Source:http://linkedlifedata.com/resource/lhgdn/association:12379
| Subject | Predicate | Object | Context |
|---|---|---|---|
| lhgdn:association:12379 | lhgdn:found_in | pubmed-article:18434651 | lld:lhgdn |
| lhgdn:association:12379 | lhgdn:geneRifSource | homozygous mutations in DEHAL1 appear to cause human iodotyrosine deiodinase deficiency, leading to hereditary hypothyroidism and goiter | lld:lhgdn |
| lhgdn:association:12379 | lhgdn:mesh_code | D007037 | lld:lhgdn |
| lhgdn:association:12379 | lhgdn:associationIdType | http://http://linkedlifedat... | lld:lhgdn |
| lhgdn:association:12379 | lhgdn:umls_code | umls-concept:C0020676 | lld:mappings |
| entrez-gene:389434 | lhgdn:associationId | lhgdn:association:12379 | lld:lhgdn |