Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP872955.RA4Bjad7QwhCb17w3uxXyg1qEcLPKZcq6Bg5byx-LsXtY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP872955.RA4Bjad7QwhCb17w3uxXyg1qEcLPKZcq6Bg5byx-LsXtY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP872955.RA4Bjad7QwhCb17w3uxXyg1qEcLPKZcq6Bg5byx-LsXtY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP872955.RA4Bjad7QwhCb17w3uxXyg1qEcLPKZcq6Bg5byx-LsXtY130_provenance.
- NP872955.RA4Bjad7QwhCb17w3uxXyg1qEcLPKZcq6Bg5byx-LsXtY130_assertion description "[Here, we identify mutations in Gipc3 underlying progressive sensorineural hearing loss (age-related hearing loss 5, ahl5) and audiogenic seizures (juvenile audiogenic monogenic seizure 1, jams1) in mice and autosomal recessive deafness DFNB15 and DFNB95 in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP872955.RA4Bjad7QwhCb17w3uxXyg1qEcLPKZcq6Bg5byx-LsXtY130_provenance.
- NP872955.RA4Bjad7QwhCb17w3uxXyg1qEcLPKZcq6Bg5byx-LsXtY130_assertion evidence source_evidence_literature NP872955.RA4Bjad7QwhCb17w3uxXyg1qEcLPKZcq6Bg5byx-LsXtY130_provenance.
- NP872955.RA4Bjad7QwhCb17w3uxXyg1qEcLPKZcq6Bg5byx-LsXtY130_assertion SIO_000772 21326233 NP872955.RA4Bjad7QwhCb17w3uxXyg1qEcLPKZcq6Bg5byx-LsXtY130_provenance.
- NP872955.RA4Bjad7QwhCb17w3uxXyg1qEcLPKZcq6Bg5byx-LsXtY130_assertion wasDerivedFrom befree-2016 NP872955.RA4Bjad7QwhCb17w3uxXyg1qEcLPKZcq6Bg5byx-LsXtY130_provenance.
- NP872955.RA4Bjad7QwhCb17w3uxXyg1qEcLPKZcq6Bg5byx-LsXtY130_assertion wasGeneratedBy ECO_0000203 NP872955.RA4Bjad7QwhCb17w3uxXyg1qEcLPKZcq6Bg5byx-LsXtY130_provenance.
- befree-2016 importedOn "2016-02-19" NP872955.RA4Bjad7QwhCb17w3uxXyg1qEcLPKZcq6Bg5byx-LsXtY130_provenance.