Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP269634.RAoQZW5Pyvej5fqQvU6bEhM8MK2bAvsTripiu6mtJ9VVI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP269634.RAoQZW5Pyvej5fqQvU6bEhM8MK2bAvsTripiu6mtJ9VVI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP269634.RAoQZW5Pyvej5fqQvU6bEhM8MK2bAvsTripiu6mtJ9VVI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP269634.RAoQZW5Pyvej5fqQvU6bEhM8MK2bAvsTripiu6mtJ9VVI130_provenance.
- NP269634.RAoQZW5Pyvej5fqQvU6bEhM8MK2bAvsTripiu6mtJ9VVI130_assertion description "[By stepwise logistic regression, in 261 women with ATCVD risk factor data, positive explanatory variables for ATCVD included the 20210 G/A prothrombin mutation (risk odds ratio, 5.8; 95% confidence intervals [CI], 1.4 to 30.2; P =.021) and a 20210 G/A prothrombin gene mutation*ERT interaction term (risk odds ratio, 2.70; 95% CI, 1.4 to 5.4; P =.004).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP269634.RAoQZW5Pyvej5fqQvU6bEhM8MK2bAvsTripiu6mtJ9VVI130_provenance.
- NP269634.RAoQZW5Pyvej5fqQvU6bEhM8MK2bAvsTripiu6mtJ9VVI130_assertion evidence source_evidence_literature NP269634.RAoQZW5Pyvej5fqQvU6bEhM8MK2bAvsTripiu6mtJ9VVI130_provenance.
- NP269634.RAoQZW5Pyvej5fqQvU6bEhM8MK2bAvsTripiu6mtJ9VVI130_assertion SIO_000772 11230792 NP269634.RAoQZW5Pyvej5fqQvU6bEhM8MK2bAvsTripiu6mtJ9VVI130_provenance.
- NP269634.RAoQZW5Pyvej5fqQvU6bEhM8MK2bAvsTripiu6mtJ9VVI130_assertion wasDerivedFrom befree-20140225 NP269634.RAoQZW5Pyvej5fqQvU6bEhM8MK2bAvsTripiu6mtJ9VVI130_provenance.
- NP269634.RAoQZW5Pyvej5fqQvU6bEhM8MK2bAvsTripiu6mtJ9VVI130_assertion wasGeneratedBy ECO_0000203 NP269634.RAoQZW5Pyvej5fqQvU6bEhM8MK2bAvsTripiu6mtJ9VVI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP269634.RAoQZW5Pyvej5fqQvU6bEhM8MK2bAvsTripiu6mtJ9VVI130_provenance.