Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP919085.RAVEsnf59U4OsdggldtO6O04HszH6pUejYe9b4lFSSDPQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP919085.RAVEsnf59U4OsdggldtO6O04HszH6pUejYe9b4lFSSDPQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP919085.RAVEsnf59U4OsdggldtO6O04HszH6pUejYe9b4lFSSDPQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP919085.RAVEsnf59U4OsdggldtO6O04HszH6pUejYe9b4lFSSDPQ130_provenance.
- NP919085.RAVEsnf59U4OsdggldtO6O04HszH6pUejYe9b4lFSSDPQ130_assertion description "[The present study indicates that the NPY T1128C polymorphism is an independent predictor for myocardial infarction and stroke in a Swedish hypertensive population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP919085.RAVEsnf59U4OsdggldtO6O04HszH6pUejYe9b4lFSSDPQ130_provenance.
- NP919085.RAVEsnf59U4OsdggldtO6O04HszH6pUejYe9b4lFSSDPQ130_assertion evidence source_evidence_literature NP919085.RAVEsnf59U4OsdggldtO6O04HszH6pUejYe9b4lFSSDPQ130_provenance.
- NP919085.RAVEsnf59U4OsdggldtO6O04HszH6pUejYe9b4lFSSDPQ130_assertion SIO_000772 15201542 NP919085.RAVEsnf59U4OsdggldtO6O04HszH6pUejYe9b4lFSSDPQ130_provenance.
- NP919085.RAVEsnf59U4OsdggldtO6O04HszH6pUejYe9b4lFSSDPQ130_assertion wasDerivedFrom befree-20140225 NP919085.RAVEsnf59U4OsdggldtO6O04HszH6pUejYe9b4lFSSDPQ130_provenance.
- NP919085.RAVEsnf59U4OsdggldtO6O04HszH6pUejYe9b4lFSSDPQ130_assertion wasGeneratedBy ECO_0000203 NP919085.RAVEsnf59U4OsdggldtO6O04HszH6pUejYe9b4lFSSDPQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP919085.RAVEsnf59U4OsdggldtO6O04HszH6pUejYe9b4lFSSDPQ130_provenance.