Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP435005.RAVvPQmWT-f2mEvw3KrnUp3ENt8DS8MSshz9FG5iaOytU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP435005.RAVvPQmWT-f2mEvw3KrnUp3ENt8DS8MSshz9FG5iaOytU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP435005.RAVvPQmWT-f2mEvw3KrnUp3ENt8DS8MSshz9FG5iaOytU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP435005.RAVvPQmWT-f2mEvw3KrnUp3ENt8DS8MSshz9FG5iaOytU130_provenance.
- NP435005.RAVvPQmWT-f2mEvw3KrnUp3ENt8DS8MSshz9FG5iaOytU130_assertion description "[Persons homozygous for haplotype 3, which is a common variant of the glucocorticoid receptor gene, had a more than 2-fold increased risk of myocardial infarction (hazard ratio, 2.1; 95% confidence interval, 1.13-4.07) and an almost 3-fold increased risk of coronary heart disease (hazard ratio, 2.6; 95% confidence interval, 1.40-4.81) compared with nonhomozygous persons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP435005.RAVvPQmWT-f2mEvw3KrnUp3ENt8DS8MSshz9FG5iaOytU130_provenance.
- NP435005.RAVvPQmWT-f2mEvw3KrnUp3ENt8DS8MSshz9FG5iaOytU130_assertion evidence source_evidence_literature NP435005.RAVvPQmWT-f2mEvw3KrnUp3ENt8DS8MSshz9FG5iaOytU130_provenance.
- NP435005.RAVvPQmWT-f2mEvw3KrnUp3ENt8DS8MSshz9FG5iaOytU130_assertion SIO_000772 18195193 NP435005.RAVvPQmWT-f2mEvw3KrnUp3ENt8DS8MSshz9FG5iaOytU130_provenance.
- NP435005.RAVvPQmWT-f2mEvw3KrnUp3ENt8DS8MSshz9FG5iaOytU130_assertion wasDerivedFrom befree-20150227 NP435005.RAVvPQmWT-f2mEvw3KrnUp3ENt8DS8MSshz9FG5iaOytU130_provenance.
- NP435005.RAVvPQmWT-f2mEvw3KrnUp3ENt8DS8MSshz9FG5iaOytU130_assertion wasGeneratedBy ECO_0000203 NP435005.RAVvPQmWT-f2mEvw3KrnUp3ENt8DS8MSshz9FG5iaOytU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP435005.RAVvPQmWT-f2mEvw3KrnUp3ENt8DS8MSshz9FG5iaOytU130_provenance.