> top > docs > PubMed:19101703 > spans > 0-123 > annotations

PubMed:19101703 / 0-123 JSONTXT

Annnotations TAB JSON ListView MergeView

LitCoin-sentences

Id Subject Object Predicate Lexical cue
T1 0-68 Sentence denotes Study of a Taiwanese family with oculopharyngeal muscular dystrophy.
T2 69-80 Sentence denotes BACKGROUND:

LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
5651 33-67 DiseaseOrPhenotypicFeature denotes oculopharyngeal muscular dystrophy MESH:D039141
5652 81-115 DiseaseOrPhenotypicFeature denotes Oculopharyngeal muscular dystrophy MESH:D039141
5653 117-121 DiseaseOrPhenotypicFeature denotes OPMD MESH:D039141

LitCoin_Mondo

Id Subject Object Predicate Lexical cue mondo_id
T1 33-67 DiseaseOrPhenotypicFeature denotes oculopharyngeal muscular dystrophy 0008116
T2 49-67 DiseaseOrPhenotypicFeature denotes muscular dystrophy 0020121
T3 81-115 DiseaseOrPhenotypicFeature denotes Oculopharyngeal muscular dystrophy 0008116
T4 97-115 DiseaseOrPhenotypicFeature denotes muscular dystrophy 0020121

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T1 117-121 GeneOrGeneProduct denotes OPMD

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T1 117-121 GeneOrGeneProduct denotes OPMD

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T1 33-67 DiseaseOrPhenotypicFeature denotes oculopharyngeal muscular dystrophy D039141
T2 81-115 DiseaseOrPhenotypicFeature denotes Oculopharyngeal muscular dystrophy D039141
T3 117-121 DiseaseOrPhenotypicFeature denotes OPMD D039141

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T1 33-67 DiseaseOrPhenotypicFeature denotes oculopharyngeal muscular dystrophy 0008116
T2 81-115 DiseaseOrPhenotypicFeature denotes Oculopharyngeal muscular dystrophy 0008116
T3 117-121 DiseaseOrPhenotypicFeature denotes OPMD 0008116

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T1 33-67 DiseaseOrPhenotypicFeature denotes oculopharyngeal muscular dystrophy D039141
T2 81-115 DiseaseOrPhenotypicFeature denotes Oculopharyngeal muscular dystrophy D039141
T3 117-121 DiseaseOrPhenotypicFeature denotes OPMD D039141

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T1 33-67 DiseaseOrPhenotypicFeature denotes oculopharyngeal muscular dystrophy D039141
T2 81-115 DiseaseOrPhenotypicFeature denotes Oculopharyngeal muscular dystrophy D039141
T3 117-121 DiseaseOrPhenotypicFeature denotes OPMD D039141

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label
T94756 117-121 DiseaseOrPhenotypicFeature denotes OPMD D039141
T24740 81-115 DiseaseOrPhenotypicFeature denotes Oculopharyngeal muscular dystrophy D039141
T31359 33-67 DiseaseOrPhenotypicFeature denotes oculopharyngeal muscular dystrophy D039141