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PubMed:25054547 / 0-179 JSONTXT

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LitCoin-sentences

Id Subject Object Predicate Lexical cue
T1 0-142 Sentence denotes Characterization of a novel BCHE "silent" allele: point mutation (p.Val204Asp) causes loss of activity and prolonged apnea with suxamethonium.

LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
10153 28-32 GeneOrGeneProduct denotes BCHE NCBIGene:590
10154 66-77 SequenceVariant denotes p.Val204Asp p|SUB|V|204|D
10155 117-122 DiseaseOrPhenotypicFeature denotes apnea MESH:D001049
10156 128-141 ChemicalEntity denotes suxamethonium MESH:D013390
10157 143-175 DiseaseOrPhenotypicFeature denotes Butyrylcholinesterase deficiency MESH:C537417

LitCoin_Mondo

Id Subject Object Predicate Lexical cue mondo_id
T1 143-175 DiseaseOrPhenotypicFeature denotes Butyrylcholinesterase deficiency 0015270

LitCoin-SeqVar

Id Subject Object Predicate Lexical cue
T1 66-77 SequenceVariant denotes p.Val204Asp

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T1 22-27 GeneOrGeneProduct denotes novel
T2 28-32 GeneOrGeneProduct denotes BCHE
T3 143-164 GeneOrGeneProduct denotes Butyrylcholinesterase

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T1 22-27 GeneOrGeneProduct denotes novel
T2 28-32 GeneOrGeneProduct denotes BCHE
T3 50-55 GeneOrGeneProduct denotes point
T4 56-64 GeneOrGeneProduct denotes mutation
T5 94-102 GeneOrGeneProduct denotes activity
T6 143-164 GeneOrGeneProduct denotes Butyrylcholinesterase

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T1 117-122 DiseaseOrPhenotypicFeature denotes apnea D001049
T2 143-175 DiseaseOrPhenotypicFeature denotes Butyrylcholinesterase deficiency C537417

LitCoin-GeneOrGeneProduct-v3

Id Subject Object Predicate Lexical cue
T1 28-32 GeneOrGeneProduct denotes BCHE
T2 143-164 GeneOrGeneProduct denotes Butyrylcholinesterase

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T1 143-175 DiseaseOrPhenotypicFeature denotes Butyrylcholinesterase deficiency 0015270

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T1 117-122 DiseaseOrPhenotypicFeature denotes apnea D001049
T2 143-175 DiseaseOrPhenotypicFeature denotes Butyrylcholinesterase deficiency C537417

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T1 117-122 DiseaseOrPhenotypicFeature denotes apnea D001049
T2 143-175 DiseaseOrPhenotypicFeature denotes Butyrylcholinesterase deficiency C537417

LitCoin-Chemical-MeSH-CHEBI

Id Subject Object Predicate Lexical cue ID:
T1 128-141 ChemicalEntity denotes suxamethonium D013390|http://purl.obolibrary.org/obo/CHEBI_45652
T3 143-175 ChemicalEntity denotes Butyrylcholinesterase deficiency C537417

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label ID:
T3 143-175 ChemicalEntity denotes Butyrylcholinesterase deficiency C537417
T1 128-141 ChemicalEntity denotes suxamethonium http://purl.obolibrary.org/obo/CHEBI_45652|D013390
T2 143-164 GeneOrGeneProduct denotes Butyrylcholinesterase
T44130 28-32 GeneOrGeneProduct denotes BCHE
T57186 143-175 DiseaseOrPhenotypicFeature denotes Butyrylcholinesterase deficiency C537417
T88658 117-122 DiseaseOrPhenotypicFeature denotes apnea D001049
T10402 66-77 SequenceVariant denotes p.Val204Asp

sentences

Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-142 Sentence denotes Characterization of a novel BCHE "silent" allele: point mutation (p.Val204Asp) causes loss of activity and prolonged apnea with suxamethonium.
T1 0-142 Sentence denotes Characterization of a novel BCHE "silent" allele: point mutation (p.Val204Asp) causes loss of activity and prolonged apnea with suxamethonium.

PubCasesHPO

Id Subject Object Predicate Lexical cue
TI1 117-122 HP:0002104 denotes apnea

PubCasesORDO

Id Subject Object Predicate Lexical cue
AB1 143-175 ORDO:132 denotes Butyrylcholinesterase deficiency