Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP280989.RAkppUmaH2xHyTlArG62agfTIBskSiIooGbUxp5uClvck130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP280989.RAkppUmaH2xHyTlArG62agfTIBskSiIooGbUxp5uClvck130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP280989.RAkppUmaH2xHyTlArG62agfTIBskSiIooGbUxp5uClvck130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP280989.RAkppUmaH2xHyTlArG62agfTIBskSiIooGbUxp5uClvck130_provenance.
- NP280989.RAkppUmaH2xHyTlArG62agfTIBskSiIooGbUxp5uClvck130_assertion description "[Mutations in the connexin 26 (Cx26) or gap junction beta 2 gene are the leading cause of hereditary nonsyndromic sensorineural hearing loss in Caucasians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP280989.RAkppUmaH2xHyTlArG62agfTIBskSiIooGbUxp5uClvck130_provenance.
- NP280989.RAkppUmaH2xHyTlArG62agfTIBskSiIooGbUxp5uClvck130_assertion evidence source_evidence_literature NP280989.RAkppUmaH2xHyTlArG62agfTIBskSiIooGbUxp5uClvck130_provenance.
- NP280989.RAkppUmaH2xHyTlArG62agfTIBskSiIooGbUxp5uClvck130_assertion SIO_000772 15064611 NP280989.RAkppUmaH2xHyTlArG62agfTIBskSiIooGbUxp5uClvck130_provenance.
- NP280989.RAkppUmaH2xHyTlArG62agfTIBskSiIooGbUxp5uClvck130_assertion wasDerivedFrom befree-20140225 NP280989.RAkppUmaH2xHyTlArG62agfTIBskSiIooGbUxp5uClvck130_provenance.
- NP280989.RAkppUmaH2xHyTlArG62agfTIBskSiIooGbUxp5uClvck130_assertion wasGeneratedBy ECO_0000203 NP280989.RAkppUmaH2xHyTlArG62agfTIBskSiIooGbUxp5uClvck130_provenance.
- befree-20140225 importedOn "2014-02-25" NP280989.RAkppUmaH2xHyTlArG62agfTIBskSiIooGbUxp5uClvck130_provenance.