Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP193787.RAZ-NSh6aHhlPLjmdeKtRMwZ3DUHzGGBgND8pabnmmuCg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP193787.RAZ-NSh6aHhlPLjmdeKtRMwZ3DUHzGGBgND8pabnmmuCg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP193787.RAZ-NSh6aHhlPLjmdeKtRMwZ3DUHzGGBgND8pabnmmuCg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP193787.RAZ-NSh6aHhlPLjmdeKtRMwZ3DUHzGGBgND8pabnmmuCg130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP193787.RAZ-NSh6aHhlPLjmdeKtRMwZ3DUHzGGBgND8pabnmmuCg130_provenance.
- NP193787.RAZ-NSh6aHhlPLjmdeKtRMwZ3DUHzGGBgND8pabnmmuCg130_assertion wasGeneratedBy ECO_0000203 NP193787.RAZ-NSh6aHhlPLjmdeKtRMwZ3DUHzGGBgND8pabnmmuCg130_provenance.
- NP193787.RAZ-NSh6aHhlPLjmdeKtRMwZ3DUHzGGBgND8pabnmmuCg130_assertion wasDerivedFrom lhgdn-20090331 NP193787.RAZ-NSh6aHhlPLjmdeKtRMwZ3DUHzGGBgND8pabnmmuCg130_provenance.
- NP193787.RAZ-NSh6aHhlPLjmdeKtRMwZ3DUHzGGBgND8pabnmmuCg130_assertion SIO_000772 16358335 NP193787.RAZ-NSh6aHhlPLjmdeKtRMwZ3DUHzGGBgND8pabnmmuCg130_provenance.
- NP193787.RAZ-NSh6aHhlPLjmdeKtRMwZ3DUHzGGBgND8pabnmmuCg130_assertion evidence source_evidence_literature NP193787.RAZ-NSh6aHhlPLjmdeKtRMwZ3DUHzGGBgND8pabnmmuCg130_provenance.
- NP193787.RAZ-NSh6aHhlPLjmdeKtRMwZ3DUHzGGBgND8pabnmmuCg130_assertion description "[Two families with SNCA duplication were identified among autosomal dominant hereditary Parkinson's disease patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP193787.RAZ-NSh6aHhlPLjmdeKtRMwZ3DUHzGGBgND8pabnmmuCg130_provenance.