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PubMed:19394258 / 0-101 JSONTXT

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LitCoin-sentences

Id Subject Object Predicate Lexical cue
T1 0-101 Sentence denotes The first founder DGUOK mutation associated with hepatocerebral mitochondrial DNA depletion syndrome.

LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
6019 18-23 GeneOrGeneProduct denotes DGUOK NCBIGene:1716
6020 49-100 DiseaseOrPhenotypicFeature denotes hepatocerebral mitochondrial DNA depletion syndrome MESH:C580039

LitCoin_Mondo

Id Subject Object Predicate Lexical cue mondo_id
T1 64-100 DiseaseOrPhenotypicFeature denotes mitochondrial DNA depletion syndrome 0018158

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T1 18-23 GeneOrGeneProduct denotes DGUOK
T2 24-32 GeneOrGeneProduct denotes mutation
T3 64-77 GeneOrGeneProduct denotes mitochondrial
T4 82-91 GeneOrGeneProduct denotes depletion
T5 92-100 GeneOrGeneProduct denotes syndrome

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T1 18-23 GeneOrGeneProduct denotes DGUOK
T2 64-77 GeneOrGeneProduct denotes mitochondrial
T3 92-100 GeneOrGeneProduct denotes syndrome

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T1 49-100 DiseaseOrPhenotypicFeature denotes hepatocerebral mitochondrial DNA depletion syndrome C580039

LitCoin-GeneOrGeneProduct-v3

Id Subject Object Predicate Lexical cue
T1 18-23 GeneOrGeneProduct denotes DGUOK

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T1 64-100 DiseaseOrPhenotypicFeature denotes mitochondrial DNA depletion syndrome 0018158

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T1 49-100 DiseaseOrPhenotypicFeature denotes hepatocerebral mitochondrial DNA depletion syndrome C580039

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T1 49-100 DiseaseOrPhenotypicFeature denotes hepatocerebral mitochondrial DNA depletion syndrome C580039

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label
T93033 18-23 GeneOrGeneProduct denotes DGUOK
T91302 49-100 DiseaseOrPhenotypicFeature denotes hepatocerebral mitochondrial DNA depletion syndrome C580039

DisGeNET

Id Subject Object Predicate Lexical cue
T0 18-23 gene:1716 denotes DGUOK
T1 49-100 disease:C3711385 denotes hepatocerebral mitochondrial DNA depletion syndrome
R1 T0 T1 associated_with DGUOK,hepatocerebral mitochondrial DNA depletion syndrome

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
19394258-0#18#23#gene1716 18-23 gene1716 denotes DGUOK
19394258-0#49#100#diseaseC3711385 49-100 diseaseC3711385 denotes hepatocerebral mitochondrial DNA depletion syndrome
18#23#gene171649#100#diseaseC3711385 19394258-0#18#23#gene1716 19394258-0#49#100#diseaseC3711385 associated_with DGUOK,hepatocerebral mitochondrial DNA depletion syndrome