Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1108563.RA8VQMzUq1GOd2h6aDmwWqsappE0CCcdLmkTeKbRGBTSw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1108563.RA8VQMzUq1GOd2h6aDmwWqsappE0CCcdLmkTeKbRGBTSw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1108563.RA8VQMzUq1GOd2h6aDmwWqsappE0CCcdLmkTeKbRGBTSw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1108563.RA8VQMzUq1GOd2h6aDmwWqsappE0CCcdLmkTeKbRGBTSw130_provenance.
- NP1108563.RA8VQMzUq1GOd2h6aDmwWqsappE0CCcdLmkTeKbRGBTSw130_assertion description "[Here, we review the MYO5B gene and all currently known MYO5B mutations and for the first time methodologically categorize these with regard to functional protein domains and recurrence in MYO7A associated with Usher syndrome and other myosins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1108563.RA8VQMzUq1GOd2h6aDmwWqsappE0CCcdLmkTeKbRGBTSw130_provenance.
- NP1108563.RA8VQMzUq1GOd2h6aDmwWqsappE0CCcdLmkTeKbRGBTSw130_assertion evidence source_evidence_literature NP1108563.RA8VQMzUq1GOd2h6aDmwWqsappE0CCcdLmkTeKbRGBTSw130_provenance.
- NP1108563.RA8VQMzUq1GOd2h6aDmwWqsappE0CCcdLmkTeKbRGBTSw130_assertion SIO_000772 24014347 NP1108563.RA8VQMzUq1GOd2h6aDmwWqsappE0CCcdLmkTeKbRGBTSw130_provenance.
- NP1108563.RA8VQMzUq1GOd2h6aDmwWqsappE0CCcdLmkTeKbRGBTSw130_assertion wasDerivedFrom befree-2016 NP1108563.RA8VQMzUq1GOd2h6aDmwWqsappE0CCcdLmkTeKbRGBTSw130_provenance.
- NP1108563.RA8VQMzUq1GOd2h6aDmwWqsappE0CCcdLmkTeKbRGBTSw130_assertion wasGeneratedBy ECO_0000203 NP1108563.RA8VQMzUq1GOd2h6aDmwWqsappE0CCcdLmkTeKbRGBTSw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1108563.RA8VQMzUq1GOd2h6aDmwWqsappE0CCcdLmkTeKbRGBTSw130_provenance.