Source:http://linkedlifedata.com/resource/lhgdn/association:38358
| Subject | Predicate | Object | Context |
|---|---|---|---|
| lhgdn:association:38358 | lhgdn:found_in | pubmed-article:18579156 | lld:lhgdn |
| lhgdn:association:38358 | lhgdn:geneRifSource | novel Thr49Pro TTR gene mutation is associated with leptomeningeal amyloidosis resulting in recurrent CNS symptoms | lld:lhgdn |
| lhgdn:association:38358 | lhgdn:mesh_code | D000686 | lld:lhgdn |
| lhgdn:association:38358 | lhgdn:associationIdType | http://http://linkedlifedat... | lld:lhgdn |
| lhgdn:association:38358 | lhgdn:umls_code | umls-concept:C0002726 | lld:mappings |
| entrez-gene:7276 | lhgdn:associationId | lhgdn:association:38358 | lld:lhgdn |