Source:http://linkedlifedata.com/resource/lhgdn/association:39161
| Subject | Predicate | Object | Context |
|---|---|---|---|
| lhgdn:association:39161 | lhgdn:found_in | pubmed-article:16314483 | lld:lhgdn |
| lhgdn:association:39161 | lhgdn:geneRifSource | Homozygosity at codon 129 suggests that codon 129 coupled with the mutation as well as that located on the normal allele can modify major phenotypic features of Creutzfeldt Jakob disease. | lld:lhgdn |
| lhgdn:association:39161 | lhgdn:mesh_code | D007562 | lld:lhgdn |
| lhgdn:association:39161 | lhgdn:associationIdType | http://http://linkedlifedat... | lld:lhgdn |
| lhgdn:association:39161 | lhgdn:umls_code | umls-concept:C0751254 | lld:mappings |
| entrez-gene:5621 | lhgdn:associationId | lhgdn:association:39161 | lld:lhgdn |