Matches in Nanopublications for { ?s ?p "[Usher syndromeIb (USH1B), an autosomal recessive disorder caused by mutations in myosin VIIa (MYO7A), is characterized by congenital profound hearing loss, vestibular abnormalities and retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 11 of
11
with 100 items per page.
- NP506357.RAlTeBqTcnTpJwpr6Z_Wg5PDEhzA0kdpeNvUxtvEr7Hio130_assertion description "[Usher syndromeIb (USH1B), an autosomal recessive disorder caused by mutations in myosin VIIa (MYO7A), is characterized by congenital profound hearing loss, vestibular abnormalities and retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP506357.RAlTeBqTcnTpJwpr6Z_Wg5PDEhzA0kdpeNvUxtvEr7Hio130_provenance.
- NP494147.RAWT9Jimiq-PniUc87kUUJXSvT9E7QqYYPXYLKbgz-Rhw130_assertion description "[Usher syndromeIb (USH1B), an autosomal recessive disorder caused by mutations in myosin VIIa (MYO7A), is characterized by congenital profound hearing loss, vestibular abnormalities and retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP494147.RAWT9Jimiq-PniUc87kUUJXSvT9E7QqYYPXYLKbgz-Rhw130_provenance.
- assertion description "[Usher syndromeIb (USH1B), an autosomal recessive disorder caused by mutations in myosin VIIa (MYO7A), is characterized by congenital profound hearing loss, vestibular abnormalities and retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Usher syndromeIb (USH1B), an autosomal recessive disorder caused by mutations in myosin VIIa (MYO7A), is characterized by congenital profound hearing loss, vestibular abnormalities and retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP271069.RAUf76UaGX2D7CzqRqAwP4lz3hmJhSPPUniWVRzp-t-gU130_assertion description "[Usher syndromeIb (USH1B), an autosomal recessive disorder caused by mutations in myosin VIIa (MYO7A), is characterized by congenital profound hearing loss, vestibular abnormalities and retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP271069.RAUf76UaGX2D7CzqRqAwP4lz3hmJhSPPUniWVRzp-t-gU130_provenance.
- NP264321.RAAE_KyabMXvECVElSCspw9V3hImnZlWDXxiLpBdzSXCg130_assertion description "[Usher syndromeIb (USH1B), an autosomal recessive disorder caused by mutations in myosin VIIa (MYO7A), is characterized by congenital profound hearing loss, vestibular abnormalities and retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP264321.RAAE_KyabMXvECVElSCspw9V3hImnZlWDXxiLpBdzSXCg130_provenance.
- NP264322.RAV1HEk_OpSxKqf9-DwCRbWNcoqJE1z9gfa9m6fodWFto130_assertion description "[Usher syndromeIb (USH1B), an autosomal recessive disorder caused by mutations in myosin VIIa (MYO7A), is characterized by congenital profound hearing loss, vestibular abnormalities and retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP264322.RAV1HEk_OpSxKqf9-DwCRbWNcoqJE1z9gfa9m6fodWFto130_provenance.
- NP271070.RAmPtj0L39EfgEmxb_qu4kx-r3Nw6B9W1B_t40R6gQhc4130_assertion description "[Usher syndromeIb (USH1B), an autosomal recessive disorder caused by mutations in myosin VIIa (MYO7A), is characterized by congenital profound hearing loss, vestibular abnormalities and retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP271070.RAmPtj0L39EfgEmxb_qu4kx-r3Nw6B9W1B_t40R6gQhc4130_provenance.
- NP584102.RAPt744UTjGhY8Wyu5WjUuApoi_inNjv7xXxZlubZcIuI130_assertion description "[Usher syndromeIb (USH1B), an autosomal recessive disorder caused by mutations in myosin VIIa (MYO7A), is characterized by congenital profound hearing loss, vestibular abnormalities and retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP584102.RAPt744UTjGhY8Wyu5WjUuApoi_inNjv7xXxZlubZcIuI130_provenance.
- NP584095.RA33EOBNQgSWrrt5JyhadlcmCX9khbDBykhR892TumkoI130_assertion description "[Usher syndromeIb (USH1B), an autosomal recessive disorder caused by mutations in myosin VIIa (MYO7A), is characterized by congenital profound hearing loss, vestibular abnormalities and retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP584095.RA33EOBNQgSWrrt5JyhadlcmCX9khbDBykhR892TumkoI130_provenance.
- NP584096.RA1Iaw-Q4UTaen5HLBn776kL2Jd4jKGfP3gyEv0ICXCRQ130_assertion description "[Usher syndromeIb (USH1B), an autosomal recessive disorder caused by mutations in myosin VIIa (MYO7A), is characterized by congenital profound hearing loss, vestibular abnormalities and retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP584096.RA1Iaw-Q4UTaen5HLBn776kL2Jd4jKGfP3gyEv0ICXCRQ130_provenance.