PubMed:15241482 / 229-373
Annnotations
LitCoin-entities
| Id | Subject | Object | Predicate | Lexical cue | db_id |
|---|---|---|---|---|---|
| 966 | 26-31 | SequenceVariant | denotes | 55M/L | p|SUB|M|55|L |
| 967 | 36-42 | SequenceVariant | denotes | 192Q/R | p|SUB|Q|192|R |
| 968 | 68-75 | SequenceVariant | denotes | -107C/T | c|SUB|C|-107|T |
| 969 | 140-143 | DiseaseOrPhenotypicFeature | denotes | CHD | MESH:D003327 |
LitCoin-sentences
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T3 | 0-144 | Sentence | denotes | Two coding polymorphisms, 55M/L and 192Q/R, and a promoter variant, -107C/T, has been extensively studied with respect to susceptibility to CHD. |
LitCoin-SeqVar
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 26-29 | SequenceVariant | denotes | 55M |
| T2 | 36-40 | SequenceVariant | denotes | 192Q |
| T3 | 69-73 | SequenceVariant | denotes | 107C |
LitCoin-GeneOrGeneProduct-v0
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T7 | 86-97 | GeneOrGeneProduct | denotes | extensively |
LitCoin-Disease-MeSH
| Id | Subject | Object | Predicate | Lexical cue | originalLabel |
|---|---|---|---|---|---|
| T4 | 140-143 | DiseaseOrPhenotypicFeature | denotes | CHD | D003327 |
LitCoin_Mondo_095
| Id | Subject | Object | Predicate | Lexical cue | mondo_id |
|---|---|---|---|---|---|
| T3 | 140-143 | DiseaseOrPhenotypicFeature | denotes | CHD | 0005010 |
LitCoin-MeSH-Disease-2
| Id | Subject | Object | Predicate | Lexical cue | ID: |
|---|---|---|---|---|---|
| T4 | 140-143 | DiseaseOrPhenotypicFeature | denotes | CHD | D003327 |
LitCoin-MONDO_bioort2019
| Id | Subject | Object | Predicate | Lexical cue | #label |
|---|---|---|---|---|---|
| T3 | 140-143 | DiseaseOrPhenotypicFeature | denotes | CHD | D003327 |
LitCoin-training-merged
| Id | Subject | Object | Predicate | Lexical cue | #label |
|---|---|---|---|---|---|
| T78486 | 140-143 | DiseaseOrPhenotypicFeature | denotes | CHD | D003327 |
| T36969 | 69-73 | SequenceVariant | denotes | 107C | |
| T25380 | 36-40 | SequenceVariant | denotes | 192Q | |
| T73731 | 26-29 | SequenceVariant | denotes | 55M |
DisGeNET5_variant_disease
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| 15241482-2#26#31#geners854560 | 26-31 | geners854560 | denotes | 55M/L |
| 15241482-2#140#143#diseaseC0010068 | 140-143 | diseaseC0010068 | denotes | CHD |
| 26#31#geners854560140#143#diseaseC0010068 | 15241482-2#26#31#geners854560 | 15241482-2#140#143#diseaseC0010068 | associated_with | 55M/L,CHD |