Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP511820.RAmiNvuMa3_H-3xJ4YC-cRyx9w9OeLOkM9sxORkrH25lE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP511820.RAmiNvuMa3_H-3xJ4YC-cRyx9w9OeLOkM9sxORkrH25lE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP511820.RAmiNvuMa3_H-3xJ4YC-cRyx9w9OeLOkM9sxORkrH25lE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP511820.RAmiNvuMa3_H-3xJ4YC-cRyx9w9OeLOkM9sxORkrH25lE130_provenance.
- NP511820.RAmiNvuMa3_H-3xJ4YC-cRyx9w9OeLOkM9sxORkrH25lE130_assertion description "[Gene polymorphism of the renin-angiotensin system associates with risk for lacunar infarction. The Ohasama study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP511820.RAmiNvuMa3_H-3xJ4YC-cRyx9w9OeLOkM9sxORkrH25lE130_provenance.
- NP511820.RAmiNvuMa3_H-3xJ4YC-cRyx9w9OeLOkM9sxORkrH25lE130_assertion evidence source_evidence_literature NP511820.RAmiNvuMa3_H-3xJ4YC-cRyx9w9OeLOkM9sxORkrH25lE130_provenance.
- NP511820.RAmiNvuMa3_H-3xJ4YC-cRyx9w9OeLOkM9sxORkrH25lE130_assertion SIO_000772 10701810 NP511820.RAmiNvuMa3_H-3xJ4YC-cRyx9w9OeLOkM9sxORkrH25lE130_provenance.
- NP511820.RAmiNvuMa3_H-3xJ4YC-cRyx9w9OeLOkM9sxORkrH25lE130_assertion wasDerivedFrom befree-20140225 NP511820.RAmiNvuMa3_H-3xJ4YC-cRyx9w9OeLOkM9sxORkrH25lE130_provenance.
- NP511820.RAmiNvuMa3_H-3xJ4YC-cRyx9w9OeLOkM9sxORkrH25lE130_assertion wasGeneratedBy ECO_0000203 NP511820.RAmiNvuMa3_H-3xJ4YC-cRyx9w9OeLOkM9sxORkrH25lE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP511820.RAmiNvuMa3_H-3xJ4YC-cRyx9w9OeLOkM9sxORkrH25lE130_provenance.