Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP87985.RAhzKPHwnLWvr0elHyN7Ef7whRDpT39f579qg1gkCTdOA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP87985.RAhzKPHwnLWvr0elHyN7Ef7whRDpT39f579qg1gkCTdOA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP87985.RAhzKPHwnLWvr0elHyN7Ef7whRDpT39f579qg1gkCTdOA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP87985.RAhzKPHwnLWvr0elHyN7Ef7whRDpT39f579qg1gkCTdOA130_provenance.
- NP87985.RAhzKPHwnLWvr0elHyN7Ef7whRDpT39f579qg1gkCTdOA130_assertion description "[The Intermountain Healthcares Coronary Genetics study demonstrates the ability of a multigenic, multipathway GRS to improve discrimination of angiographic CAD. Genetic risk scores promise to increase understanding of the genetic basis of CAD and improve identification of individuals at increased CAD risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87985.RAhzKPHwnLWvr0elHyN7Ef7whRDpT39f579qg1gkCTdOA130_provenance.
- NP87985.RAhzKPHwnLWvr0elHyN7Ef7whRDpT39f579qg1gkCTdOA130_assertion evidence source_evidence_literature NP87985.RAhzKPHwnLWvr0elHyN7Ef7whRDpT39f579qg1gkCTdOA130_provenance.
- NP87985.RAhzKPHwnLWvr0elHyN7Ef7whRDpT39f579qg1gkCTdOA130_assertion SIO_000772 20691829 NP87985.RAhzKPHwnLWvr0elHyN7Ef7whRDpT39f579qg1gkCTdOA130_provenance.
- NP87985.RAhzKPHwnLWvr0elHyN7Ef7whRDpT39f579qg1gkCTdOA130_assertion wasDerivedFrom gad-20130706 NP87985.RAhzKPHwnLWvr0elHyN7Ef7whRDpT39f579qg1gkCTdOA130_provenance.
- NP87985.RAhzKPHwnLWvr0elHyN7Ef7whRDpT39f579qg1gkCTdOA130_assertion wasGeneratedBy ECO_0000203 NP87985.RAhzKPHwnLWvr0elHyN7Ef7whRDpT39f579qg1gkCTdOA130_provenance.
- gad-20130706 importedOn "2013-07-06" NP87985.RAhzKPHwnLWvr0elHyN7Ef7whRDpT39f579qg1gkCTdOA130_provenance.