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PubMed:17166870 / 0-110 JSONTXT

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LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
3693 23-31 GeneOrGeneProduct denotes endoglin NCBIGene:2022
3694 54-72 DiseaseOrPhenotypicFeature denotes systemic sclerosis MESH:D012595

LitCoin_Mondo

Id Subject Object Predicate Lexical cue mondo_id
T1 54-72 DiseaseOrPhenotypicFeature denotes systemic sclerosis 0005100

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T1 23-31 GeneOrGeneProduct denotes endoglin

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T1 23-31 GeneOrGeneProduct denotes endoglin

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T1 54-72 DiseaseOrPhenotypicFeature denotes systemic sclerosis D012595

LitCoin-GeneOrGeneProduct-v3

Id Subject Object Predicate Lexical cue
T1 23-31 GeneOrGeneProduct denotes endoglin

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T1 54-72 DiseaseOrPhenotypicFeature denotes systemic sclerosis 0005100

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T1 54-72 DiseaseOrPhenotypicFeature denotes systemic sclerosis D012595

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T1 54-72 DiseaseOrPhenotypicFeature denotes systemic sclerosis D012595

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label
T3851 23-31 GeneOrGeneProduct denotes endoglin
T94954 54-72 DiseaseOrPhenotypicFeature denotes systemic sclerosis D012595

DisGeNET

Id Subject Object Predicate Lexical cue
T0 23-31 gene:2022 denotes endoglin
T1 54-72 disease:C0036421 denotes systemic sclerosis
T2 23-31 gene:2022 denotes endoglin
T4 23-31 gene:2022 denotes endoglin
T6 23-31 gene:2022 denotes endoglin
R1 T0 T1 associated_with endoglin,systemic sclerosis

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
17166870-0#23#31#gene2022 23-31 gene2022 denotes endoglin
17166870-0#54#72#diseaseC0036421 54-72 diseaseC0036421 denotes systemic sclerosis
23#31#gene202254#72#diseaseC0036421 17166870-0#23#31#gene2022 17166870-0#54#72#diseaseC0036421 associated_with endoglin,systemic sclerosis