Source:http://linkedlifedata.com/resource/lhgdn/association:2401
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
MSH2 c.1452-1455delAATG is a founder mutation and an important cause of hereditary nonpolyposis colorectal cancer in the southern Chinese population
|
| lhgdn:mesh_code |
D003123
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |