Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP76865.RApvbDzb95zCz7uOEVsIgvRqbUUkimTSgFvxiLd_eCMvE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP76865.RApvbDzb95zCz7uOEVsIgvRqbUUkimTSgFvxiLd_eCMvE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP76865.RApvbDzb95zCz7uOEVsIgvRqbUUkimTSgFvxiLd_eCMvE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP76865.RApvbDzb95zCz7uOEVsIgvRqbUUkimTSgFvxiLd_eCMvE130_provenance.
- NP76865.RApvbDzb95zCz7uOEVsIgvRqbUUkimTSgFvxiLd_eCMvE130_assertion description "[APOE is a risk gene for amnestic MCI and that ACT and CHRNA7 may act in these patients as modifier genes for the time of progression to AD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP76865.RApvbDzb95zCz7uOEVsIgvRqbUUkimTSgFvxiLd_eCMvE130_provenance.
- NP76865.RApvbDzb95zCz7uOEVsIgvRqbUUkimTSgFvxiLd_eCMvE130_assertion evidence source_evidence_literature NP76865.RApvbDzb95zCz7uOEVsIgvRqbUUkimTSgFvxiLd_eCMvE130_provenance.
- NP76865.RApvbDzb95zCz7uOEVsIgvRqbUUkimTSgFvxiLd_eCMvE130_assertion SIO_000772 18078695 NP76865.RApvbDzb95zCz7uOEVsIgvRqbUUkimTSgFvxiLd_eCMvE130_provenance.
- NP76865.RApvbDzb95zCz7uOEVsIgvRqbUUkimTSgFvxiLd_eCMvE130_assertion wasDerivedFrom gad-20150221 NP76865.RApvbDzb95zCz7uOEVsIgvRqbUUkimTSgFvxiLd_eCMvE130_provenance.
- NP76865.RApvbDzb95zCz7uOEVsIgvRqbUUkimTSgFvxiLd_eCMvE130_assertion wasGeneratedBy ECO_0000203 NP76865.RApvbDzb95zCz7uOEVsIgvRqbUUkimTSgFvxiLd_eCMvE130_provenance.
- gad-20150221 importedOn "2015-02-21" NP76865.RApvbDzb95zCz7uOEVsIgvRqbUUkimTSgFvxiLd_eCMvE130_provenance.