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PubMed:15111599 / 55-101 JSONTXT

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LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
719 0-46 DiseaseOrPhenotypicFeature denotes autosomal dominant congenital nuclear cataract MESH:C565137

LitCoin_Mondo

Id Subject Object Predicate Lexical cue mondo_id
T1 19-29 DiseaseOrPhenotypicFeature denotes congenital 0021140
T2 30-46 DiseaseOrPhenotypicFeature denotes nuclear cataract 0045050
T3 38-46 DiseaseOrPhenotypicFeature denotes cataract 0005129

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T4 38-46 GeneOrGeneProduct denotes cataract

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T2 38-46 GeneOrGeneProduct denotes cataract

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T1 38-46 DiseaseOrPhenotypicFeature denotes cataract D002386

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T1 30-46 DiseaseOrPhenotypicFeature denotes nuclear cataract 0045050

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T1 0-46 DiseaseOrPhenotypicFeature denotes autosomal dominant congenital nuclear cataract DISEASE

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T1 0-46 DiseaseOrPhenotypicFeature denotes autosomal dominant congenital nuclear cataract DISEASE

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label
T74043 0-46 DiseaseOrPhenotypicFeature denotes autosomal dominant congenital nuclear cataract DISEASE