Source:http://linkedlifedata.com/resource/lhgdn/association:2432
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
The founder mutation MSH2*1906G-- > C is an important cause of hereditary nonpolyposis colorectal cancer in the Ashkenazi Jewish population
|
| lhgdn:mesh_code |
D003123
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |