PubMed:15111599 / 1364-1421 JSONTXT

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LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
730 0-57 DiseaseOrPhenotypicFeature denotes autosomal dominant congenital nuclear lactescent cataract MESH:C565137

LitCoin_Mondo

Id Subject Object Predicate Lexical cue mondo_id
T10 19-29 DiseaseOrPhenotypicFeature denotes congenital 0021140
T11 49-57 DiseaseOrPhenotypicFeature denotes cataract 0005129

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T31 49-57 GeneOrGeneProduct denotes cataract

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T13 49-57 GeneOrGeneProduct denotes cataract

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T5 49-57 DiseaseOrPhenotypicFeature denotes cataract D002386

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T6 49-57 DiseaseOrPhenotypicFeature denotes cataract 0005129

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T6 0-57 DiseaseOrPhenotypicFeature denotes autosomal dominant congenital nuclear lactescent cataract DISEASE

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T6 0-57 DiseaseOrPhenotypicFeature denotes autosomal dominant congenital nuclear lactescent cataract DISEASE

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label
T6 0-57 DiseaseOrPhenotypicFeature denotes autosomal dominant congenital nuclear lactescent cataract DISEASE