PubMed:8755918 / 1017-1219
Annnotations
LitCoin-sentences
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T9 | 0-202 | Sentence | denotes | The demonstration of mutations giving rise to a slightly milder phenotype in A-T raises the interesting question of what range of phenotypes might occur in individuals in whom both mutations are milder. |
LitCoin-entities
| Id | Subject | Object | Predicate | Lexical cue | db_id |
|---|---|---|---|---|---|
| 173 | 77-80 | DiseaseOrPhenotypicFeature | denotes | A-T | MESH:D001260 |
LitCoin-GeneOrGeneProduct-v0
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T24 | 18-30 | GeneOrGeneProduct | denotes | of mutations |
| T25 | 48-56 | GeneOrGeneProduct | denotes | slightly |
| T26 | 81-87 | GeneOrGeneProduct | denotes | raises |
| T27 | 121-126 | GeneOrGeneProduct | denotes | range |
| T28 | 181-190 | GeneOrGeneProduct | denotes | mutations |
LitCoin-MONDO_bioort2019
| Id | Subject | Object | Predicate | Lexical cue | #label |
|---|---|---|---|---|---|
| T8 | 77-80 | DiseaseOrPhenotypicFeature | denotes | A-T | DISEASE |
LitCoin-training-merged
| Id | Subject | Object | Predicate | Lexical cue | #label |
|---|---|---|---|---|---|
| T8 | 77-80 | DiseaseOrPhenotypicFeature | denotes | A-T | DISEASE |
NCBIDiseaseCorpus
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T8 | 77-80 | SpecificDisease:D001260 | denotes | A-T |