Source:http://linkedlifedata.com/resource/lhgdn/association:2473
Predicate | Object |
---|---|
lhgdn:found_in | |
lhgdn:geneRifSource |
Mutation in MSH2 is associated with hereditary nonpolyposis colorectal cancer syndrome
|
lhgdn:mesh_code |
D003123
|
lhgdn:associationIdType | |
lhgdn:umls_code |