Source:http://linkedlifedata.com/resource/lhgdn/association:17042
| Subject | Predicate | Object | Context |
|---|---|---|---|
| lhgdn:association:17042 | lhgdn:found_in | pubmed-article:16086270 | lld:lhgdn |
| lhgdn:association:17042 | lhgdn:geneRifSource | Findings indicated that the 951-953 (delC) deletion mutation in the FOXL2 gene in the two patients resulted in truncated proteins and hence led to their blepharophimosis, ptosis, and epicanthus inversus syndrome. | lld:lhgdn |
| lhgdn:association:17042 | lhgdn:mesh_code | D016569 | lld:lhgdn |
| lhgdn:association:17042 | lhgdn:associationIdType | http://http://linkedlifedat... | lld:lhgdn |
| lhgdn:association:17042 | lhgdn:umls_code | umls-concept:C0005744 | lld:mappings |
| entrez-gene:668 | lhgdn:associationId | lhgdn:association:17042 | lld:lhgdn |