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- NP77656.RAmd4VBGR_I9Cj39QHQfn-1P0l5TeZfWWWPg87MzH09Ek130_assertion type Assertion NP77656.RAmd4VBGR_I9Cj39QHQfn-1P0l5TeZfWWWPg87MzH09Ek130_head.
- NP77656.RAmd4VBGR_I9Cj39QHQfn-1P0l5TeZfWWWPg87MzH09Ek130_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." NP77656.RAmd4VBGR_I9Cj39QHQfn-1P0l5TeZfWWWPg87MzH09Ek130_provenance.
- NP77656.RAmd4VBGR_I9Cj39QHQfn-1P0l5TeZfWWWPg87MzH09Ek130_assertion evidence source_evidence_literature NP77656.RAmd4VBGR_I9Cj39QHQfn-1P0l5TeZfWWWPg87MzH09Ek130_provenance.
- NP77656.RAmd4VBGR_I9Cj39QHQfn-1P0l5TeZfWWWPg87MzH09Ek130_assertion SIO_000772 20738937 NP77656.RAmd4VBGR_I9Cj39QHQfn-1P0l5TeZfWWWPg87MzH09Ek130_provenance.
- NP77656.RAmd4VBGR_I9Cj39QHQfn-1P0l5TeZfWWWPg87MzH09Ek130_assertion wasDerivedFrom gad-20130706 NP77656.RAmd4VBGR_I9Cj39QHQfn-1P0l5TeZfWWWPg87MzH09Ek130_provenance.
- NP77656.RAmd4VBGR_I9Cj39QHQfn-1P0l5TeZfWWWPg87MzH09Ek130_assertion wasGeneratedBy ECO_0000203 NP77656.RAmd4VBGR_I9Cj39QHQfn-1P0l5TeZfWWWPg87MzH09Ek130_provenance.