Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP116917.RAz2ktF1YLbRPRXems1fJ1eKpPPJR7e26Y_ngMXCd7f2g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP116917.RAz2ktF1YLbRPRXems1fJ1eKpPPJR7e26Y_ngMXCd7f2g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP116917.RAz2ktF1YLbRPRXems1fJ1eKpPPJR7e26Y_ngMXCd7f2g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP116917.RAz2ktF1YLbRPRXems1fJ1eKpPPJR7e26Y_ngMXCd7f2g130_provenance.
- NP116917.RAz2ktF1YLbRPRXems1fJ1eKpPPJR7e26Y_ngMXCd7f2g130_assertion description "[The findings support the association of several loci with AD, and suggest how intermediate phenotypes can enhance analysis of susceptibility loci in this complex genetic disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP116917.RAz2ktF1YLbRPRXems1fJ1eKpPPJR7e26Y_ngMXCd7f2g130_provenance.
- NP116917.RAz2ktF1YLbRPRXems1fJ1eKpPPJR7e26Y_ngMXCd7f2g130_assertion evidence source_evidence_literature NP116917.RAz2ktF1YLbRPRXems1fJ1eKpPPJR7e26Y_ngMXCd7f2g130_provenance.
- NP116917.RAz2ktF1YLbRPRXems1fJ1eKpPPJR7e26Y_ngMXCd7f2g130_assertion SIO_000772 20574532 NP116917.RAz2ktF1YLbRPRXems1fJ1eKpPPJR7e26Y_ngMXCd7f2g130_provenance.
- NP116917.RAz2ktF1YLbRPRXems1fJ1eKpPPJR7e26Y_ngMXCd7f2g130_assertion wasDerivedFrom gad-20150221 NP116917.RAz2ktF1YLbRPRXems1fJ1eKpPPJR7e26Y_ngMXCd7f2g130_provenance.
- NP116917.RAz2ktF1YLbRPRXems1fJ1eKpPPJR7e26Y_ngMXCd7f2g130_assertion wasGeneratedBy ECO_0000203 NP116917.RAz2ktF1YLbRPRXems1fJ1eKpPPJR7e26Y_ngMXCd7f2g130_provenance.
- gad-20150221 importedOn "2015-02-21" NP116917.RAz2ktF1YLbRPRXems1fJ1eKpPPJR7e26Y_ngMXCd7f2g130_provenance.