Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP280989.RAkppUmaH2xHyTlArG62agfTIBskSiIooGbUxp5uClvck130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP280989.RAkppUmaH2xHyTlArG62agfTIBskSiIooGbUxp5uClvck130_assertion type Assertion NP280989.RAkppUmaH2xHyTlArG62agfTIBskSiIooGbUxp5uClvck130_head.
- 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.