Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1248487.RA5x0tzdMooOhdQY8gVKSUGgpsT4zcjq9WEvxQssaYsGA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1248487.RA5x0tzdMooOhdQY8gVKSUGgpsT4zcjq9WEvxQssaYsGA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1248487.RA5x0tzdMooOhdQY8gVKSUGgpsT4zcjq9WEvxQssaYsGA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1248487.RA5x0tzdMooOhdQY8gVKSUGgpsT4zcjq9WEvxQssaYsGA130_provenance.
- NP1248487.RA5x0tzdMooOhdQY8gVKSUGgpsT4zcjq9WEvxQssaYsGA130_assertion description "[The most common form of albinism is caused by mutations in oculocutaneous albinism II (OCA2), a melanosome-specific transmembrane protein with unknown function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1248487.RA5x0tzdMooOhdQY8gVKSUGgpsT4zcjq9WEvxQssaYsGA130_provenance.
- NP1248487.RA5x0tzdMooOhdQY8gVKSUGgpsT4zcjq9WEvxQssaYsGA130_assertion evidence source_evidence_literature NP1248487.RA5x0tzdMooOhdQY8gVKSUGgpsT4zcjq9WEvxQssaYsGA130_provenance.
- NP1248487.RA5x0tzdMooOhdQY8gVKSUGgpsT4zcjq9WEvxQssaYsGA130_assertion SIO_000772 25513726 NP1248487.RA5x0tzdMooOhdQY8gVKSUGgpsT4zcjq9WEvxQssaYsGA130_provenance.
- NP1248487.RA5x0tzdMooOhdQY8gVKSUGgpsT4zcjq9WEvxQssaYsGA130_assertion wasDerivedFrom befree-2016 NP1248487.RA5x0tzdMooOhdQY8gVKSUGgpsT4zcjq9WEvxQssaYsGA130_provenance.
- NP1248487.RA5x0tzdMooOhdQY8gVKSUGgpsT4zcjq9WEvxQssaYsGA130_assertion wasGeneratedBy ECO_0000203 NP1248487.RA5x0tzdMooOhdQY8gVKSUGgpsT4zcjq9WEvxQssaYsGA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1248487.RA5x0tzdMooOhdQY8gVKSUGgpsT4zcjq9WEvxQssaYsGA130_provenance.