Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP455521.RA4ruzn3ru2ITzp9dg5vCWzZlzSbs7KXcWzULa-XsZAIA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP455521.RA4ruzn3ru2ITzp9dg5vCWzZlzSbs7KXcWzULa-XsZAIA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP455521.RA4ruzn3ru2ITzp9dg5vCWzZlzSbs7KXcWzULa-XsZAIA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP455521.RA4ruzn3ru2ITzp9dg5vCWzZlzSbs7KXcWzULa-XsZAIA130_provenance.
- NP455521.RA4ruzn3ru2ITzp9dg5vCWzZlzSbs7KXcWzULa-XsZAIA130_assertion description "[OCA3 (MIM 203290), a rare form of OCA and also known as `rufous/red albinism,` is associated with mutations in TYRP1 (encoding tyrosinase-related protein 1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP455521.RA4ruzn3ru2ITzp9dg5vCWzZlzSbs7KXcWzULa-XsZAIA130_provenance.
- NP455521.RA4ruzn3ru2ITzp9dg5vCWzZlzSbs7KXcWzULa-XsZAIA130_assertion evidence source_evidence_literature NP455521.RA4ruzn3ru2ITzp9dg5vCWzZlzSbs7KXcWzULa-XsZAIA130_provenance.
- NP455521.RA4ruzn3ru2ITzp9dg5vCWzZlzSbs7KXcWzULa-XsZAIA130_assertion SIO_000772 11574907 NP455521.RA4ruzn3ru2ITzp9dg5vCWzZlzSbs7KXcWzULa-XsZAIA130_provenance.
- NP455521.RA4ruzn3ru2ITzp9dg5vCWzZlzSbs7KXcWzULa-XsZAIA130_assertion wasDerivedFrom befree-20140225 NP455521.RA4ruzn3ru2ITzp9dg5vCWzZlzSbs7KXcWzULa-XsZAIA130_provenance.
- NP455521.RA4ruzn3ru2ITzp9dg5vCWzZlzSbs7KXcWzULa-XsZAIA130_assertion wasGeneratedBy ECO_0000203 NP455521.RA4ruzn3ru2ITzp9dg5vCWzZlzSbs7KXcWzULa-XsZAIA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP455521.RA4ruzn3ru2ITzp9dg5vCWzZlzSbs7KXcWzULa-XsZAIA130_provenance.