Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP440716.RAYQuOPTmKktVw6WpQKYogM18QzdBq7VW1z8ktvflr2nU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP440716.RAYQuOPTmKktVw6WpQKYogM18QzdBq7VW1z8ktvflr2nU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP440716.RAYQuOPTmKktVw6WpQKYogM18QzdBq7VW1z8ktvflr2nU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP440716.RAYQuOPTmKktVw6WpQKYogM18QzdBq7VW1z8ktvflr2nU130_provenance.
- NP440716.RAYQuOPTmKktVw6WpQKYogM18QzdBq7VW1z8ktvflr2nU130_assertion description "[Copy number variations in regulators of complement activation genes (CFHR1 and CFHR3) and glutathione S transferase genes (GSTM1 and GSTT1) have been associated with AMD, and several additional loci have been identified as regions of potential interest but require further evaluation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP440716.RAYQuOPTmKktVw6WpQKYogM18QzdBq7VW1z8ktvflr2nU130_provenance.
- NP440716.RAYQuOPTmKktVw6WpQKYogM18QzdBq7VW1z8ktvflr2nU130_assertion evidence source_evidence_literature NP440716.RAYQuOPTmKktVw6WpQKYogM18QzdBq7VW1z8ktvflr2nU130_provenance.
- NP440716.RAYQuOPTmKktVw6WpQKYogM18QzdBq7VW1z8ktvflr2nU130_assertion SIO_000772 23244519 NP440716.RAYQuOPTmKktVw6WpQKYogM18QzdBq7VW1z8ktvflr2nU130_provenance.
- NP440716.RAYQuOPTmKktVw6WpQKYogM18QzdBq7VW1z8ktvflr2nU130_assertion wasDerivedFrom befree-20150227 NP440716.RAYQuOPTmKktVw6WpQKYogM18QzdBq7VW1z8ktvflr2nU130_provenance.
- NP440716.RAYQuOPTmKktVw6WpQKYogM18QzdBq7VW1z8ktvflr2nU130_assertion wasGeneratedBy ECO_0000203 NP440716.RAYQuOPTmKktVw6WpQKYogM18QzdBq7VW1z8ktvflr2nU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP440716.RAYQuOPTmKktVw6WpQKYogM18QzdBq7VW1z8ktvflr2nU130_provenance.