Source:http://linkedlifedata.com/resource/lhgdn/association:36133
| Subject | Predicate | Object | Context |
|---|---|---|---|
| lhgdn:association:36133 | lhgdn:found_in | pubmed-article:12783933 | lld:lhgdn |
| lhgdn:association:36133 | 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 | lld:lhgdn |
| lhgdn:association:36133 | lhgdn:mesh_code | D008545 | lld:lhgdn |
| lhgdn:association:36133 | lhgdn:associationIdType | http://http://linkedlifedat... | lld:lhgdn |
| lhgdn:association:36133 | lhgdn:umls_code | umls-concept:C0025202 | lld:mappings |
| entrez-gene:4893 | lhgdn:associationId | lhgdn:association:36133 | lld:lhgdn |