Matches in Nanopublications for { ?s ?p "[A complex phenotype of peripheral neuropathy, myopathy, hoarseness, and hearing loss is linked to an autosomal dominant mutation in MYH14.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP616025.RAQ5hH07Bkf3oMjsfWJiDpk0E3pYmW0sh4sygIka5dAcc130_assertion description "[A complex phenotype of peripheral neuropathy, myopathy, hoarseness, and hearing loss is linked to an autosomal dominant mutation in MYH14.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP616025.RAQ5hH07Bkf3oMjsfWJiDpk0E3pYmW0sh4sygIka5dAcc130_provenance.
- NP4277.RAqy3nfDiIvy2hYiiEAbWxDHPE5dYWtA20NJkrHvKhzpY130_assertion description "[A complex phenotype of peripheral neuropathy, myopathy, hoarseness, and hearing loss is linked to an autosomal dominant mutation in MYH14.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4277.RAqy3nfDiIvy2hYiiEAbWxDHPE5dYWtA20NJkrHvKhzpY130_provenance.
- NP768119.RAwyIHQbb3wsbcVJ4lxz-r5B7JyP0g7vM8KFpXZKhpnDk130_assertion description "[A complex phenotype of peripheral neuropathy, myopathy, hoarseness, and hearing loss is linked to an autosomal dominant mutation in MYH14.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP768119.RAwyIHQbb3wsbcVJ4lxz-r5B7JyP0g7vM8KFpXZKhpnDk130_provenance.
- NP945574.RATNxE6zpN6hz-9GPof9PL8X6VLpQz9P3jgyju25ar7OU130_assertion description "[A complex phenotype of peripheral neuropathy, myopathy, hoarseness, and hearing loss is linked to an autosomal dominant mutation in MYH14.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP945574.RATNxE6zpN6hz-9GPof9PL8X6VLpQz9P3jgyju25ar7OU130_provenance.
- NP6599.RAadjMrBoJ8Hn3K5Rq1UBxgB8ZObbk_FZqJhCSE9ej3Hw130_assertion description "[A complex phenotype of peripheral neuropathy, myopathy, hoarseness, and hearing loss is linked to an autosomal dominant mutation in MYH14.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6599.RAadjMrBoJ8Hn3K5Rq1UBxgB8ZObbk_FZqJhCSE9ej3Hw130_provenance.
- assertion description "[A complex phenotype of peripheral neuropathy, myopathy, hoarseness, and hearing loss is linked to an autosomal dominant mutation in MYH14.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[A complex phenotype of peripheral neuropathy, myopathy, hoarseness, and hearing loss is linked to an autosomal dominant mutation in MYH14.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP886024.RAmg_o0xoaKn6dQY-i9eapn_oX_VcCTIxhTHJvIdQt6Dw130_assertion description "[A complex phenotype of peripheral neuropathy, myopathy, hoarseness, and hearing loss is linked to an autosomal dominant mutation in MYH14.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP886024.RAmg_o0xoaKn6dQY-i9eapn_oX_VcCTIxhTHJvIdQt6Dw130_provenance.
- NP932556.RAP0WYMS1DegHqi6X4d4DpN30_qnH9GKFkXBj8nLIq-NE130_assertion description "[A complex phenotype of peripheral neuropathy, myopathy, hoarseness, and hearing loss is linked to an autosomal dominant mutation in MYH14.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP932556.RAP0WYMS1DegHqi6X4d4DpN30_qnH9GKFkXBj8nLIq-NE130_provenance.
- NP886023.RAyzsKcz0yCqnMG3jhKQrwxiD6OTRvCLUn6-WTNPsUCfg130_assertion description "[A complex phenotype of peripheral neuropathy, myopathy, hoarseness, and hearing loss is linked to an autosomal dominant mutation in MYH14.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP886023.RAyzsKcz0yCqnMG3jhKQrwxiD6OTRvCLUn6-WTNPsUCfg130_provenance.