Source:http://linkedlifedata.com/resource/lhgdn/association:47303
| Subject | Predicate | Object | Context |
|---|---|---|---|
| lhgdn:association:47303 | lhgdn:found_in | pubmed-article:17927801 | lld:lhgdn |
| lhgdn:association:47303 | lhgdn:geneRifSource | This suggests that mutations in the SCN1B gene is not a prevalent cause of familial cases of FS and epilepsy or GEFS+ in Scandinavia. | lld:lhgdn |
| lhgdn:association:47303 | lhgdn:mesh_code | D004827 | lld:lhgdn |
| lhgdn:association:47303 | lhgdn:associationIdType | http://bio2rdf.org/euadr:Ne... | lld:lhgdn |
| lhgdn:association:47303 | lhgdn:umls_code | umls-concept:C0236018 | lld:mappings |
| entrez-gene:6324 | lhgdn:associationId | lhgdn:association:47303 | lld:lhgdn |