Source:http://linkedlifedata.com/resource/lhgdn/association:2637
Subject | Predicate | Object | Context |
---|---|---|---|
lhgdn:association:2637 | lhgdn:found_in | pubmed-article:18513969 | lld:lhgdn |
lhgdn:association:2637 | lhgdn:geneRifSource | Thirteen CMD patients showed mutations in POMT1, But normal brain MRI associated with mental retardation and microcephaly.mutations in POMT1 (six out of 13). | lld:lhgdn |
lhgdn:association:2637 | lhgdn:mesh_code | D008831 | lld:lhgdn |
lhgdn:association:2637 | lhgdn:associationIdType | http://http://linkedlifedat... | lld:lhgdn |
lhgdn:association:2637 | lhgdn:umls_code | umls-concept:C1956147 | lld:mappings |
entrez-gene:10585 | lhgdn:associationId | lhgdn:association:2637 | lld:lhgdn |