PubMed:11087738 / 182-318
Annnotations
sentences
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T2 | 0-136 | Sentence | denotes | Gerstmann-Sträussler-Scheinker disease (GSS) is a cerebral amyloidosis associated with mutations in the prion protein (PrP) gene (PRNP). |
PubCasesHPO
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| AB1 | 59-70 | HP:0011034 | denotes | amyloidosis |
mondo_disease
| Id | Subject | Object | Predicate | Lexical cue | mondo_id |
|---|---|---|---|---|---|
| T3 | 0-38 | Disease | denotes | Gerstmann-Sträussler-Scheinker disease | http://purl.obolibrary.org/obo/MONDO_0007656 |
| T4 | 40-43 | Disease | denotes | GSS | http://purl.obolibrary.org/obo/MONDO_0007656 |
| T5 | 59-70 | Disease | denotes | amyloidosis | http://purl.obolibrary.org/obo/MONDO_0019065 |
HP-phenotype
| Id | Subject | Object | Predicate | Lexical cue | hp_id |
|---|---|---|---|---|---|
| T1 | 59-70 | Phenotype | denotes | amyloidosis | HP:0011034 |