association	dataset	threshold value	standardized value
neurological	GAD High Level Gene-Disease Associations	1.0	0.298214
fraxa	GeneRIF Biological Term Annotations	1.0	null
normal	GeneRIF Biological Term Annotations	1.0	null
spinocerebellar ataxia	GAD Gene-Disease Associations	1.0	null
indistinguishable	GeneRIF Biological Term Annotations	1.0	null
repeats	GeneRIF Biological Term Annotations	1.0	null
distribution	GeneRIF Biological Term Annotations	1.0	null
different	GeneRIF Biological Term Annotations	1.0	null
Fragile X Syndrome	HuGE Navigator Gene-Phenotype Associations	1.0	null
Mental Retardation	HuGE Navigator Gene-Phenotype Associations	1.0	null
other	GAD High Level Gene-Disease Associations	1.0	0.298214
groups	GeneRIF Biological Term Annotations	1.0	null
triplets	GeneRIF Biological Term Annotations	1.0	null
Mental Retardation, X-Linked	HuGE Navigator Gene-Phenotype Associations	1.0	null
haplotype	GeneRIF Biological Term Annotations	1.0	null
reported	GeneRIF Biological Term Annotations	1.0	null
fragile x syndrome	GAD Gene-Disease Associations	1.0	null
psych	GAD High Level Gene-Disease Associations	1.0	0.298214
showing	GeneRIF Biological Term Annotations	1.0	null
families	GeneRIF Biological Term Annotations	1.0	null
essential tremor; cerebral ataxia; multiple-system atropy; parkinsonism	GAD Gene-Disease Associations	1.0	null
reproduction	GAD High Level Gene-Disease Associations	1.0	0.298214
Myotonic Dystrophy	HuGE Navigator Gene-Phenotype Associations	1.0	null
alleles	GeneRIF Biological Term Annotations	1.0	null
showed	GeneRIF Biological Term Annotations	1.0	null
premature ovarian failure	GAD Gene-Disease Associations	1.0	null
Autistic Disorder	HuGE Navigator Gene-Phenotype Associations	1.0	null
linkage	GeneRIF Biological Term Annotations	1.0	null
dyslexia	GeneRIF Biological Term Annotations	1.0	null
manifestations	GeneRIF Biological Term Annotations	1.0	null
quadruplexforming	GeneRIF Biological Term Annotations	1.0	null
cgg	GeneRIF Biological Term Annotations	1.0	null
fragile x syndrome; periodontitis	GAD Gene-Disease Associations	1.0	null
founder	GeneRIF Biological Term Annotations	1.0	null
Friedreich Ataxia	HuGE Navigator Gene-Phenotype Associations	1.0	null
Ovarian Failure, Premature	HuGE Navigator Gene-Phenotype Associations	1.0	null
french	GeneRIF Biological Term Annotations	1.0	null
Muscular Atrophy, Spinal	HuGE Navigator Gene-Phenotype Associations	1.0	null
allele	GeneRIF Biological Term Annotations	1.0	null
Menopause, Premature	HuGE Navigator Gene-Phenotype Associations	1.0	null
clinical	GeneRIF Biological Term Annotations	1.0	null
effect	GeneRIF Biological Term Annotations	1.0	null
Interview, Psychological	HuGE Navigator Gene-Phenotype Associations	1.0	null
multiple system atrophy	GAD Gene-Disease Associations	1.0	null
Movement Disorders	HuGE Navigator Gene-Phenotype Associations	1.0	null
parkinsons	GeneRIF Biological Term Annotations	1.0	null
Multiple System Atrophy	HuGE Navigator Gene-Phenotype Associations	1.0	null
fragile	GeneRIF Biological Term Annotations	1.0	null
agg	GeneRIF Biological Term Annotations	1.0	null
suggesting	GeneRIF Biological Term Annotations	1.0	null
controls	GeneRIF Biological Term Annotations	1.0	null
Spinocerebellar Ataxias	HuGE Navigator Gene-Phenotype Associations	1.0	null
Wechsler Scales	HuGE Navigator Gene-Phenotype Associations	1.0	null
schizophrenia	GAD Gene-Disease Associations	1.0	null
carrying	GeneRIF Biological Term Annotations	1.0	null
triplet repeat expansion at fraxa and fraxe	GAD Gene-Disease Associations	1.0	null
properties	GeneRIF Biological Term Annotations	1.0	null
Essential Tremor	HuGE Navigator Gene-Phenotype Associations	1.0	null
interrupted	GeneRIF Biological Term Annotations	1.0	null
idiopathic	GeneRIF Biological Term Annotations	1.0	null
Parkinson Disease	HuGE Navigator Gene-Phenotype Associations	1.0	null
parkinson's disease	GAD Gene-Disease Associations	1.0	null
myotonic dystrophy type 1	GAD Gene-Disease Associations	1.0	null
premutation	GeneRIF Biological Term Annotations	1.0	null
finding	GeneRIF Biological Term Annotations	1.0	null
Asperger Syndrome	HuGE Navigator Gene-Phenotype Associations	1.0	null
autism; asperger syndrome	GAD Gene-Disease Associations	1.0	null
fragile x syndrome; fragile x syndromes; mental retardation	GAD Gene-Disease Associations	1.0	null
developmental	GAD High Level Gene-Disease Associations	1.0	0.321139
Cerebellar Ataxia	HuGE Navigator Gene-Phenotype Associations	1.0	null
significant	GeneRIF Biological Term Annotations	1.0	null
weak	GeneRIF Biological Term Annotations	1.0	null
Schizophrenia	HuGE Navigator Gene-Phenotype Associations	1.0	null
Genetic Predisposition to Disease	HuGE Navigator Gene-Phenotype Associations	1.0	null