Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- 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.
- 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." 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.
- 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.