Source:http://linkedlifedata.com/resource/lhgdn/association:10135
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
investigated whether the allelic variants 1019C and 1019T are differentially predictive of increased risk for coronary artery disease (CAD) and myocardial infarction (MI)
|
| lhgdn:mesh_code |
D009203
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |