Statements in which the resource exists.
SubjectPredicateObjectContext
lhgdn:association:63066lhgdn:found_inpubmed-article:18234697lld:lhgdn
lhgdn:association:63066lhgdn:geneRifSourcepatients 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:63066lhgdn:mesh_codeD001284lld:lhgdn
lhgdn:association:63066lhgdn:associationIdTypehttp://http://linkedlifedat...lld:lhgdn
lhgdn:association:63066lhgdn:umls_codeumls-concept:C0333641lld:mappings
entrez-gene:2896lhgdn:associationIdlhgdn:association:63066lld:lhgdn