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PubMed:15033202 / 639-738 JSONTXT

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LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
589 17-43 DiseaseOrPhenotypicFeature denotes Nijmegen breakage syndrome MESH:D049932
590 64-84 DiseaseOrPhenotypicFeature denotes primary microcephaly MESH:D008831

LitCoin-sentences

Id Subject Object Predicate Lexical cue
T5 0-99 Sentence denotes The frequency of Nijmegen breakage syndrome among children with primary microcephaly was not known.

LitCoin_Mondo

Id Subject Object Predicate Lexical cue mondo_id
T10 17-43 DiseaseOrPhenotypicFeature denotes Nijmegen breakage syndrome 0009623
T11 72-84 DiseaseOrPhenotypicFeature denotes microcephaly 0001149

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T15 4-13 GeneOrGeneProduct denotes frequency
T16 35-43 GeneOrGeneProduct denotes syndrome

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T12 4-13 GeneOrGeneProduct denotes frequency
T13 35-43 GeneOrGeneProduct denotes syndrome

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T10 17-43 DiseaseOrPhenotypicFeature denotes Nijmegen breakage syndrome D049932
T11 72-84 DiseaseOrPhenotypicFeature denotes microcephaly D008831

LitCoin-GeneOrGeneProduct-v3

Id Subject Object Predicate Lexical cue
T6 17-43 GeneOrGeneProduct denotes Nijmegen breakage syndrome

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T9 17-43 DiseaseOrPhenotypicFeature denotes Nijmegen breakage syndrome 0009623
T10 64-84 DiseaseOrPhenotypicFeature denotes primary microcephaly 0016056

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T12 17-43 DiseaseOrPhenotypicFeature denotes Nijmegen breakage syndrome D049932
T13 72-84 DiseaseOrPhenotypicFeature denotes microcephaly D008831

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T12 17-43 DiseaseOrPhenotypicFeature denotes Nijmegen breakage syndrome D049932
T13 72-84 DiseaseOrPhenotypicFeature denotes microcephaly D008831

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label
T6 17-43 GeneOrGeneProduct denotes Nijmegen breakage syndrome
T82266 72-84 DiseaseOrPhenotypicFeature denotes microcephaly D008831
T24765 17-43 DiseaseOrPhenotypicFeature denotes Nijmegen breakage syndrome D049932