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PubMed:15122711 / 404-630 JSONTXT

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LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
744 30-46 DiseaseOrPhenotypicFeature denotes Alpers' syndrome MESH:D002549
745 127-131 GeneOrGeneProduct denotes POLG NCBIGene:5428
746 152-162 SequenceVariant denotes Glu873Stop DBSNP:rs121918047

LitCoin-sentences

Id Subject Object Predicate Lexical cue
T4 0-226 Sentence denotes In two unrelated pedigrees of Alpers' syndrome, each affected child was found to carry a homozygous mutation in exon 17 of the POLG locus that led to a Glu873Stop mutation just upstream of the polymerase domain of the protein.

LitCoin-SeqVar

Id Subject Object Predicate Lexical cue
T1 152-161 SequenceVariant denotes Glu873Sto

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T15 38-46 GeneOrGeneProduct denotes syndrome
T16 100-108 GeneOrGeneProduct denotes mutation
T17 127-131 GeneOrGeneProduct denotes POLG
T18 163-171 GeneOrGeneProduct denotes mutation
T19 193-203 GeneOrGeneProduct denotes polymerase
T20 218-225 GeneOrGeneProduct denotes protein

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T11 38-46 GeneOrGeneProduct denotes syndrome
T12 127-131 GeneOrGeneProduct denotes POLG
T13 193-203 GeneOrGeneProduct denotes polymerase
T14 218-225 GeneOrGeneProduct denotes protein

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T8 30-46 DiseaseOrPhenotypicFeature denotes Alpers' syndrome D002549

LitCoin-GeneOrGeneProduct-v3

Id Subject Object Predicate Lexical cue
T5 127-131 GeneOrGeneProduct denotes POLG

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T4 30-46 DiseaseOrPhenotypicFeature denotes Alpers' syndrome 0008758
T5 62-67 DiseaseOrPhenotypicFeature denotes child 0017015

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T9 30-46 DiseaseOrPhenotypicFeature denotes Alpers' syndrome D002549

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T9 30-46 DiseaseOrPhenotypicFeature denotes Alpers' syndrome D002549

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label
T5 127-131 GeneOrGeneProduct denotes POLG
T9 30-46 DiseaseOrPhenotypicFeature denotes Alpers' syndrome D002549
T41160 152-161 SequenceVariant denotes Glu873Sto

sentences

Id Subject Object Predicate Lexical cue
TextSentencer_T4 0-226 Sentence denotes In two unrelated pedigrees of Alpers' syndrome, each affected child was found to carry a homozygous mutation in exon 17 of the POLG locus that led to a Glu873Stop mutation just upstream of the polymerase domain of the protein.
T4 0-226 Sentence denotes In two unrelated pedigrees of Alpers' syndrome, each affected child was found to carry a homozygous mutation in exon 17 of the POLG locus that led to a Glu873Stop mutation just upstream of the polymerase domain of the protein.

PubCasesORDO

Id Subject Object Predicate Lexical cue
AB2 30-46 ORDO:726 denotes Alpers' syndrome

tmVarCorpus

Id Subject Object Predicate Lexical cue
T1 152-162 ProteinMutation:p|SUB|E|873|X denotes Glu873Stop