Source:http://linkedlifedata.com/resource/lhgdn/association:50264
| Subject | Predicate | Object | Context |
|---|---|---|---|
| lhgdn:association:50264 | lhgdn:found_in | pubmed-article:16141009 | lld:lhgdn |
| lhgdn:association:50264 | lhgdn:geneRifSource | We thus expand the clinical spectrum of ASPM mutations by showing that they can occur in patients with seizures and that the history of seizures alone should not necessarily preclude the diagnosis of primary microcephaly. | lld:lhgdn |
| lhgdn:association:50264 | lhgdn:mesh_code | D008831 | lld:lhgdn |
| lhgdn:association:50264 | lhgdn:associationIdType | http://bio2rdf.org/euadr:Ne... | lld:lhgdn |
| lhgdn:association:50264 | lhgdn:umls_code | umls-concept:C1956147 | lld:mappings |
| entrez-gene:259266 | lhgdn:associationId | lhgdn:association:50264 | lld:lhgdn |