PubMed:26900322 / 1240-1532
Annnotations
LitCoin-entities
Id | Subject | Object | Predicate | Lexical cue | db_id |
---|---|---|---|---|---|
11084 | 104-107 | GeneOrGeneProduct | denotes | CFI | NCBIGene:3426 |
11085 | 108-117 | SequenceVariant | denotes | rs7356506 | DBSNP:rs7356506 |
11086 | 121-129 | OrganismTaxon | denotes | patients | NCBITaxon:9606 |
11087 | 135-147 | DiseaseOrPhenotypicFeature | denotes | VKH syndrome | MESH:D014607 |
11088 | 165-173 | DiseaseOrPhenotypicFeature | denotes | cataract | MESH:D002386 |
LitCoin-sentences
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T14 | 0-292 | Sentence | denotes | Furthermore, there were significant decreases in the frequencies of the G allele and GG homozygosity in CFI-rs7356506 in patients with VKH syndrome with complicated cataract compared to the controls (p<0.001, OR=0.357, 95% CI=0.197-0.648; p<0.001, OR=0.273, 95% CI=0.135-0.551, respectively). |
LitCoin_Mondo
Id | Subject | Object | Predicate | Lexical cue | mondo_id |
---|---|---|---|---|---|
T3 | 165-173 | DiseaseOrPhenotypicFeature | denotes | cataract | 0005129 |
LitCoin-SeqVar
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T5 | 108-117 | SequenceVariant | denotes | rs7356506 |
LitCoin-GeneOrGeneProduct-v0
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T16 | 53-64 | GeneOrGeneProduct | denotes | frequencies |
T17 | 139-147 | GeneOrGeneProduct | denotes | syndrome |
T18 | 165-173 | GeneOrGeneProduct | denotes | cataract |
LitCoin-GeneOrGeneProduct-v2
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T9 | 139-147 | GeneOrGeneProduct | denotes | syndrome |
T10 | 165-173 | GeneOrGeneProduct | denotes | cataract |
LitCoin-Disease-MeSH
Id | Subject | Object | Predicate | Lexical cue | originalLabel |
---|---|---|---|---|---|
T10 | 135-147 | DiseaseOrPhenotypicFeature | denotes | VKH syndrome | D014607 |
T11 | 165-173 | DiseaseOrPhenotypicFeature | denotes | cataract | D002386 |
LitCoin-GeneOrGeneProduct-v3
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T8 | 104-107 | GeneOrGeneProduct | denotes | CFI |
LitCoin_Mondo_095
Id | Subject | Object | Predicate | Lexical cue | mondo_id |
---|---|---|---|---|---|
T10 | 135-147 | DiseaseOrPhenotypicFeature | denotes | VKH syndrome | 0018092 |
T11 | 165-173 | DiseaseOrPhenotypicFeature | denotes | cataract | 0005129 |
LitCoin-MeSH-Disease-2
Id | Subject | Object | Predicate | Lexical cue | ID: |
---|---|---|---|---|---|
T8 | 135-147 | DiseaseOrPhenotypicFeature | denotes | VKH syndrome | D014607 |
T9 | 165-173 | DiseaseOrPhenotypicFeature | denotes | cataract | D002386 |
LitCoin-MONDO_bioort2019
Id | Subject | Object | Predicate | Lexical cue | #label |
---|---|---|---|---|---|
T8 | 135-147 | DiseaseOrPhenotypicFeature | denotes | VKH syndrome | D014607 |
T9 | 165-173 | DiseaseOrPhenotypicFeature | denotes | cataract | D002386 |
LitCoin-NCBITaxon-2
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T4 | 121-129 | OrganismTaxon | denotes | patients |
LitCoin-Chemical-MeSH-CHEBI
Id | Subject | Object | Predicate | Lexical cue | ID: |
---|---|---|---|---|---|
T9 | 104-107 | ChemicalEntity | denotes | CFI | C010073 |
LitCoin-training-merged
Id | Subject | Object | Predicate | Lexical cue | #label | ID: |
---|---|---|---|---|---|---|
T9 | 104-107 | ChemicalEntity | denotes | CFI | C010073 | |
T60582 | 104-107 | GeneOrGeneProduct | denotes | CFI | ||
T50868 | 165-173 | DiseaseOrPhenotypicFeature | denotes | cataract | D002386 | |
T12807 | 135-147 | DiseaseOrPhenotypicFeature | denotes | VKH syndrome | D014607 | |
T57425 | 121-129 | OrganismTaxon | denotes | patients | ||
T1460 | 108-117 | SequenceVariant | denotes | rs7356506 |