Source:http://linkedlifedata.com/resource/lhgdn/association:36371
| Subject | Predicate | Object | Context |
|---|---|---|---|
| lhgdn:association:36371 | lhgdn:found_in | pubmed-article:17634419 | lld:lhgdn |
| lhgdn:association:36371 | lhgdn:geneRifSource | Our results broaden the clinical spectrum associated with POMT2 mutations, which should be considered in patients with CMD associated with microcephaly, and severe mental retardation with or without ocular involvement. | lld:lhgdn |
| lhgdn:association:36371 | lhgdn:mesh_code | D008831 | lld:lhgdn |
| lhgdn:association:36371 | lhgdn:associationIdType | http://http://linkedlifedat... | lld:lhgdn |
| lhgdn:association:36371 | lhgdn:umls_code | umls-concept:C1956147 | lld:mappings |
| entrez-gene:29954 | lhgdn:associationId | lhgdn:association:36371 | lld:lhgdn |