Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP130592.RAB2TCp9-BrI5x1gEq60uU5LA5TUv4orM2VI2sWWzgt_U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP130592.RAB2TCp9-BrI5x1gEq60uU5LA5TUv4orM2VI2sWWzgt_U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP130592.RAB2TCp9-BrI5x1gEq60uU5LA5TUv4orM2VI2sWWzgt_U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP130592.RAB2TCp9-BrI5x1gEq60uU5LA5TUv4orM2VI2sWWzgt_U130_provenance.
- NP130592.RAB2TCp9-BrI5x1gEq60uU5LA5TUv4orM2VI2sWWzgt_U130_assertion description "[Mutations in LRRK2 as a cause of Parkinson's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130592.RAB2TCp9-BrI5x1gEq60uU5LA5TUv4orM2VI2sWWzgt_U130_provenance.
- NP130592.RAB2TCp9-BrI5x1gEq60uU5LA5TUv4orM2VI2sWWzgt_U130_assertion evidence source_evidence_literature NP130592.RAB2TCp9-BrI5x1gEq60uU5LA5TUv4orM2VI2sWWzgt_U130_provenance.
- NP130592.RAB2TCp9-BrI5x1gEq60uU5LA5TUv4orM2VI2sWWzgt_U130_assertion SIO_000772 18097165 NP130592.RAB2TCp9-BrI5x1gEq60uU5LA5TUv4orM2VI2sWWzgt_U130_provenance.
- NP130592.RAB2TCp9-BrI5x1gEq60uU5LA5TUv4orM2VI2sWWzgt_U130_assertion wasDerivedFrom lhgdn-20090331 NP130592.RAB2TCp9-BrI5x1gEq60uU5LA5TUv4orM2VI2sWWzgt_U130_provenance.
- NP130592.RAB2TCp9-BrI5x1gEq60uU5LA5TUv4orM2VI2sWWzgt_U130_assertion wasGeneratedBy ECO_0000203 NP130592.RAB2TCp9-BrI5x1gEq60uU5LA5TUv4orM2VI2sWWzgt_U130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP130592.RAB2TCp9-BrI5x1gEq60uU5LA5TUv4orM2VI2sWWzgt_U130_provenance.