Matches in Nanopublications for { ?s ?p "[the first description of a mutation in cytoskeletal, or nonmuscle, actin; with an autosomal dominant, progressive, sensorineural hearing loss phenotype ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP136191.RA9YAZSEeNKAlqAL37WGkry9LUBC-H1JJ4hIADDooJV6I130_assertion description "[the first description of a mutation in cytoskeletal, or nonmuscle, actin; with an autosomal dominant, progressive, sensorineural hearing loss phenotype ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136191.RA9YAZSEeNKAlqAL37WGkry9LUBC-H1JJ4hIADDooJV6I130_provenance.
- NP199345.RAGyx1oiR3cUQDTvpVHlBluJF1JIPK_C7Ihe0EpUOpJHs130_assertion description "[the first description of a mutation in cytoskeletal, or nonmuscle, actin; with an autosomal dominant, progressive, sensorineural hearing loss phenotype ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199345.RAGyx1oiR3cUQDTvpVHlBluJF1JIPK_C7Ihe0EpUOpJHs130_provenance.
- NP201460.RAyEwKlWc3VCIs0BR2Zo8AIIHMRmJPQP7-tyEcNajMrf8130_assertion description "[the first description of a mutation in cytoskeletal, or nonmuscle, actin; with an autosomal dominant, progressive, sensorineural hearing loss phenotype ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP201460.RAyEwKlWc3VCIs0BR2Zo8AIIHMRmJPQP7-tyEcNajMrf8130_provenance.