Source:http://linkedlifedata.com/resource/lhgdn/association:28453
Subject | Predicate | Object | Context |
---|---|---|---|
lhgdn:association:28453 | lhgdn:found_in | pubmed-article:19021637 | lld:lhgdn |
lhgdn:association:28453 | lhgdn:geneRifSource | the novel Metachromatic leukodystrophy- causing mutations in the exons 2, 5 and even in 8 of the ARSA gene described here can be classified as severe type 0, leading in homozygosity to the late infantile form Metachromatic leukodystrophy | lld:lhgdn |
lhgdn:association:28453 | lhgdn:mesh_code | D007966 | lld:lhgdn |
lhgdn:association:28453 | lhgdn:associationIdType | http://http://linkedlifedat... | lld:lhgdn |
lhgdn:association:28453 | lhgdn:umls_code | umls-concept:C2713319 | lld:mappings |
entrez-gene:410 | lhgdn:associationId | lhgdn:association:28453 | lld:lhgdn |