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PubMed:20534762 / 186-211 JSONTXT

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LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
7525 0-25 DiseaseOrPhenotypicFeature denotes congenital hypothyroidism MESH:D003409

LitCoin_Mondo

Id Subject Object Predicate Lexical cue mondo_id
T3 0-25 DiseaseOrPhenotypicFeature denotes congenital hypothyroidism 0018612
T4 0-10 DiseaseOrPhenotypicFeature denotes congenital 0021140
T5 11-25 DiseaseOrPhenotypicFeature denotes hypothyroidism 0005420

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T2 0-25 DiseaseOrPhenotypicFeature denotes congenital hypothyroidism D003409

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T2 0-25 DiseaseOrPhenotypicFeature denotes congenital hypothyroidism 0018612

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T2 0-25 DiseaseOrPhenotypicFeature denotes congenital hypothyroidism D003409

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T2 0-25 DiseaseOrPhenotypicFeature denotes congenital hypothyroidism D003409

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label
T3451 0-25 DiseaseOrPhenotypicFeature denotes congenital hypothyroidism D003409

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 0-25 HP_0000851 denotes congenital hypothyroidism
T2 11-25 HP_0000821 denotes hypothyroidism

PubCasesHPO

Id Subject Object Predicate Lexical cue
AB1 0-25 HP:0000851 denotes congenital hypothyroidism