Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP418722.RA7ECDsAB42sHcQaRPVgd5GJgeKD1csFehYR2cU2uxEvg130_assertion> ?p ?o ?g. }
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- NP418722.RA7ECDsAB42sHcQaRPVgd5GJgeKD1csFehYR2cU2uxEvg130_assertion type Assertion NP418722.RA7ECDsAB42sHcQaRPVgd5GJgeKD1csFehYR2cU2uxEvg130_head.
- NP418722.RA7ECDsAB42sHcQaRPVgd5GJgeKD1csFehYR2cU2uxEvg130_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." NP418722.RA7ECDsAB42sHcQaRPVgd5GJgeKD1csFehYR2cU2uxEvg130_provenance.
- NP418722.RA7ECDsAB42sHcQaRPVgd5GJgeKD1csFehYR2cU2uxEvg130_assertion evidence source_evidence_literature NP418722.RA7ECDsAB42sHcQaRPVgd5GJgeKD1csFehYR2cU2uxEvg130_provenance.
- NP418722.RA7ECDsAB42sHcQaRPVgd5GJgeKD1csFehYR2cU2uxEvg130_assertion SIO_000772 14585957 NP418722.RA7ECDsAB42sHcQaRPVgd5GJgeKD1csFehYR2cU2uxEvg130_provenance.
- NP418722.RA7ECDsAB42sHcQaRPVgd5GJgeKD1csFehYR2cU2uxEvg130_assertion wasDerivedFrom befree-2016 NP418722.RA7ECDsAB42sHcQaRPVgd5GJgeKD1csFehYR2cU2uxEvg130_provenance.
- NP418722.RA7ECDsAB42sHcQaRPVgd5GJgeKD1csFehYR2cU2uxEvg130_assertion wasGeneratedBy ECO_0000203 NP418722.RA7ECDsAB42sHcQaRPVgd5GJgeKD1csFehYR2cU2uxEvg130_provenance.