paralytic poliomyelitis Gene Set

Dataset	DISEASES Text-mining Gene-Disease Association Evidence Scores
Category	disease or phenotype associations
Type	disease
Description	A poliomyelitis that results_in destruction located_in motor neurons of central nervous system, has_material_basis_in Human poliovirus 1, has_material_basis_in Human poliovirus 2, or has_material_basis_in Human poliovirus 3, which are transmitted_by ingestion of food or water contaminated with feces, or transmitted_by direct contact with the oral secretions. The infection has_symptom loss of reflexes, has_symptom muscle spasms, and has_symptom acute flaccid paralysis. (Human Disease Ontology, DOID_0050515)
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Genes

19 genes co-occuring with the disease paralytic poliomyelitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol	Name	Standardized Value
PVR	poliovirus receptor	2.35924
DPT	dermatopontin	1.51325
ARHGEF1	Rho guanine nucleotide exchange factor (GEF) 1	1.18971
KHSRP	KH-type splicing regulatory protein	1.03367
SLC50A1	solute carrier family 50 (sugar efflux transporter), member 1	0.841344
IFIH1	interferon induced with helicase C domain 1	0.711183
BTK	Bruton agammaglobulinemia tyrosine kinase	0.692296
NTSR1	neurotensin receptor 1 (high affinity)	0.610448
CD79A	CD79a molecule, immunoglobulin-associated alpha	0.474498
LIG3	ligase III, DNA, ATP-dependent	0.467684
MLN	motilin	0.453716
HLA-A	major histocompatibility complex, class I, A	0.337242
TLR7	toll-like receptor 7	0.329565
APOLD1	apolipoprotein L domain containing 1	0.325187
ERVW-1	endogenous retrovirus group W, member 1	0.299812
TLR3	toll-like receptor 3	0.283297
CHAT	choline O-acetyltransferase	0.253479
MRAP	melanocortin 2 receptor accessory protein	0.220424
PTPN11	protein tyrosine phosphatase, non-receptor type 11	0.161139