PubMed:26900322 / 1240-1532 JSONTXT

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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