Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP52800.RA5o4yiU6fs05p27i633DwDQ2qR1MDCrQIeLPcd-hS7T0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP52800.RA5o4yiU6fs05p27i633DwDQ2qR1MDCrQIeLPcd-hS7T0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP52800.RA5o4yiU6fs05p27i633DwDQ2qR1MDCrQIeLPcd-hS7T0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP52800.RA5o4yiU6fs05p27i633DwDQ2qR1MDCrQIeLPcd-hS7T0130_provenance.
- NP52800.RA5o4yiU6fs05p27i633DwDQ2qR1MDCrQIeLPcd-hS7T0130_assertion description "[These findings suggest that the 20210A prothrombin allele represents an inherited risk factor for acute coronary syndrome among patients who have limited extent of coronary disease at angiography or who lack major metabolic and acquired risk factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52800.RA5o4yiU6fs05p27i633DwDQ2qR1MDCrQIeLPcd-hS7T0130_provenance.
- NP52800.RA5o4yiU6fs05p27i633DwDQ2qR1MDCrQIeLPcd-hS7T0130_assertion evidence source_evidence_literature NP52800.RA5o4yiU6fs05p27i633DwDQ2qR1MDCrQIeLPcd-hS7T0130_provenance.
- NP52800.RA5o4yiU6fs05p27i633DwDQ2qR1MDCrQIeLPcd-hS7T0130_assertion SIO_000772 11741359 NP52800.RA5o4yiU6fs05p27i633DwDQ2qR1MDCrQIeLPcd-hS7T0130_provenance.
- NP52800.RA5o4yiU6fs05p27i633DwDQ2qR1MDCrQIeLPcd-hS7T0130_assertion wasDerivedFrom gad-20150221 NP52800.RA5o4yiU6fs05p27i633DwDQ2qR1MDCrQIeLPcd-hS7T0130_provenance.
- NP52800.RA5o4yiU6fs05p27i633DwDQ2qR1MDCrQIeLPcd-hS7T0130_assertion wasGeneratedBy ECO_0000203 NP52800.RA5o4yiU6fs05p27i633DwDQ2qR1MDCrQIeLPcd-hS7T0130_provenance.
- gad-20150221 importedOn "2015-02-21" NP52800.RA5o4yiU6fs05p27i633DwDQ2qR1MDCrQIeLPcd-hS7T0130_provenance.