Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP615122.RAJS9s2RIagGz-llZkcH1pOMb1ES0jHE5K1EaPB_0MP-8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP615122.RAJS9s2RIagGz-llZkcH1pOMb1ES0jHE5K1EaPB_0MP-8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP615122.RAJS9s2RIagGz-llZkcH1pOMb1ES0jHE5K1EaPB_0MP-8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP615122.RAJS9s2RIagGz-llZkcH1pOMb1ES0jHE5K1EaPB_0MP-8130_provenance.
- NP615122.RAJS9s2RIagGz-llZkcH1pOMb1ES0jHE5K1EaPB_0MP-8130_assertion description "[We tested the impact of genetic risk score (GRS(24SNP/CAD)) calculated as a weighted (by allelic odds ratios for CAD) sum of CAD risk alleles from the studied 24 variants on CIMT, CAE, the incidence of carotid atherosclerosis and the progression of CIMT and CAE during a 6-year follow-up.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP615122.RAJS9s2RIagGz-llZkcH1pOMb1ES0jHE5K1EaPB_0MP-8130_provenance.
- NP615122.RAJS9s2RIagGz-llZkcH1pOMb1ES0jHE5K1EaPB_0MP-8130_assertion evidence source_evidence_literature NP615122.RAJS9s2RIagGz-llZkcH1pOMb1ES0jHE5K1EaPB_0MP-8130_provenance.
- NP615122.RAJS9s2RIagGz-llZkcH1pOMb1ES0jHE5K1EaPB_0MP-8130_assertion SIO_000772 22295058 NP615122.RAJS9s2RIagGz-llZkcH1pOMb1ES0jHE5K1EaPB_0MP-8130_provenance.
- NP615122.RAJS9s2RIagGz-llZkcH1pOMb1ES0jHE5K1EaPB_0MP-8130_assertion wasDerivedFrom befree-20140225 NP615122.RAJS9s2RIagGz-llZkcH1pOMb1ES0jHE5K1EaPB_0MP-8130_provenance.
- NP615122.RAJS9s2RIagGz-llZkcH1pOMb1ES0jHE5K1EaPB_0MP-8130_assertion wasGeneratedBy ECO_0000203 NP615122.RAJS9s2RIagGz-llZkcH1pOMb1ES0jHE5K1EaPB_0MP-8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP615122.RAJS9s2RIagGz-llZkcH1pOMb1ES0jHE5K1EaPB_0MP-8130_provenance.