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PubMed:21126715 / 293-522 JSONTXT

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LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
8369 17-22 GeneOrGeneProduct denotes BSCL2 NCBIGene:26580
8370 51-55 DiseaseOrPhenotypicFeature denotes CGL2 MESH:D052497
8371 86-90 DiseaseOrPhenotypicFeature denotes CGL1 MESH:D052497
8372 173-196 DiseaseOrPhenotypicFeature denotes intellectual impairment MESH:D008607
8373 214-228 DiseaseOrPhenotypicFeature denotes cardiomyopathy MESH:D009202

LitCoin-sentences

Id Subject Object Predicate Lexical cue
T3 0-229 Sentence denotes Mutations in the BSCL2 gene are known to result in CGL2, a more severe phenotype than CGL1, with earlier onset, more extensive fat loss and biochemical changes, more severe intellectual impairment, and more severe cardiomyopathy.

LitCoin_Mondo

Id Subject Object Predicate Lexical cue mondo_id
T11 214-228 DiseaseOrPhenotypicFeature denotes cardiomyopathy 0004994

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T7 0-9 GeneOrGeneProduct denotes Mutations
T8 17-22 GeneOrGeneProduct denotes BSCL2
T9 51-55 GeneOrGeneProduct denotes CGL2
T10 86-90 GeneOrGeneProduct denotes CGL1
T11 117-126 GeneOrGeneProduct denotes extensive

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T5 17-22 GeneOrGeneProduct denotes BSCL2
T6 51-55 GeneOrGeneProduct denotes CGL2
T7 86-90 GeneOrGeneProduct denotes CGL1

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T5 214-228 DiseaseOrPhenotypicFeature denotes cardiomyopathy D009202

LitCoin-GeneOrGeneProduct-v3

Id Subject Object Predicate Lexical cue
T2 17-22 GeneOrGeneProduct denotes BSCL2
T3 51-55 GeneOrGeneProduct denotes CGL2
T4 86-90 GeneOrGeneProduct denotes CGL1

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T5 51-55 DiseaseOrPhenotypicFeature denotes CGL2 0010020
T6 86-90 DiseaseOrPhenotypicFeature denotes CGL1 0012071
T7 214-228 DiseaseOrPhenotypicFeature denotes cardiomyopathy 0004994

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T5 51-55 DiseaseOrPhenotypicFeature denotes CGL2 DISEASE
T6 86-90 DiseaseOrPhenotypicFeature denotes CGL1 DISEASE
T7 173-196 DiseaseOrPhenotypicFeature denotes intellectual impairment DISEASE
T8 214-228 DiseaseOrPhenotypicFeature denotes cardiomyopathy D009202

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T5 51-55 DiseaseOrPhenotypicFeature denotes CGL2 DISEASE
T6 86-90 DiseaseOrPhenotypicFeature denotes CGL1 DISEASE
T7 173-196 DiseaseOrPhenotypicFeature denotes intellectual impairment DISEASE
T8 214-228 DiseaseOrPhenotypicFeature denotes cardiomyopathy D009202

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label
T4 86-90 GeneOrGeneProduct denotes CGL1
T3 51-55 GeneOrGeneProduct denotes CGL2
T2 17-22 GeneOrGeneProduct denotes BSCL2
T8 214-228 DiseaseOrPhenotypicFeature denotes cardiomyopathy D009202
T16413 173-196 DiseaseOrPhenotypicFeature denotes intellectual impairment DISEASE
T11558 86-90 DiseaseOrPhenotypicFeature denotes CGL1 DISEASE
T35338 51-55 DiseaseOrPhenotypicFeature denotes CGL2 DISEASE

DisGeNET

Id Subject Object Predicate Lexical cue
T0 17-22 gene:26580 denotes BSCL2
T1 214-228 disease:C0878544 denotes cardiomyopathy
T2 86-90 gene:3002 denotes CGL1
T3 173-196 disease:C0683322 denotes intellectual impairment
T4 86-90 gene:3002 denotes CGL1
T5 214-228 disease:C0878544 denotes cardiomyopathy
R1 T0 T1 associated_with BSCL2,cardiomyopathy
R2 T2 T3 associated_with CGL1,intellectual impairment
R3 T4 T5 associated_with CGL1,cardiomyopathy

PubmedHPO

Id Subject Object Predicate Lexical cue
T5 173-196 HP_0100543 denotes intellectual impairment
T6 214-228 HP_0001638 denotes cardiomyopathy

PubCasesHPO

Id Subject Object Predicate Lexical cue
AB2 214-228 HP:0001638 denotes cardiomyopathy