Source: ALL
Gene | Score gda | Association Type | Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||||
---|---|---|---|---|---|---|---|---|---|---|---|
|
0.700 | GeneticVariation | disease | UNIPROT | Hereditary cerebral hemorrhage with amyloidosis associated with the E693K mutation of APP. | 20697050 | 2010 | ||||
|
0.700 | Biomarker | disease | GENOMICS_ENGLAND | Iowa variant of familial Alzheimer's disease: accumulation of posttranslationally modified AbetaD23N in parenchymal and cerebrovascular amyloid deposits. | 20228223 | 2010 | ||||
|
0.700 | GeneticVariation | disease | UNIPROT | A novel AbetaPP mutation exclusively associated with cerebral amyloid angiopathy. | 16178030 | 2005 | ||||
|
0.700 | GeneticVariation | disease | UNIPROT | Hemorrhagic stroke associated with the Iowa amyloid precursor protein mutation. | 12654973 | 2003 | ||||
|
0.700 | GeneticVariation | disease | UNIPROT | Novel amyloid precursor protein mutation in an Iowa family with dementia and severe cerebral amyloid angiopathy. | 11409420 | 2001 | ||||
|
0.700 | Biomarker | disease | CTD_human | Substitutions at codon 22 of Alzheimer's abeta peptide induce diverse conformational changes and apoptotic effects in human cerebral endothelial cells. | 10821838 | 2000 | ||||
|
0.700 | Biomarker | disease | GENOMICS_ENGLAND | Mutation of the Alzheimer's disease amyloid gene in hereditary cerebral hemorrhage, Dutch type. | 2111584 | 1990 | ||||
|
0.700 | Biomarker | disease | CTD_human | Mutation of the Alzheimer's disease amyloid gene in hereditary cerebral hemorrhage, Dutch type. | 2111584 | 1990 | ||||
|
0.700 | GeneticVariation | disease | UNIPROT | Mutation of the Alzheimer's disease amyloid gene in hereditary cerebral hemorrhage, Dutch type. | 2111584 | 1990 | ||||
|
0.700 | CausalMutation | disease | CLINVAR |