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- source_evidence_literature type ECO_0000212 NP692360.RAb_P0Jj5Wna3DeTPOPW6VVKu-WV4-83kEhTlbOObuUFA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP692360.RAb_P0Jj5Wna3DeTPOPW6VVKu-WV4-83kEhTlbOObuUFA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP692360.RAb_P0Jj5Wna3DeTPOPW6VVKu-WV4-83kEhTlbOObuUFA130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP692360.RAb_P0Jj5Wna3DeTPOPW6VVKu-WV4-83kEhTlbOObuUFA130_provenance.