Source:http://linkedlifedata.com/resource/lhgdn/association:63066
Subject | Predicate | Object | Context |
---|---|---|---|
lhgdn:association:63066 | lhgdn:found_in | pubmed-article:18234697 | lld:lhgdn |
lhgdn:association:63066 | lhgdn:geneRifSource | patients with GRN mutations: have a shorter disease duration (with the exception of FTD-MND); present bvFTLD, language output impairment or with CBS; have parietal lobe dysfunction; and have evidence of asymmetrical brain atrophy on MR imaging. | lld:lhgdn |
lhgdn:association:63066 | lhgdn:mesh_code | D001284 | lld:lhgdn |
lhgdn:association:63066 | lhgdn:associationIdType | http://http://linkedlifedat... | lld:lhgdn |
lhgdn:association:63066 | lhgdn:umls_code | umls-concept:C0333641 | lld:mappings |
entrez-gene:2896 | lhgdn:associationId | lhgdn:association:63066 | lld:lhgdn |