Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP655909.RAU5wdr9-7g4EUlJCDq5Xm6e0WrmTXw_388hQoCenXO18130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP655909.RAU5wdr9-7g4EUlJCDq5Xm6e0WrmTXw_388hQoCenXO18130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP655909.RAU5wdr9-7g4EUlJCDq5Xm6e0WrmTXw_388hQoCenXO18130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP655909.RAU5wdr9-7g4EUlJCDq5Xm6e0WrmTXw_388hQoCenXO18130_provenance.
- NP655909.RAU5wdr9-7g4EUlJCDq5Xm6e0WrmTXw_388hQoCenXO18130_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." NP655909.RAU5wdr9-7g4EUlJCDq5Xm6e0WrmTXw_388hQoCenXO18130_provenance.
- NP655909.RAU5wdr9-7g4EUlJCDq5Xm6e0WrmTXw_388hQoCenXO18130_assertion evidence source_evidence_literature NP655909.RAU5wdr9-7g4EUlJCDq5Xm6e0WrmTXw_388hQoCenXO18130_provenance.
- NP655909.RAU5wdr9-7g4EUlJCDq5Xm6e0WrmTXw_388hQoCenXO18130_assertion SIO_000772 21326233 NP655909.RAU5wdr9-7g4EUlJCDq5Xm6e0WrmTXw_388hQoCenXO18130_provenance.
- NP655909.RAU5wdr9-7g4EUlJCDq5Xm6e0WrmTXw_388hQoCenXO18130_assertion wasDerivedFrom befree-20140225 NP655909.RAU5wdr9-7g4EUlJCDq5Xm6e0WrmTXw_388hQoCenXO18130_provenance.
- NP655909.RAU5wdr9-7g4EUlJCDq5Xm6e0WrmTXw_388hQoCenXO18130_assertion wasGeneratedBy ECO_0000203 NP655909.RAU5wdr9-7g4EUlJCDq5Xm6e0WrmTXw_388hQoCenXO18130_provenance.
- befree-20140225 importedOn "2014-02-25" NP655909.RAU5wdr9-7g4EUlJCDq5Xm6e0WrmTXw_388hQoCenXO18130_provenance.