PubMed:20846357 / 1823-1949 JSONTXT

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LitCoin-sentences

Id Subject Object Predicate Lexical cue
T19 0-126 Sentence denotes This study has identified a new heterozygous de novo mutation in the Cx26 gene (c.263C>T; p.Ala88Val) leading to KID syndrome.

LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
8084 69-73 GeneOrGeneProduct denotes Cx26 NCBIGene:2706
8085 80-88 SequenceVariant denotes c.263C>T c|SUB|C|263|T
8086 90-100 SequenceVariant denotes p.Ala88Val p|SUB|A|88|V
8087 113-125 DiseaseOrPhenotypicFeature denotes KID syndrome MESH:C536168

LitCoin_Mondo

Id Subject Object Predicate Lexical cue mondo_id
T17 113-125 DiseaseOrPhenotypicFeature denotes KID syndrome 0018781

LitCoin-SeqVar

Id Subject Object Predicate Lexical cue
T4 80-88 SequenceVariant denotes c.263C>T
T5 90-100 SequenceVariant denotes p.Ala88Val

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T38 53-61 GeneOrGeneProduct denotes mutation
T39 69-73 GeneOrGeneProduct denotes Cx26
T40 117-125 GeneOrGeneProduct denotes syndrome

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T25 69-73 GeneOrGeneProduct denotes Cx26
T26 117-125 GeneOrGeneProduct denotes syndrome

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T15 113-125 DiseaseOrPhenotypicFeature denotes KID syndrome C536168

LitCoin-GeneOrGeneProduct-v3

Id Subject Object Predicate Lexical cue
T10 69-73 GeneOrGeneProduct denotes Cx26

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T20 113-125 DiseaseOrPhenotypicFeature denotes KID syndrome 0018781

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T21 113-125 DiseaseOrPhenotypicFeature denotes KID syndrome C536168

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T20 113-125 DiseaseOrPhenotypicFeature denotes KID syndrome C536168

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label
T10 69-73 GeneOrGeneProduct denotes Cx26
T20 113-125 DiseaseOrPhenotypicFeature denotes KID syndrome C536168
T42879 90-100 SequenceVariant denotes p.Ala88Val
T46122 80-88 SequenceVariant denotes c.263C>T

sentences

Id Subject Object Predicate Lexical cue
TextSentencer_T19 0-126 Sentence denotes This study has identified a new heterozygous de novo mutation in the Cx26 gene (c.263C>T; p.Ala88Val) leading to KID syndrome.
T19 0-126 Sentence denotes This study has identified a new heterozygous de novo mutation in the Cx26 gene (c.263C>T; p.Ala88Val) leading to KID syndrome.

PubCasesORDO

Id Subject Object Predicate Lexical cue
AB4 113-125 ORDO:477 denotes KID syndrome

tmVarCorpus

Id Subject Object Predicate Lexical cue
T4 80-88 DNAMutation:c|SUB|C|263|T denotes c.263C>T
T5 90-100 ProteinMutation:p|SUB|A|88|V denotes p.Ala88Val