Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP183919.RACiPPBLtVw4wWGAWS5zXrXaIy9_Rmu4EITM5ei49iedo130_assertion> ?p ?o ?g. }
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- NP183919.RACiPPBLtVw4wWGAWS5zXrXaIy9_Rmu4EITM5ei49iedo130_assertion type Assertion NP183919.RACiPPBLtVw4wWGAWS5zXrXaIy9_Rmu4EITM5ei49iedo130_head.
- NP183919.RACiPPBLtVw4wWGAWS5zXrXaIy9_Rmu4EITM5ei49iedo130_assertion description "[Mutant POU4F3 loses most of its transcriptional activity and most of its ability to bind to DNA/mutation causes autosomal-dominant nonsyndromic hearing loss and eventually leads to hair cell morbidity in affected family H members.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP183919.RACiPPBLtVw4wWGAWS5zXrXaIy9_Rmu4EITM5ei49iedo130_provenance.
- NP183919.RACiPPBLtVw4wWGAWS5zXrXaIy9_Rmu4EITM5ei49iedo130_assertion evidence source_evidence_literature NP183919.RACiPPBLtVw4wWGAWS5zXrXaIy9_Rmu4EITM5ei49iedo130_provenance.
- NP183919.RACiPPBLtVw4wWGAWS5zXrXaIy9_Rmu4EITM5ei49iedo130_assertion SIO_000772 14585957 NP183919.RACiPPBLtVw4wWGAWS5zXrXaIy9_Rmu4EITM5ei49iedo130_provenance.
- NP183919.RACiPPBLtVw4wWGAWS5zXrXaIy9_Rmu4EITM5ei49iedo130_assertion wasDerivedFrom lhgdn-20090331 NP183919.RACiPPBLtVw4wWGAWS5zXrXaIy9_Rmu4EITM5ei49iedo130_provenance.
- NP183919.RACiPPBLtVw4wWGAWS5zXrXaIy9_Rmu4EITM5ei49iedo130_assertion wasGeneratedBy ECO_0000203 NP183919.RACiPPBLtVw4wWGAWS5zXrXaIy9_Rmu4EITM5ei49iedo130_provenance.