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PubMed:17033686 / 444-484 JSONTXT

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LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
3456 0-40 DiseaseOrPhenotypicFeature denotes X-linked phenotype of mental retardation MESH:D038901

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T15 0-8 GeneOrGeneProduct denotes X-linked

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T9 0-8 GeneOrGeneProduct denotes X-linked

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T7 22-40 DiseaseOrPhenotypicFeature denotes mental retardation D008607

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T8 22-40 DiseaseOrPhenotypicFeature denotes mental retardation 0001071

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T9 0-40 DiseaseOrPhenotypicFeature denotes X-linked phenotype of mental retardation DISEASE

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T9 0-40 DiseaseOrPhenotypicFeature denotes X-linked phenotype of mental retardation DISEASE

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label
T96765 0-40 DiseaseOrPhenotypicFeature denotes X-linked phenotype of mental retardation DISEASE

PubmedHPO

Id Subject Object Predicate Lexical cue
T3 0-8 HP_0001417 denotes X-linked
T4 22-40 HP_0001249 denotes mental retardation