PubMed:18470323 / 114-242
Annnotations
LitCoin-sentences
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T3 | 0-128 | Sentence | denotes | To report the clinical, ophthalmic, and genetic characteristics for lattice corneal dystrophy type I (LCDI) in a Chilean family. |
LitCoin-entities
| Id | Subject | Object | Predicate | Lexical cue | db_id |
|---|---|---|---|---|---|
| 5080 | 68-100 | DiseaseOrPhenotypicFeature | denotes | lattice corneal dystrophy type I | MESH:C537881 |
| 5081 | 102-106 | DiseaseOrPhenotypicFeature | denotes | LCDI | MESH:C537881 |
LitCoin_Mondo
| Id | Subject | Object | Predicate | Lexical cue | mondo_id |
|---|---|---|---|---|---|
| T4 | 68-100 | DiseaseOrPhenotypicFeature | denotes | lattice corneal dystrophy type I | 0007380 |
| T5 | 68-93 | DiseaseOrPhenotypicFeature | denotes | lattice corneal dystrophy | 0004686 |
| T6 | 76-93 | DiseaseOrPhenotypicFeature | denotes | corneal dystrophy | 0018102 |
LitCoin-GeneOrGeneProduct-v2
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T4 | 94-100 | GeneOrGeneProduct | denotes | type I |
LitCoin-GeneOrGeneProduct-v0
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T5 | 94-100 | GeneOrGeneProduct | denotes | type I |
| T6 | 108-112 | GeneOrGeneProduct | denotes | in a |
LitCoin-Disease-MeSH
| Id | Subject | Object | Predicate | Lexical cue | originalLabel |
|---|---|---|---|---|---|
| T2 | 76-93 | DiseaseOrPhenotypicFeature | denotes | corneal dystrophy | D003317 |
LitCoin_Mondo_095
| Id | Subject | Object | Predicate | Lexical cue | mondo_id |
|---|---|---|---|---|---|
| T2 | 68-100 | DiseaseOrPhenotypicFeature | denotes | lattice corneal dystrophy type I | 0007380 |
| T3 | 102-106 | DiseaseOrPhenotypicFeature | denotes | LCDI | 0007380 |
PMID_GLOBAL
| Id | Subject | Object | Predicate | Lexical cue | mondo_id |
|---|---|---|---|---|---|
| T2 | 68-100 | DiseaseOrPhenotypicFeature | denotes | lattice corneal dystrophy type I | 0007380 |
| T3 | 102-106 | DiseaseOrPhenotypicFeature | denotes | LCDI | 0007380 |
LitCoin-MeSH-Disease-2
| Id | Subject | Object | Predicate | Lexical cue | ID: |
|---|---|---|---|---|---|
| T2 | 76-93 | DiseaseOrPhenotypicFeature | denotes | corneal dystrophy | D003317 |
| T3 | 102-106 | DiseaseOrPhenotypicFeature | denotes | LCDI | DISEASE |
LitCoin-MONDO_bioort2019
| Id | Subject | Object | Predicate | Lexical cue | #label |
|---|---|---|---|---|---|
| T2 | 68-100 | DiseaseOrPhenotypicFeature | denotes | lattice corneal dystrophy type I | C537881 |
| T3 | 102-106 | DiseaseOrPhenotypicFeature | denotes | LCDI | DISEASE |
LitCoin-training-merged
| Id | Subject | Object | Predicate | Lexical cue | #label |
|---|---|---|---|---|---|
| T62723 | 102-106 | DiseaseOrPhenotypicFeature | denotes | LCDI | DISEASE |
| T84989 | 68-100 | DiseaseOrPhenotypicFeature | denotes | lattice corneal dystrophy type I | C537881 |
sentences
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| TextSentencer_T3 | 0-128 | Sentence | denotes | To report the clinical, ophthalmic, and genetic characteristics for lattice corneal dystrophy type I (LCDI) in a Chilean family. |
| T3 | 0-128 | Sentence | denotes | To report the clinical, ophthalmic, and genetic characteristics for lattice corneal dystrophy type I (LCDI) in a Chilean family. |
PubCasesHPO
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| AB1 | 68-93 | HP:0001149 | denotes | lattice corneal dystrophy |
PubCasesORDO
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| AB1 | 68-100 | ORDO:98964 | denotes | lattice corneal dystrophy type I |
| AB2 | 102-106 | ORDO:98964 | denotes | LCDI |