PubMed:26900322 / 1695-1993 JSONTXT

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LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
11094 26-29 GeneOrGeneProduct denotes CFI NCBIGene:3426
11095 82-94 DiseaseOrPhenotypicFeature denotes VKH syndrome MESH:D014607
11096 155-158 GeneOrGeneProduct denotes CFI NCBIGene:3426
11097 159-166 SequenceVariant denotes 7356506 DBSNP:rs7356506
11098 172-184 DiseaseOrPhenotypicFeature denotes VKH syndrome MESH:D014607
11099 242-250 DiseaseOrPhenotypicFeature denotes cataract MESH:D002386
11100 273-280 ChemicalEntity denotes steroid MESH:D013256

LitCoin-sentences

Id Subject Object Predicate Lexical cue
T17 0-298 Sentence denotes Our results indicate that CFI polymorphisms are not significantly associated with VKH syndrome; nevertheless, we identified a trend for the association of CFI-7356506 with VKH syndrome that depends on the recurrent status and the complicated cataract status but not on the steroid-sensitive status.

LitCoin_Mondo

Id Subject Object Predicate Lexical cue mondo_id
T4 242-250 DiseaseOrPhenotypicFeature denotes cataract 0005129

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T20 86-94 GeneOrGeneProduct denotes syndrome
T21 176-184 GeneOrGeneProduct denotes syndrome
T22 242-250 GeneOrGeneProduct denotes cataract

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T12 86-94 GeneOrGeneProduct denotes syndrome
T13 176-184 GeneOrGeneProduct denotes syndrome
T14 242-250 GeneOrGeneProduct denotes cataract

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T13 82-94 DiseaseOrPhenotypicFeature denotes VKH syndrome D014607
T14 172-184 DiseaseOrPhenotypicFeature denotes VKH syndrome D014607
T15 205-214 DiseaseOrPhenotypicFeature denotes recurrent D012008
T16 242-250 DiseaseOrPhenotypicFeature denotes cataract D002386

LitCoin-GeneOrGeneProduct-v3

Id Subject Object Predicate Lexical cue
T10 26-29 GeneOrGeneProduct denotes CFI
T11 155-158 GeneOrGeneProduct denotes CFI

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T14 82-94 DiseaseOrPhenotypicFeature denotes VKH syndrome 0018092
T15 172-184 DiseaseOrPhenotypicFeature denotes VKH syndrome 0018092
T16 242-250 DiseaseOrPhenotypicFeature denotes cataract 0005129
T17 281-290 DiseaseOrPhenotypicFeature denotes sensitive 0000605

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T11 82-94 DiseaseOrPhenotypicFeature denotes VKH syndrome D014607
T12 172-184 DiseaseOrPhenotypicFeature denotes VKH syndrome D014607
T13 242-250 DiseaseOrPhenotypicFeature denotes cataract D002386

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T11 82-94 DiseaseOrPhenotypicFeature denotes VKH syndrome D014607
T12 172-184 DiseaseOrPhenotypicFeature denotes VKH syndrome D014607
T13 242-250 DiseaseOrPhenotypicFeature denotes cataract D002386

LitCoin-Chemical-MeSH-CHEBI

Id Subject Object Predicate Lexical cue ID:
T13 26-29 ChemicalEntity denotes CFI C010073
T14 155-158 ChemicalEntity denotes CFI C010073
T15 273-280 ChemicalEntity denotes steroid D013256|http://purl.obolibrary.org/obo/CHEBI_35341

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label ID:
T15 273-280 ChemicalEntity denotes steroid http://purl.obolibrary.org/obo/CHEBI_35341|D013256
T14 155-158 ChemicalEntity denotes CFI C010073
T13 26-29 ChemicalEntity denotes CFI C010073
T11 155-158 GeneOrGeneProduct denotes CFI
T27514 26-29 GeneOrGeneProduct denotes CFI
T66997 242-250 DiseaseOrPhenotypicFeature denotes cataract D002386
T364 172-184 DiseaseOrPhenotypicFeature denotes VKH syndrome D014607
T9570 82-94 DiseaseOrPhenotypicFeature denotes VKH syndrome D014607