Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP48893.RAdrhBdEN3Pl9jp_NAwKleCyN-S8-x8-IIQQIldF7z2Eg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP48893.RAdrhBdEN3Pl9jp_NAwKleCyN-S8-x8-IIQQIldF7z2Eg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP48893.RAdrhBdEN3Pl9jp_NAwKleCyN-S8-x8-IIQQIldF7z2Eg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP48893.RAdrhBdEN3Pl9jp_NAwKleCyN-S8-x8-IIQQIldF7z2Eg130_provenance.
- NP48893.RAdrhBdEN3Pl9jp_NAwKleCyN-S8-x8-IIQQIldF7z2Eg130_assertion description "[To investigate the role of haplotypes formed by these polymorphisms for angiotensinogen levels we examined blood pressure, coronary artery disease (CAD), myocardial infarction (MI), and AGT genotypes and haplotypes in 2,575 patients with angiographically documented CAD and 731 individuals in whom CAD had been ruled out by angiography.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48893.RAdrhBdEN3Pl9jp_NAwKleCyN-S8-x8-IIQQIldF7z2Eg130_provenance.
- NP48893.RAdrhBdEN3Pl9jp_NAwKleCyN-S8-x8-IIQQIldF7z2Eg130_assertion evidence source_evidence_literature NP48893.RAdrhBdEN3Pl9jp_NAwKleCyN-S8-x8-IIQQIldF7z2Eg130_provenance.
- NP48893.RAdrhBdEN3Pl9jp_NAwKleCyN-S8-x8-IIQQIldF7z2Eg130_assertion SIO_000772 15599691 NP48893.RAdrhBdEN3Pl9jp_NAwKleCyN-S8-x8-IIQQIldF7z2Eg130_provenance.
- NP48893.RAdrhBdEN3Pl9jp_NAwKleCyN-S8-x8-IIQQIldF7z2Eg130_assertion wasDerivedFrom gad-20130706 NP48893.RAdrhBdEN3Pl9jp_NAwKleCyN-S8-x8-IIQQIldF7z2Eg130_provenance.
- NP48893.RAdrhBdEN3Pl9jp_NAwKleCyN-S8-x8-IIQQIldF7z2Eg130_assertion wasGeneratedBy ECO_0000203 NP48893.RAdrhBdEN3Pl9jp_NAwKleCyN-S8-x8-IIQQIldF7z2Eg130_provenance.
- gad-20130706 importedOn "2013-07-06" NP48893.RAdrhBdEN3Pl9jp_NAwKleCyN-S8-x8-IIQQIldF7z2Eg130_provenance.