Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP222959.RAo2sZCLEjkjqREYE_86hF-H1zRRyolzGyRj_180VY9b0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP222959.RAo2sZCLEjkjqREYE_86hF-H1zRRyolzGyRj_180VY9b0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP222959.RAo2sZCLEjkjqREYE_86hF-H1zRRyolzGyRj_180VY9b0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP222959.RAo2sZCLEjkjqREYE_86hF-H1zRRyolzGyRj_180VY9b0130_provenance.
- NP222959.RAo2sZCLEjkjqREYE_86hF-H1zRRyolzGyRj_180VY9b0130_assertion description "[In a case-control sample that has shown the well established associations between AMD and variants in CFH, CFB and C3 there was absence of association with SNPs in CFP, CD46, CD55 and CD59.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP222959.RAo2sZCLEjkjqREYE_86hF-H1zRRyolzGyRj_180VY9b0130_provenance.
- NP222959.RAo2sZCLEjkjqREYE_86hF-H1zRRyolzGyRj_180VY9b0130_assertion evidence source_evidence_literature NP222959.RAo2sZCLEjkjqREYE_86hF-H1zRRyolzGyRj_180VY9b0130_provenance.
- NP222959.RAo2sZCLEjkjqREYE_86hF-H1zRRyolzGyRj_180VY9b0130_assertion SIO_000772 22024702 NP222959.RAo2sZCLEjkjqREYE_86hF-H1zRRyolzGyRj_180VY9b0130_provenance.
- NP222959.RAo2sZCLEjkjqREYE_86hF-H1zRRyolzGyRj_180VY9b0130_assertion wasDerivedFrom befree-20140225 NP222959.RAo2sZCLEjkjqREYE_86hF-H1zRRyolzGyRj_180VY9b0130_provenance.
- NP222959.RAo2sZCLEjkjqREYE_86hF-H1zRRyolzGyRj_180VY9b0130_assertion wasGeneratedBy ECO_0000203 NP222959.RAo2sZCLEjkjqREYE_86hF-H1zRRyolzGyRj_180VY9b0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP222959.RAo2sZCLEjkjqREYE_86hF-H1zRRyolzGyRj_180VY9b0130_provenance.