Source:http://linkedlifedata.com/resource/lhgdn/association:30881
Predicate | Object |
---|---|
lhgdn:found_in | |
lhgdn:geneRifSource |
investigated whether the variant alleles CYP2C9*2 and CYP2C9*3 or the use of CYP2C9 substrates or inhibitors was associated with an increased risk of myocardial infarction
|
lhgdn:mesh_code |
D009203
|
lhgdn:associationIdType | |
lhgdn:umls_code |