Source:http://linkedlifedata.com/resource/lhgdn/association:47764
| Subject | Predicate | Object | Context |
|---|---|---|---|
| lhgdn:association:47764 | lhgdn:found_in | pubmed-article:17923635 | lld:lhgdn |
| lhgdn:association:47764 | lhgdn:geneRifSource | SCA2 is one of the genetic causes of Parkinson disease and multiple system atrophy | lld:lhgdn |
| lhgdn:association:47764 | lhgdn:mesh_code | D010300 | lld:lhgdn |
| lhgdn:association:47764 | lhgdn:associationIdType | http://bio2rdf.org/euadr:Po... | lld:lhgdn |
| lhgdn:association:47764 | lhgdn:umls_code | umls-concept:C0030567 | lld:mappings |
| entrez-gene:6311 | lhgdn:associationId | lhgdn:association:47764 | lld:lhgdn |