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PubMed:18672102 / 182-331 JSONTXT

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LitCoin-sentences

Id Subject Object Predicate Lexical cue
T3 0-149 Sentence denotes However, the prevalence of GATA4 mutations in CHD and the correlation between the GATA4 genotype and CHD phenotype have not been extensively studied.

LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
5350 27-32 GeneOrGeneProduct denotes GATA4 NCBIGene:2626
5351 46-49 DiseaseOrPhenotypicFeature denotes CHD MESH:D006331
5352 82-87 GeneOrGeneProduct denotes GATA4 NCBIGene:2626
5353 101-104 DiseaseOrPhenotypicFeature denotes CHD MESH:D006331

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T7 27-32 GeneOrGeneProduct denotes GATA4
T8 33-42 GeneOrGeneProduct denotes mutations
T9 82-87 GeneOrGeneProduct denotes GATA4
T10 129-140 GeneOrGeneProduct denotes extensively

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T5 27-32 GeneOrGeneProduct denotes GATA4
T6 82-87 GeneOrGeneProduct denotes GATA4

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T4 46-49 DiseaseOrPhenotypicFeature denotes CHD D006330
T5 101-104 DiseaseOrPhenotypicFeature denotes CHD D006330

LitCoin-GeneOrGeneProduct-v3

Id Subject Object Predicate Lexical cue
T3 27-32 GeneOrGeneProduct denotes GATA4
T4 82-87 GeneOrGeneProduct denotes GATA4

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T5 46-49 DiseaseOrPhenotypicFeature denotes CHD 0005010|0005453
T7 101-104 DiseaseOrPhenotypicFeature denotes CHD 0005010|0005453

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T4 46-49 DiseaseOrPhenotypicFeature denotes CHD D006330
T5 101-104 DiseaseOrPhenotypicFeature denotes CHD D006330

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T4 46-49 DiseaseOrPhenotypicFeature denotes CHD D006330
T5 101-104 DiseaseOrPhenotypicFeature denotes CHD D006330

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label
T4 82-87 GeneOrGeneProduct denotes GATA4
T3 27-32 GeneOrGeneProduct denotes GATA4
T16585 101-104 DiseaseOrPhenotypicFeature denotes CHD D006330
T13053 46-49 DiseaseOrPhenotypicFeature denotes CHD D006330

DisGeNET

Id Subject Object Predicate Lexical cue
T6 27-32 gene:2626 denotes GATA4
T7 46-49 disease:C0010068 denotes CHD
T8 82-87 gene:2626 denotes GATA4
T9 101-104 disease:C0010068 denotes CHD
T10 82-87 gene:2626 denotes GATA4
T11 46-49 disease:C0010068 denotes CHD
T12 27-32 gene:2626 denotes GATA4
T13 101-104 disease:C0010068 denotes CHD
R4 T6 T7 associated_with GATA4,CHD
R5 T8 T9 associated_with GATA4,CHD
R6 T10 T11 associated_with GATA4,CHD
R7 T12 T13 associated_with GATA4,CHD