Source:http://linkedlifedata.com/resource/lhgdn/association:29782
Subject | Predicate | Object | Context |
---|---|---|---|
lhgdn:association:29782 | lhgdn:found_in | pubmed-article:16390615 | lld:lhgdn |
lhgdn:association:29782 | lhgdn:geneRifSource | Sequencing of the hydroxymethylbilane synthase and uroporphyrinogen decarboxylase genes confirmed the relatively rare diagnosis of dual porphyria, and revealed a novel uroporphyrinogen decarboxylase mutation | lld:lhgdn |
lhgdn:association:29782 | lhgdn:mesh_code | D011164 | lld:lhgdn |
lhgdn:association:29782 | lhgdn:associationIdType | http://http://linkedlifedat... | lld:lhgdn |
lhgdn:association:29782 | lhgdn:umls_code | umls-concept:C0032708 | lld:mappings |
entrez-gene:7389 | lhgdn:associationId | lhgdn:association:29782 | lld:lhgdn |