Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP635836.RAg5Qs-A2R2k7cZHtgSKGNXWSmzdgqelFutxdpGI0W0Ks130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP635836.RAg5Qs-A2R2k7cZHtgSKGNXWSmzdgqelFutxdpGI0W0Ks130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP635836.RAg5Qs-A2R2k7cZHtgSKGNXWSmzdgqelFutxdpGI0W0Ks130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP635836.RAg5Qs-A2R2k7cZHtgSKGNXWSmzdgqelFutxdpGI0W0Ks130_provenance.
- NP635836.RAg5Qs-A2R2k7cZHtgSKGNXWSmzdgqelFutxdpGI0W0Ks130_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." NP635836.RAg5Qs-A2R2k7cZHtgSKGNXWSmzdgqelFutxdpGI0W0Ks130_provenance.
- NP635836.RAg5Qs-A2R2k7cZHtgSKGNXWSmzdgqelFutxdpGI0W0Ks130_assertion evidence source_evidence_literature NP635836.RAg5Qs-A2R2k7cZHtgSKGNXWSmzdgqelFutxdpGI0W0Ks130_provenance.
- NP635836.RAg5Qs-A2R2k7cZHtgSKGNXWSmzdgqelFutxdpGI0W0Ks130_assertion SIO_000772 14585957 NP635836.RAg5Qs-A2R2k7cZHtgSKGNXWSmzdgqelFutxdpGI0W0Ks130_provenance.
- NP635836.RAg5Qs-A2R2k7cZHtgSKGNXWSmzdgqelFutxdpGI0W0Ks130_assertion wasDerivedFrom befree-20150227 NP635836.RAg5Qs-A2R2k7cZHtgSKGNXWSmzdgqelFutxdpGI0W0Ks130_provenance.
- NP635836.RAg5Qs-A2R2k7cZHtgSKGNXWSmzdgqelFutxdpGI0W0Ks130_assertion wasGeneratedBy ECO_0000203 NP635836.RAg5Qs-A2R2k7cZHtgSKGNXWSmzdgqelFutxdpGI0W0Ks130_provenance.
- befree-20150227 importedOn "2015-02-27" NP635836.RAg5Qs-A2R2k7cZHtgSKGNXWSmzdgqelFutxdpGI0W0Ks130_provenance.