Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP635836.RAg5Qs-A2R2k7cZHtgSKGNXWSmzdgqelFutxdpGI0W0Ks130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP635836.RAg5Qs-A2R2k7cZHtgSKGNXWSmzdgqelFutxdpGI0W0Ks130_assertion type Assertion NP635836.RAg5Qs-A2R2k7cZHtgSKGNXWSmzdgqelFutxdpGI0W0Ks130_head.
- 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.