PubMed:20106987 / 121-295
Annnotations
sentences
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T2 | 0-174 | Sentence | denotes | Ullrich congenital muscular dystrophy (UCMD) is a disabling and life-threatening disorder resulting from either recessive or dominant mutations in genes encoding collagen VI. |
PubmedHPO
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 8-37 | HP_0003741 | denotes | congenital muscular dystrophy |
| T2 | 19-37 | HP_0003560 | denotes | muscular dystrophy |
Allie
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| SS1_20106987_1_0 | 0-37 | expanded | denotes | Ullrich congenital muscular dystrophy |
| SS2_20106987_1_0 | 39-43 | abbr | denotes | UCMD |
| AE1_20106987_1_0 | SS1_20106987_1_0 | SS2_20106987_1_0 | abbreviatedTo | Ullrich congenital muscular dystrophy,UCMD |
PubCasesHPO
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| AB1 | 8-37 | HP:0003741 | denotes | congenital muscular dystrophy |
mondo_disease
| Id | Subject | Object | Predicate | Lexical cue | mondo_id |
|---|---|---|---|---|---|
| T3 | 0-37 | Disease | denotes | Ullrich congenital muscular dystrophy | http://purl.obolibrary.org/obo/MONDO_0000355|http://purl.obolibrary.org/obo/MONDO_0009681 |
| T5 | 39-43 | Disease | denotes | UCMD | http://purl.obolibrary.org/obo/MONDO_0000355 |
HP-phenotype
| Id | Subject | Object | Predicate | Lexical cue | hp_id |
|---|---|---|---|---|---|
| T2 | 8-37 | Phenotype | denotes | congenital muscular dystrophy | HP:0003560 |