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PubMed:15033202 / 0-115 JSONTXT

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LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
574 0-26 DiseaseOrPhenotypicFeature denotes Nijmegen breakage syndrome MESH:D049932
575 69-89 DiseaseOrPhenotypicFeature denotes primary microcephaly MESH:D008831

LitCoin-sentences

Id Subject Object Predicate Lexical cue
T1 0-90 Sentence denotes Nijmegen breakage syndrome in 13% of age-matched Czech children with primary microcephaly.

LitCoin_Mondo

Id Subject Object Predicate Lexical cue mondo_id
T1 0-26 DiseaseOrPhenotypicFeature denotes Nijmegen breakage syndrome 0009623
T2 77-89 DiseaseOrPhenotypicFeature denotes microcephaly 0001149

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T1 18-26 GeneOrGeneProduct denotes syndrome

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T1 18-26 GeneOrGeneProduct denotes syndrome

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T1 0-26 DiseaseOrPhenotypicFeature denotes Nijmegen breakage syndrome D049932
T2 77-89 DiseaseOrPhenotypicFeature denotes microcephaly D008831

LitCoin-GeneOrGeneProduct-v3

Id Subject Object Predicate Lexical cue
T1 0-26 GeneOrGeneProduct denotes Nijmegen breakage syndrome

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T1 0-26 DiseaseOrPhenotypicFeature denotes Nijmegen breakage syndrome 0009623
T2 69-89 DiseaseOrPhenotypicFeature denotes primary microcephaly 0016056

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T1 0-26 DiseaseOrPhenotypicFeature denotes Nijmegen breakage syndrome D049932
T2 77-89 DiseaseOrPhenotypicFeature denotes microcephaly D008831

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T1 0-26 DiseaseOrPhenotypicFeature denotes Nijmegen breakage syndrome D049932
T2 77-89 DiseaseOrPhenotypicFeature denotes microcephaly D008831

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label
T1 0-26 GeneOrGeneProduct denotes Nijmegen breakage syndrome
T90390 77-89 DiseaseOrPhenotypicFeature denotes microcephaly D008831
T57375 0-26 DiseaseOrPhenotypicFeature denotes Nijmegen breakage syndrome D049932