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- NP584095.RA33EOBNQgSWrrt5JyhadlcmCX9khbDBykhR892TumkoI130_assertion type Assertion NP584095.RA33EOBNQgSWrrt5JyhadlcmCX9khbDBykhR892TumkoI130_head.
- 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.
- NP584095.RA33EOBNQgSWrrt5JyhadlcmCX9khbDBykhR892TumkoI130_assertion evidence source_evidence_literature NP584095.RA33EOBNQgSWrrt5JyhadlcmCX9khbDBykhR892TumkoI130_provenance.
- NP584095.RA33EOBNQgSWrrt5JyhadlcmCX9khbDBykhR892TumkoI130_assertion SIO_000772 10502787 NP584095.RA33EOBNQgSWrrt5JyhadlcmCX9khbDBykhR892TumkoI130_provenance.
- NP584095.RA33EOBNQgSWrrt5JyhadlcmCX9khbDBykhR892TumkoI130_assertion wasDerivedFrom befree-20150227 NP584095.RA33EOBNQgSWrrt5JyhadlcmCX9khbDBykhR892TumkoI130_provenance.
- NP584095.RA33EOBNQgSWrrt5JyhadlcmCX9khbDBykhR892TumkoI130_assertion wasGeneratedBy ECO_0000203 NP584095.RA33EOBNQgSWrrt5JyhadlcmCX9khbDBykhR892TumkoI130_provenance.