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PubMed:20534762 / 444-477 JSONTXT

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LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
7529 0-33 DiseaseOrPhenotypicFeature denotes congenital central hypothyroidism MESH:D003409

LitCoin_Mondo

Id Subject Object Predicate Lexical cue mondo_id
T6 0-10 DiseaseOrPhenotypicFeature denotes congenital 0021140
T7 19-33 DiseaseOrPhenotypicFeature denotes hypothyroidism 0005420

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T3 11-33 DiseaseOrPhenotypicFeature denotes central hypothyroidism D007037

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T3 11-33 DiseaseOrPhenotypicFeature denotes central hypothyroidism 0016410

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T3 11-33 DiseaseOrPhenotypicFeature denotes central hypothyroidism D007037

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T3 11-33 DiseaseOrPhenotypicFeature denotes central hypothyroidism D007037

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label
T62466 11-33 DiseaseOrPhenotypicFeature denotes central hypothyroidism D007037

UBERON-AE

Id Subject Object Predicate Lexical cue
PD-UBERON-AE-B_T2 11-18 http://purl.obolibrary.org/obo/UBERON_0012131 denotes central

PubCasesHPO

Id Subject Object Predicate Lexical cue
AB2 11-33 HP:0011787 denotes central hypothyroidism

performance-test

Id Subject Object Predicate Lexical cue
PD-UBERON-AE-B_T2 11-18 http://purl.obolibrary.org/obo/UBERON_0012131 denotes central