Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP373187.RAoPlZhjuQWCQEtKF7e8iP0D6CHccHr8ei3ryIss7RN0E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP373187.RAoPlZhjuQWCQEtKF7e8iP0D6CHccHr8ei3ryIss7RN0E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP373187.RAoPlZhjuQWCQEtKF7e8iP0D6CHccHr8ei3ryIss7RN0E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP373187.RAoPlZhjuQWCQEtKF7e8iP0D6CHccHr8ei3ryIss7RN0E130_provenance.
- NP373187.RAoPlZhjuQWCQEtKF7e8iP0D6CHccHr8ei3ryIss7RN0E130_assertion description "[We suggest that the 20210 G/A prothrombin gene mutation be measured in all women on ERT or before beginning ERT to identify those heterozygous for the thrombophilic prothrombin gene mutation (4%) in whom ERT is contraindicated because of increased risk for ATCVD and thromboembolism, and a second, much larger group of women without the 20210 G/A prothrombin gene mutation (96%) in whom ERT may possibly reduce risk for ATCVD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP373187.RAoPlZhjuQWCQEtKF7e8iP0D6CHccHr8ei3ryIss7RN0E130_provenance.
- NP373187.RAoPlZhjuQWCQEtKF7e8iP0D6CHccHr8ei3ryIss7RN0E130_assertion evidence source_evidence_literature NP373187.RAoPlZhjuQWCQEtKF7e8iP0D6CHccHr8ei3ryIss7RN0E130_provenance.
- NP373187.RAoPlZhjuQWCQEtKF7e8iP0D6CHccHr8ei3ryIss7RN0E130_assertion SIO_000772 11230792 NP373187.RAoPlZhjuQWCQEtKF7e8iP0D6CHccHr8ei3ryIss7RN0E130_provenance.
- NP373187.RAoPlZhjuQWCQEtKF7e8iP0D6CHccHr8ei3ryIss7RN0E130_assertion wasDerivedFrom befree-20150227 NP373187.RAoPlZhjuQWCQEtKF7e8iP0D6CHccHr8ei3ryIss7RN0E130_provenance.
- NP373187.RAoPlZhjuQWCQEtKF7e8iP0D6CHccHr8ei3ryIss7RN0E130_assertion wasGeneratedBy ECO_0000203 NP373187.RAoPlZhjuQWCQEtKF7e8iP0D6CHccHr8ei3ryIss7RN0E130_provenance.
- befree-20150227 importedOn "2015-02-27" NP373187.RAoPlZhjuQWCQEtKF7e8iP0D6CHccHr8ei3ryIss7RN0E130_provenance.