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PubMed:17166870 / 0-207 JSONTXT

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LitCoin-sentences

Id Subject Object Predicate Lexical cue
T1 0-113 Sentence denotes Association between an endoglin gene polymorphism and systemic sclerosis-related pulmonary arterial hypertension.
T2 114-125 Sentence denotes UNLABELLED:

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
3695 81-112 DiseaseOrPhenotypicFeature denotes pulmonary arterial hypertension MESH:D000081029
3696 126-144 DiseaseOrPhenotypicFeature denotes Systemic sclerosis MESH:D012595
3697 146-149 DiseaseOrPhenotypicFeature denotes SSc MESH:D012595

LitCoin_Mondo

Id Subject Object Predicate Lexical cue mondo_id
T1 54-72 DiseaseOrPhenotypicFeature denotes systemic sclerosis 0005100
T2 81-112 DiseaseOrPhenotypicFeature denotes pulmonary arterial hypertension 0015924
T3 126-144 DiseaseOrPhenotypicFeature denotes Systemic sclerosis 0005100

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T1 23-31 GeneOrGeneProduct denotes endoglin
T2 100-112 GeneOrGeneProduct denotes hypertension
T3 200-205 GeneOrGeneProduct denotes early

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T1 23-31 GeneOrGeneProduct denotes endoglin
T2 100-112 GeneOrGeneProduct denotes hypertension
T3 145-155 GeneOrGeneProduct denotes (SSc) is a
T4 200-205 GeneOrGeneProduct denotes early

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T1 54-72 DiseaseOrPhenotypicFeature denotes systemic sclerosis D012595
T2 81-112 DiseaseOrPhenotypicFeature denotes pulmonary arterial hypertension D000081029
T3 126-144 DiseaseOrPhenotypicFeature denotes Systemic sclerosis D012595
T4 146-149 DiseaseOrPhenotypicFeature denotes SSc 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
T2 81-112 DiseaseOrPhenotypicFeature denotes pulmonary arterial hypertension 0024533|0015924
T4 126-144 DiseaseOrPhenotypicFeature denotes Systemic sclerosis 0005100
T5 146-149 DiseaseOrPhenotypicFeature denotes SSc 0005100
T6 156-182 DiseaseOrPhenotypicFeature denotes connective tissue disorder 0003900

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T1 54-72 DiseaseOrPhenotypicFeature denotes systemic sclerosis D012595
T2 81-112 DiseaseOrPhenotypicFeature denotes pulmonary arterial hypertension D000081029
T3 126-144 DiseaseOrPhenotypicFeature denotes Systemic sclerosis D012595
T4 146-149 DiseaseOrPhenotypicFeature denotes SSc D012595

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T1 54-72 DiseaseOrPhenotypicFeature denotes systemic sclerosis D012595
T2 81-112 DiseaseOrPhenotypicFeature denotes pulmonary arterial hypertension D000081029
T3 126-144 DiseaseOrPhenotypicFeature denotes Systemic sclerosis D012595
T4 146-149 DiseaseOrPhenotypicFeature denotes SSc D012595

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label
T3851 23-31 GeneOrGeneProduct denotes endoglin
T65914 146-149 DiseaseOrPhenotypicFeature denotes SSc D012595
T88367 126-144 DiseaseOrPhenotypicFeature denotes Systemic sclerosis D012595
T96334 81-112 DiseaseOrPhenotypicFeature denotes pulmonary arterial hypertension D000081029
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
T3 81-112 disease:C0152171 denotes pulmonary arterial hypertension
T4 23-31 gene:2022 denotes endoglin
T5 81-112 disease:C2973725 denotes pulmonary arterial hypertension
T6 23-31 gene:2022 denotes endoglin
T7 81-112 disease:C3714844 denotes pulmonary arterial hypertension
R1 T0 T1 associated_with endoglin,systemic sclerosis
R2 T2 T3 associated_with endoglin,pulmonary arterial hypertension
R3 T4 T5 associated_with endoglin,pulmonary arterial hypertension
R4 T6 T7 associated_with endoglin,pulmonary arterial hypertension

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 156-182 HP_0003549 denotes connective tissue disorder

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
17166870-0#81#112#diseaseC3203102 81-112 diseaseC3203102 denotes pulmonary arterial hypertension
23#31#gene202254#72#diseaseC0036421 17166870-0#23#31#gene2022 17166870-0#54#72#diseaseC0036421 associated_with endoglin,systemic sclerosis
23#31#gene202281#112#diseaseC3203102 17166870-0#23#31#gene2022 17166870-0#81#112#diseaseC3203102 associated_with endoglin,pulmonary arterial hypertension