Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP584095.RA33EOBNQgSWrrt5JyhadlcmCX9khbDBykhR892TumkoI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP584095.RA33EOBNQgSWrrt5JyhadlcmCX9khbDBykhR892TumkoI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP584095.RA33EOBNQgSWrrt5JyhadlcmCX9khbDBykhR892TumkoI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP584095.RA33EOBNQgSWrrt5JyhadlcmCX9khbDBykhR892TumkoI130_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.
- 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.
- befree-20150227 importedOn "2015-02-27" NP584095.RA33EOBNQgSWrrt5JyhadlcmCX9khbDBykhR892TumkoI130_provenance.