Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP91167.RAhJxAgI6doVnLDrBJQhCqi8Q6g_uPbNOJRVu5qqe7luo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP91167.RAhJxAgI6doVnLDrBJQhCqi8Q6g_uPbNOJRVu5qqe7luo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP91167.RAhJxAgI6doVnLDrBJQhCqi8Q6g_uPbNOJRVu5qqe7luo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP91167.RAhJxAgI6doVnLDrBJQhCqi8Q6g_uPbNOJRVu5qqe7luo130_provenance.
- NP91167.RAhJxAgI6doVnLDrBJQhCqi8Q6g_uPbNOJRVu5qqe7luo130_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 can improve the predictive capacity or the risk classification of classical risk functions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP91167.RAhJxAgI6doVnLDrBJQhCqi8Q6g_uPbNOJRVu5qqe7luo130_provenance.
- NP91167.RAhJxAgI6doVnLDrBJQhCqi8Q6g_uPbNOJRVu5qqe7luo130_assertion evidence source_evidence_literature NP91167.RAhJxAgI6doVnLDrBJQhCqi8Q6g_uPbNOJRVu5qqe7luo130_provenance.
- NP91167.RAhJxAgI6doVnLDrBJQhCqi8Q6g_uPbNOJRVu5qqe7luo130_assertion SIO_000772 20738937 NP91167.RAhJxAgI6doVnLDrBJQhCqi8Q6g_uPbNOJRVu5qqe7luo130_provenance.
- NP91167.RAhJxAgI6doVnLDrBJQhCqi8Q6g_uPbNOJRVu5qqe7luo130_assertion wasDerivedFrom gad-20130706 NP91167.RAhJxAgI6doVnLDrBJQhCqi8Q6g_uPbNOJRVu5qqe7luo130_provenance.
- NP91167.RAhJxAgI6doVnLDrBJQhCqi8Q6g_uPbNOJRVu5qqe7luo130_assertion wasGeneratedBy ECO_0000203 NP91167.RAhJxAgI6doVnLDrBJQhCqi8Q6g_uPbNOJRVu5qqe7luo130_provenance.
- gad-20130706 importedOn "2013-07-06" NP91167.RAhJxAgI6doVnLDrBJQhCqi8Q6g_uPbNOJRVu5qqe7luo130_provenance.