Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP692360.RAb_P0Jj5Wna3DeTPOPW6VVKu-WV4-83kEhTlbOObuUFA130_assertion> ?p ?o ?g. }
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- NP692360.RAb_P0Jj5Wna3DeTPOPW6VVKu-WV4-83kEhTlbOObuUFA130_assertion type Assertion NP692360.RAb_P0Jj5Wna3DeTPOPW6VVKu-WV4-83kEhTlbOObuUFA130_head.
- NP692360.RAb_P0Jj5Wna3DeTPOPW6VVKu-WV4-83kEhTlbOObuUFA130_assertion description "[A mutation in the POU4F3 gene (BRN-3.1, BRN3C) is responsible for DFNA15 (MIM 602459), autosomal-dominant nonsyndromic hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP692360.RAb_P0Jj5Wna3DeTPOPW6VVKu-WV4-83kEhTlbOObuUFA130_provenance.
- NP692360.RAb_P0Jj5Wna3DeTPOPW6VVKu-WV4-83kEhTlbOObuUFA130_assertion evidence source_evidence_literature NP692360.RAb_P0Jj5Wna3DeTPOPW6VVKu-WV4-83kEhTlbOObuUFA130_provenance.
- NP692360.RAb_P0Jj5Wna3DeTPOPW6VVKu-WV4-83kEhTlbOObuUFA130_assertion SIO_000772 14585957 NP692360.RAb_P0Jj5Wna3DeTPOPW6VVKu-WV4-83kEhTlbOObuUFA130_provenance.
- NP692360.RAb_P0Jj5Wna3DeTPOPW6VVKu-WV4-83kEhTlbOObuUFA130_assertion wasDerivedFrom befree-20140225 NP692360.RAb_P0Jj5Wna3DeTPOPW6VVKu-WV4-83kEhTlbOObuUFA130_provenance.
- NP692360.RAb_P0Jj5Wna3DeTPOPW6VVKu-WV4-83kEhTlbOObuUFA130_assertion wasGeneratedBy ECO_0000203 NP692360.RAb_P0Jj5Wna3DeTPOPW6VVKu-WV4-83kEhTlbOObuUFA130_provenance.