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PubMed:18945288 / 0-144 JSONTXT

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LitCoin-sentences

Id Subject Object Predicate Lexical cue
T1 0-72 Sentence denotes R58fs mutation in the HGD gene in a family with alkaptonuria in the UAE.

LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
5523 0-5 SequenceVariant denotes R58fs p|FS|R|58||
5524 22-25 GeneOrGeneProduct denotes HGD NCBIGene:3081
5525 48-60 DiseaseOrPhenotypicFeature denotes alkaptonuria MESH:D000474
5526 129-141 DiseaseOrPhenotypicFeature denotes alkaptonuria MESH:D000474

LitCoin_Mondo

Id Subject Object Predicate Lexical cue mondo_id
T1 48-60 DiseaseOrPhenotypicFeature denotes alkaptonuria 0008753
T2 129-141 DiseaseOrPhenotypicFeature denotes alkaptonuria 0008753

LitCoin-SeqVar

Id Subject Object Predicate Lexical cue
T1 0-5 SequenceVariant denotes R58fs

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T1 48-60 GeneOrGeneProduct denotes alkaptonuria
T2 129-141 GeneOrGeneProduct denotes alkaptonuria

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T1 6-14 GeneOrGeneProduct denotes mutation
T2 26-35 GeneOrGeneProduct denotes gene in a
T3 48-60 GeneOrGeneProduct denotes alkaptonuria
T4 101-110 GeneOrGeneProduct denotes determine
T5 129-141 GeneOrGeneProduct denotes alkaptonuria

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T1 48-60 DiseaseOrPhenotypicFeature denotes alkaptonuria D000474
T2 129-141 DiseaseOrPhenotypicFeature denotes alkaptonuria D000474

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T1 48-60 DiseaseOrPhenotypicFeature denotes alkaptonuria 0008753
T2 129-141 DiseaseOrPhenotypicFeature denotes alkaptonuria 0008753

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T1 48-60 DiseaseOrPhenotypicFeature denotes alkaptonuria D000474
T2 129-141 DiseaseOrPhenotypicFeature denotes alkaptonuria D000474

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T1 48-60 DiseaseOrPhenotypicFeature denotes alkaptonuria D000474
T2 129-141 DiseaseOrPhenotypicFeature denotes alkaptonuria D000474

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label
T62351 129-141 DiseaseOrPhenotypicFeature denotes alkaptonuria D000474
T63171 48-60 DiseaseOrPhenotypicFeature denotes alkaptonuria D000474
T18244 0-5 SequenceVariant denotes R58fs

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
18945288-0#22#25#gene3081 22-25 gene3081 denotes HGD
18945288-0#48#60#diseaseC0002066 48-60 diseaseC0002066 denotes alkaptonuria
22#25#gene308148#60#diseaseC0002066 18945288-0#22#25#gene3081 18945288-0#48#60#diseaseC0002066 associated_with HGD,alkaptonuria

tmVarCorpus

Id Subject Object Predicate Lexical cue
T1 0-5 ProteinMutation:p|FS|R|58|| denotes R58fs