Source:http://linkedlifedata.com/resource/lhgdn/association:62698
| Subject | Predicate | Object | Context |
|---|---|---|---|
| lhgdn:association:62698 | lhgdn:found_in | pubmed-article:12244316 | lld:lhgdn |
| lhgdn:association:62698 | lhgdn:geneRifSource | loss-of-function mutations in TDP1 may cause spinocerebellar ataxia with axonal neuropathy either by interfering with DNA transcription or by inducing apoptosis in postmitotic neurons | lld:lhgdn |
| lhgdn:association:62698 | lhgdn:mesh_code | D020754 | lld:lhgdn |
| lhgdn:association:62698 | lhgdn:associationIdType | http://http://linkedlifedat... | lld:lhgdn |
| lhgdn:association:62698 | lhgdn:umls_code | umls-concept:C0752125 | lld:mappings |
| entrez-gene:55775 | lhgdn:associationId | lhgdn:association:62698 | lld:lhgdn |