Source:http://linkedlifedata.com/resource/lhgdn/association:24328
| Subject | Predicate | Object | Context |
|---|---|---|---|
| lhgdn:association:24328 | lhgdn:found_in | pubmed-article:12031624 | lld:lhgdn |
| lhgdn:association:24328 | lhgdn:geneRifSource | two new mutations in the myophosphorylase gene in Italian patients with McArdle?s disease; both were compound heterozygous, with the common mutation at codon 49 (R49X) on the other allele | lld:lhgdn |
| lhgdn:association:24328 | lhgdn:mesh_code | D006012 | lld:lhgdn |
| lhgdn:association:24328 | lhgdn:associationIdType | http://http://linkedlifedat... | lld:lhgdn |
| lhgdn:association:24328 | lhgdn:umls_code | umls-concept:C0017924 | lld:mappings |
| entrez-gene:5837 | lhgdn:associationId | lhgdn:association:24328 | lld:lhgdn |