Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP156184.RACv3qJpxstktqZi9AcsU0xfI3MD355mZ6uiitT1xWgT4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP156184.RACv3qJpxstktqZi9AcsU0xfI3MD355mZ6uiitT1xWgT4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP156184.RACv3qJpxstktqZi9AcsU0xfI3MD355mZ6uiitT1xWgT4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP156184.RACv3qJpxstktqZi9AcsU0xfI3MD355mZ6uiitT1xWgT4130_provenance.
- NP156184.RACv3qJpxstktqZi9AcsU0xfI3MD355mZ6uiitT1xWgT4130_assertion description "[Seven missense mutations and one in-frame deletion mutation have been reported in the coagulation factor C homology (COCH) gene, causing the adult-onset, progressive sensorineural hearing loss and vestibular disorder at the DFNA9 locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP156184.RACv3qJpxstktqZi9AcsU0xfI3MD355mZ6uiitT1xWgT4130_provenance.
- NP156184.RACv3qJpxstktqZi9AcsU0xfI3MD355mZ6uiitT1xWgT4130_assertion evidence source_evidence_literature NP156184.RACv3qJpxstktqZi9AcsU0xfI3MD355mZ6uiitT1xWgT4130_provenance.
- NP156184.RACv3qJpxstktqZi9AcsU0xfI3MD355mZ6uiitT1xWgT4130_assertion SIO_000772 16481359 NP156184.RACv3qJpxstktqZi9AcsU0xfI3MD355mZ6uiitT1xWgT4130_provenance.
- NP156184.RACv3qJpxstktqZi9AcsU0xfI3MD355mZ6uiitT1xWgT4130_assertion wasDerivedFrom befree-20140225 NP156184.RACv3qJpxstktqZi9AcsU0xfI3MD355mZ6uiitT1xWgT4130_provenance.
- NP156184.RACv3qJpxstktqZi9AcsU0xfI3MD355mZ6uiitT1xWgT4130_assertion wasGeneratedBy ECO_0000203 NP156184.RACv3qJpxstktqZi9AcsU0xfI3MD355mZ6uiitT1xWgT4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP156184.RACv3qJpxstktqZi9AcsU0xfI3MD355mZ6uiitT1xWgT4130_provenance.