Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP184514.RA2AkMsuA2YaFqjCq9rGnk7cp5xh6sabqGjnHCZ2JfEiY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP184514.RA2AkMsuA2YaFqjCq9rGnk7cp5xh6sabqGjnHCZ2JfEiY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP184514.RA2AkMsuA2YaFqjCq9rGnk7cp5xh6sabqGjnHCZ2JfEiY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP184514.RA2AkMsuA2YaFqjCq9rGnk7cp5xh6sabqGjnHCZ2JfEiY130_provenance.
- NP184514.RA2AkMsuA2YaFqjCq9rGnk7cp5xh6sabqGjnHCZ2JfEiY130_assertion description "[A genetic risk score based on nine genetic variants independently associated with CAD irrespective of other cardiovascular risk factors was associated with the presence of the disease. Cohort studies are needed to determine whether this genetic risk score]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184514.RA2AkMsuA2YaFqjCq9rGnk7cp5xh6sabqGjnHCZ2JfEiY130_provenance.
- NP184514.RA2AkMsuA2YaFqjCq9rGnk7cp5xh6sabqGjnHCZ2JfEiY130_assertion evidence source_evidence_literature NP184514.RA2AkMsuA2YaFqjCq9rGnk7cp5xh6sabqGjnHCZ2JfEiY130_provenance.
- NP184514.RA2AkMsuA2YaFqjCq9rGnk7cp5xh6sabqGjnHCZ2JfEiY130_assertion SIO_000772 20738937 NP184514.RA2AkMsuA2YaFqjCq9rGnk7cp5xh6sabqGjnHCZ2JfEiY130_provenance.
- NP184514.RA2AkMsuA2YaFqjCq9rGnk7cp5xh6sabqGjnHCZ2JfEiY130_assertion wasDerivedFrom gad-20150221 NP184514.RA2AkMsuA2YaFqjCq9rGnk7cp5xh6sabqGjnHCZ2JfEiY130_provenance.
- NP184514.RA2AkMsuA2YaFqjCq9rGnk7cp5xh6sabqGjnHCZ2JfEiY130_assertion wasGeneratedBy ECO_0000203 NP184514.RA2AkMsuA2YaFqjCq9rGnk7cp5xh6sabqGjnHCZ2JfEiY130_provenance.
- gad-20150221 importedOn "2015-02-21" NP184514.RA2AkMsuA2YaFqjCq9rGnk7cp5xh6sabqGjnHCZ2JfEiY130_provenance.