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PubMed:19365571 / 94-296 JSONTXT

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LitCoin-sentences

Id Subject Object Predicate Lexical cue
T3 0-202 Sentence denotes To identify mutations in the carbohydrate sulfotransferase gene (CHST6) for a Chinese family with macular corneal dystrophy (MCD) and to investigate the histopathological changes in the affected cornea.

LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
5970 29-63 GeneOrGeneProduct denotes carbohydrate sulfotransferase gene NCBIGene:4166
5971 65-70 GeneOrGeneProduct denotes CHST6 NCBIGene:4166
5972 98-123 DiseaseOrPhenotypicFeature denotes macular corneal dystrophy MESH:D003317
5973 125-128 DiseaseOrPhenotypicFeature denotes MCD MESH:D003317

LitCoin_Mondo

Id Subject Object Predicate Lexical cue mondo_id
T3 98-123 DiseaseOrPhenotypicFeature denotes macular corneal dystrophy 0009020
T4 106-123 DiseaseOrPhenotypicFeature denotes corneal dystrophy 0018102

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T5 12-21 GeneOrGeneProduct denotes mutations
T6 29-58 GeneOrGeneProduct denotes carbohydrate sulfotransferase
T7 65-70 GeneOrGeneProduct denotes CHST6

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T3 29-58 GeneOrGeneProduct denotes carbohydrate sulfotransferase
T4 65-70 GeneOrGeneProduct denotes CHST6

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T2 106-123 DiseaseOrPhenotypicFeature denotes corneal dystrophy D003317
T3 125-128 DiseaseOrPhenotypicFeature denotes MCD C537834

LitCoin-GeneOrGeneProduct-v3

Id Subject Object Predicate Lexical cue
T2 29-58 GeneOrGeneProduct denotes carbohydrate sulfotransferase
T3 65-70 GeneOrGeneProduct denotes CHST6

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T2 98-123 DiseaseOrPhenotypicFeature denotes macular corneal dystrophy 0009020
T3 125-128 DiseaseOrPhenotypicFeature denotes MCD 0019754|0015454|0009020

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T2 106-123 DiseaseOrPhenotypicFeature denotes corneal dystrophy D003317

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T2 106-123 DiseaseOrPhenotypicFeature denotes corneal dystrophy D003317

LitCoin-Chemical-MeSH-CHEBI

Id Subject Object Predicate Lexical cue ID:
T1 29-58 ChemicalEntity denotes carbohydrate sulfotransferase C118929

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label ID:
T1 29-58 ChemicalEntity denotes carbohydrate sulfotransferase C118929
T3 65-70 GeneOrGeneProduct denotes CHST6
T69046 29-58 GeneOrGeneProduct denotes carbohydrate sulfotransferase
T59049 106-123 DiseaseOrPhenotypicFeature denotes corneal dystrophy D003317

PMID_GLOBAL

Id Subject Object Predicate Lexical cue mondo_id
T2 98-123 DiseaseOrPhenotypicFeature denotes macular corneal dystrophy 0009020
T3 125-128 DiseaseOrPhenotypicFeature denotes MCD 0009020|0015454|0019754

DisGeNET

Id Subject Object Predicate Lexical cue
T0 65-70 gene:4166 denotes CHST6
T1 98-123 disease:C0024439 denotes macular corneal dystrophy
T2 65-70 gene:4166 denotes CHST6
T3 125-128 disease:C0342793 denotes MCD
T4 65-70 gene:4166 denotes CHST6
T5 125-128 disease:C1636149 denotes MCD
R1 T0 T1 associated_with CHST6,macular corneal dystrophy
R2 T2 T3 associated_with CHST6,MCD
R3 T4 T5 associated_with CHST6,MCD

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
19365571-1#65#70#gene4166 65-70 gene4166 denotes CHST6
19365571-1#125#128#diseaseC1636149 125-128 diseaseC1636149 denotes MCD
65#70#gene4166125#128#diseaseC1636149 19365571-1#65#70#gene4166 19365571-1#125#128#diseaseC1636149 associated_with CHST6,MCD