Source:http://linkedlifedata.com/resource/lhgdn/association:36533
| Subject | Predicate | Object | Context |
|---|---|---|---|
| lhgdn:association:36533 | lhgdn:found_in | pubmed-article:19215732 | lld:lhgdn |
| lhgdn:association:36533 | lhgdn:geneRifSource | Primary microcephaly is an autosomal-recessive congenital disorder characterized by smaller brain size and mental retardation, in which homozygote mutations in STIL proteins are found. | lld:lhgdn |
| lhgdn:association:36533 | lhgdn:mesh_code | D008831 | lld:lhgdn |
| lhgdn:association:36533 | lhgdn:associationIdType | http://http://linkedlifedat... | lld:lhgdn |
| lhgdn:association:36533 | lhgdn:umls_code | umls-concept:C1956147 | lld:mappings |
| entrez-gene:6491 | lhgdn:associationId | lhgdn:association:36533 | lld:lhgdn |