Source:http://linkedlifedata.com/resource/lhgdn/association:23300
| Subject | Predicate | Object | Context |
|---|---|---|---|
| lhgdn:association:23300 | lhgdn:found_in | pubmed-article:16966502 | lld:lhgdn |
| lhgdn:association:23300 | lhgdn:geneRifSource | Parkinson disease related to LRRK2 is characterized by typical clinical features, and the similarities between patients with homozygous and heterozygous mutations do not support a gene dosage effect. | lld:lhgdn |
| lhgdn:association:23300 | lhgdn:mesh_code | D010300 | lld:lhgdn |
| lhgdn:association:23300 | lhgdn:associationIdType | http://http://linkedlifedat... | lld:lhgdn |
| lhgdn:association:23300 | lhgdn:umls_code | umls-concept:C0030567 | lld:mappings |
| entrez-gene:120892 | lhgdn:associationId | lhgdn:association:23300 | lld:lhgdn |