Source:http://linkedlifedata.com/resource/lhgdn/association:36133
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
high frequency of NRAS codon 61 mutations detected in primary hereditary melanomas may be the result of a hypermutability phenotype associated with a hereditary predisposition for melanoma development in patients with germline CDKN2A mutations
|
| lhgdn:mesh_code |
D008545
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |