PubMed:29049388 / 1647-1864 JSONTXT

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LitCoin-entities-OrganismTaxon-PD

Id Subject Object Predicate Lexical cue db_id
T8 43-48 OrganismTaxon denotes mouse NCBItxid:10090|NCBItxid:10088
T10 114-119 OrganismTaxon denotes human NCBItxid:9606
T11 202-207 OrganismTaxon denotes human NCBItxid:9606

LitCoin-sentences

Id Subject Object Predicate Lexical cue
T15 0-217 Sentence denotes In conclusion, the inducible R140Q-podocin mouse model is an auspicious model of the most common genetic cause of human nephrotic syndrome, with a spontaneous disease course strongly reminiscent of the human disorder.

LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
13494 29-34 SequenceVariant denotes R140Q p|SUB|R|140|Q
13495 35-42 GeneOrGeneProduct denotes podocin NCBIGene:170484
13496 43-48 OrganismTaxon denotes mouse NCBITaxon:10090
13497 114-119 OrganismTaxon denotes human NCBITaxon:9606
13498 120-138 DiseaseOrPhenotypicFeature denotes nephrotic syndrome MESH:D009404
13499 202-207 OrganismTaxon denotes human NCBITaxon:9606

LitCoin_Mondo

Id Subject Object Predicate Lexical cue mondo_id
T5 120-138 DiseaseOrPhenotypicFeature denotes nephrotic syndrome 0005377

LitCoin-SeqVar

Id Subject Object Predicate Lexical cue
T7 29-34 SequenceVariant denotes R140Q

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T38 19-28 GeneOrGeneProduct denotes inducible
T39 35-42 GeneOrGeneProduct denotes podocin
T40 130-138 GeneOrGeneProduct denotes syndrome

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T22 19-28 GeneOrGeneProduct denotes inducible
T23 35-42 GeneOrGeneProduct denotes podocin
T24 130-138 GeneOrGeneProduct denotes syndrome

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T14 120-138 DiseaseOrPhenotypicFeature denotes nephrotic syndrome D009404
T15 159-166 DiseaseOrPhenotypicFeature denotes disease D004194

LitCoin-GeneOrGeneProduct-v3

Id Subject Object Predicate Lexical cue
T9 35-42 GeneOrGeneProduct denotes podocin

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T12 120-138 DiseaseOrPhenotypicFeature denotes nephrotic syndrome 0005377

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T13 120-138 DiseaseOrPhenotypicFeature denotes nephrotic syndrome D009404
T14 159-166 DiseaseOrPhenotypicFeature denotes disease D004194

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T9 120-138 DiseaseOrPhenotypicFeature denotes nephrotic syndrome D009404

LitCoin-NCBITaxon-2

Id Subject Object Predicate Lexical cue
T5 43-48 OrganismTaxon denotes mouse
T6 114-119 OrganismTaxon denotes human
T7 202-207 OrganismTaxon denotes human

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label
T9 35-42 GeneOrGeneProduct denotes podocin
T45427 120-138 DiseaseOrPhenotypicFeature denotes nephrotic syndrome D009404
T23115 202-207 OrganismTaxon denotes human
T40596 114-119 OrganismTaxon denotes human
T64328 43-48 OrganismTaxon denotes mouse
T74446 29-34 SequenceVariant denotes R140Q