Source:http://linkedlifedata.com/resource/lhgdn/association:43420
| Subject | Predicate | Object | Context |
|---|---|---|---|
| lhgdn:association:43420 | lhgdn:found_in | pubmed-article:14676051 | lld:lhgdn |
| lhgdn:association:43420 | lhgdn:geneRifSource | Spinocerebellar ataxia (SCA) type 14 is caused by mutations in PRKCG gene/observation that all 4 PRKCG mutations identified in patients with SCA to date are located in exon 4 suggests a critical role for this region of the gene in cerebellar function. | lld:lhgdn |
| lhgdn:association:43420 | lhgdn:mesh_code | D020754 | lld:lhgdn |
| lhgdn:association:43420 | lhgdn:associationIdType | http://http://linkedlifedat... | lld:lhgdn |
| lhgdn:association:43420 | lhgdn:umls_code | umls-concept:C0752125 | lld:mappings |
| entrez-gene:5582 | lhgdn:associationId | lhgdn:association:43420 | lld:lhgdn |