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PubMed:19101703 / 623-753 JSONTXT

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LitCoin-sentences

Id Subject Object Predicate Lexical cue
T10 0-130 Sentence denotes Ten subjects with OPMD (6 symptomatic and 4 asymptomatic) within the Taiwanese family carried a novel mutation in the PABPN1 gene.

LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
5663 18-22 DiseaseOrPhenotypicFeature denotes OPMD MESH:D039141
5664 118-124 GeneOrGeneProduct denotes PABPN1 NCBIGene:8106

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T13 18-22 GeneOrGeneProduct denotes OPMD
T14 96-101 GeneOrGeneProduct denotes novel
T15 118-124 GeneOrGeneProduct denotes PABPN1

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T18 18-22 GeneOrGeneProduct denotes OPMD
T19 38-43 GeneOrGeneProduct denotes and 4
T20 96-101 GeneOrGeneProduct denotes novel
T21 102-110 GeneOrGeneProduct denotes mutation
T22 118-124 GeneOrGeneProduct denotes PABPN1

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T8 18-22 DiseaseOrPhenotypicFeature denotes OPMD D039141

LitCoin-GeneOrGeneProduct-v3

Id Subject Object Predicate Lexical cue
T6 118-124 GeneOrGeneProduct denotes PABPN1

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T7 18-22 DiseaseOrPhenotypicFeature denotes OPMD 0008116

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T8 18-22 DiseaseOrPhenotypicFeature denotes OPMD D039141

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T8 18-22 DiseaseOrPhenotypicFeature denotes OPMD D039141

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label
T87175 118-124 GeneOrGeneProduct denotes PABPN1
T17787 18-22 DiseaseOrPhenotypicFeature denotes OPMD D039141

DisGeNET

Id Subject Object Predicate Lexical cue
T0 118-124 gene:8106 denotes PABPN1
T1 18-22 disease:C0270952 denotes OPMD
R1 T0 T1 associated_with PABPN1,OPMD

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
19101703-6#118#124#gene8106 118-124 gene8106 denotes PABPN1
19101703-6#18#22#diseaseC0270952 18-22 diseaseC0270952 denotes OPMD
118#124#gene810618#22#diseaseC0270952 19101703-6#118#124#gene8106 19101703-6#18#22#diseaseC0270952 associated_with PABPN1,OPMD