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PubMed:15754732 / 0-217 JSONTXT

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LitCoin-sentences

Id Subject Object Predicate Lexical cue
T1 0-122 Sentence denotes Novel somatic MEN1 gene alterations in sporadic primary hyperparathyroidism and correlation with clinical characteristics.

LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
1545 14-18 GeneOrGeneProduct denotes MEN1 NCBIGene:4221
1546 48-75 DiseaseOrPhenotypicFeature denotes primary hyperparathyroidism MESH:D049950
1547 123-150 DiseaseOrPhenotypicFeature denotes Primary hyperparathyroidism MESH:D049950
1548 152-156 DiseaseOrPhenotypicFeature denotes pHPT MESH:D049950
1549 170-187 DiseaseOrPhenotypicFeature denotes endocrine disease MESH:D004700

LitCoin_Mondo

Id Subject Object Predicate Lexical cue mondo_id
T1 48-75 DiseaseOrPhenotypicFeature denotes primary hyperparathyroidism 0010837
T2 56-75 DiseaseOrPhenotypicFeature denotes hyperparathyroidism 0001741
T3 123-150 DiseaseOrPhenotypicFeature denotes Primary hyperparathyroidism 0010837
T4 131-150 DiseaseOrPhenotypicFeature denotes hyperparathyroidism 0001741

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T1 0-5 GeneOrGeneProduct denotes Novel
T2 14-18 GeneOrGeneProduct denotes MEN1

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T1 0-5 GeneOrGeneProduct denotes Novel
T2 14-18 GeneOrGeneProduct denotes MEN1

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T1 48-75 DiseaseOrPhenotypicFeature denotes primary hyperparathyroidism D049950
T2 123-150 DiseaseOrPhenotypicFeature denotes Primary hyperparathyroidism D049950
T3 152-156 DiseaseOrPhenotypicFeature denotes pHPT D049950
T4 170-187 DiseaseOrPhenotypicFeature denotes endocrine disease D004700

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T1 14-18 DiseaseOrPhenotypicFeature denotes MEN1 0007540
T2 48-75 DiseaseOrPhenotypicFeature denotes primary hyperparathyroidism 0010837
T3 123-150 DiseaseOrPhenotypicFeature denotes Primary hyperparathyroidism 0010837
T4 152-156 DiseaseOrPhenotypicFeature denotes pHPT 0010837
T5 170-187 DiseaseOrPhenotypicFeature denotes endocrine disease 0005151

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T1 14-18 DiseaseOrPhenotypicFeature denotes MEN1 DISEASE
T2 48-75 DiseaseOrPhenotypicFeature denotes primary hyperparathyroidism D049950
T3 123-150 DiseaseOrPhenotypicFeature denotes Primary hyperparathyroidism D049950
T4 152-156 DiseaseOrPhenotypicFeature denotes pHPT D049950
T5 170-187 DiseaseOrPhenotypicFeature denotes endocrine disease D004700

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T1 48-75 DiseaseOrPhenotypicFeature denotes primary hyperparathyroidism D049950
T2 123-150 DiseaseOrPhenotypicFeature denotes Primary hyperparathyroidism D049950
T3 152-156 DiseaseOrPhenotypicFeature denotes pHPT D049950
T4 170-187 DiseaseOrPhenotypicFeature denotes endocrine disease D004700

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label
T4 170-187 DiseaseOrPhenotypicFeature denotes endocrine disease D004700
T95728 152-156 DiseaseOrPhenotypicFeature denotes pHPT D049950
T2 123-150 DiseaseOrPhenotypicFeature denotes Primary hyperparathyroidism D049950
T38477 48-75 DiseaseOrPhenotypicFeature denotes primary hyperparathyroidism D049950

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
15754732-0#14#18#gene4221 14-18 gene4221 denotes MEN1
15754732-0#48#75#diseaseC0221002 48-75 diseaseC0221002 denotes primary hyperparathyroidism
14#18#gene422148#75#diseaseC0221002 15754732-0#14#18#gene4221 15754732-0#48#75#diseaseC0221002 associated_with MEN1,primary hyperparathyroidism

DisGeNET

Id Subject Object Predicate Lexical cue
T0 14-18 gene:4221 denotes MEN1
T1 48-75 disease:C0221002 denotes primary hyperparathyroidism
T3 152-156 disease:C0221002 denotes pHPT
T5 123-150 disease:C0221002 denotes Primary hyperparathyroidism
T7 170-187 disease:C0014130 denotes endocrine disease
R1 T0 T1 associated_with MEN1,primary hyperparathyroidism