Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP60792.RAEtAWjnfGTprrkfA2O4ibe8682Rl14mXF47Eoab8LNDk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP60792.RAEtAWjnfGTprrkfA2O4ibe8682Rl14mXF47Eoab8LNDk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP60792.RAEtAWjnfGTprrkfA2O4ibe8682Rl14mXF47Eoab8LNDk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP60792.RAEtAWjnfGTprrkfA2O4ibe8682Rl14mXF47Eoab8LNDk130_provenance.
- NP60792.RAEtAWjnfGTprrkfA2O4ibe8682Rl14mXF47Eoab8LNDk130_assertion description "[We performed a meta-analysis of 53 studies comprising 17,791 subjects investigating the angiotensin-I converting enzyme insertion/deletion polymorphism, taking into account the requirement for diabetic retinopathy in the case definition and assuming a random-effects model.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP60792.RAEtAWjnfGTprrkfA2O4ibe8682Rl14mXF47Eoab8LNDk130_provenance.
- NP60792.RAEtAWjnfGTprrkfA2O4ibe8682Rl14mXF47Eoab8LNDk130_assertion evidence source_evidence_literature NP60792.RAEtAWjnfGTprrkfA2O4ibe8682Rl14mXF47Eoab8LNDk130_provenance.
- NP60792.RAEtAWjnfGTprrkfA2O4ibe8682Rl14mXF47Eoab8LNDk130_assertion SIO_000772 18523141 NP60792.RAEtAWjnfGTprrkfA2O4ibe8682Rl14mXF47Eoab8LNDk130_provenance.
- NP60792.RAEtAWjnfGTprrkfA2O4ibe8682Rl14mXF47Eoab8LNDk130_assertion wasDerivedFrom gad-20150221 NP60792.RAEtAWjnfGTprrkfA2O4ibe8682Rl14mXF47Eoab8LNDk130_provenance.
- NP60792.RAEtAWjnfGTprrkfA2O4ibe8682Rl14mXF47Eoab8LNDk130_assertion wasGeneratedBy ECO_0000203 NP60792.RAEtAWjnfGTprrkfA2O4ibe8682Rl14mXF47Eoab8LNDk130_provenance.
- gad-20150221 importedOn "2015-02-21" NP60792.RAEtAWjnfGTprrkfA2O4ibe8682Rl14mXF47Eoab8LNDk130_provenance.