	1.0	null
primary adrenal insufficiency	HPO Gene-Disease Associations	1.0	null
abnormality of thyroid morphology	HPO Gene-Disease Associations	1.0	null
T-47D	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	-1.0	-1.17095
abnormality of skeletal physiology	HPO Gene-Disease Associations	1.0	null
aortic dilatation	HPO Gene-Disease Associations	1.0	null
blood	GeneRIF Biological Term Annotations	1.0	null
grades	GeneRIF Biological Term Annotations	1.0	null
KMS-34	Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles	1.0	0.955024
Child Development Disorders, Pervasive	HuGE Navigator Gene-Phenotype Associations	1.0	null
m3243agmttl1	GeneRIF Biological Term Annotations	1.0	null
abnormality of the ocular region	HPO Gene-Disease Associations	1.0	null
abnormality of immune system physiology	HPO Gene-Disease Associations	1.0	null
cleavage	GeneRIF Biological Term Annotations	1.0	null
Learning Disorders	HuGE Navigator Gene-Phenotype Associations	1.0	null
abnormality of blood and blood-forming tissues	HPO Gene-Disease Associations	1.0	null