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PubMed:15033202 / 91-354 JSONTXT

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LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
576 4-30 DiseaseOrPhenotypicFeature denotes Nijmegen breakage syndrome MESH:D049932
577 41-93 DiseaseOrPhenotypicFeature denotes autosomal recessive chromosomal instability disorder MESH:D043171
578 117-135 DiseaseOrPhenotypicFeature denotes growth retardation MESH:D006130
579 137-160 DiseaseOrPhenotypicFeature denotes congenital microcephaly MESH:D008831
580 162-178 DiseaseOrPhenotypicFeature denotes immunodeficiency MESH:D007153
581 234-262 DiseaseOrPhenotypicFeature denotes lymphoreticular malignancies MESH:D049932

LitCoin-sentences

Id Subject Object Predicate Lexical cue
T2 0-263 Sentence denotes The Nijmegen breakage syndrome is a rare autosomal recessive chromosomal instability disorder characterized by early growth retardation, congenital microcephaly, immunodeficiency, borderline mental development, and a high tendency to lymphoreticular malignancies.

LitCoin_Mondo

Id Subject Object Predicate Lexical cue mondo_id
T3 4-30 DiseaseOrPhenotypicFeature denotes Nijmegen breakage syndrome 0009623
T4 36-40 DiseaseOrPhenotypicFeature denotes rare 0021136
T5 137-147 DiseaseOrPhenotypicFeature denotes congenital 0021140
T6 148-160 DiseaseOrPhenotypicFeature denotes microcephaly 0001149

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T2 22-30 GeneOrGeneProduct denotes syndrome
T3 36-40 GeneOrGeneProduct denotes rare
T4 111-116 GeneOrGeneProduct denotes early
T5 117-123 GeneOrGeneProduct denotes growth
T6 162-178 GeneOrGeneProduct denotes immunodeficiency
T7 217-221 GeneOrGeneProduct denotes high

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T2 22-30 GeneOrGeneProduct denotes syndrome
T3 36-40 GeneOrGeneProduct denotes rare
T4 111-116 GeneOrGeneProduct denotes early
T5 117-123 GeneOrGeneProduct denotes growth
T6 162-178 GeneOrGeneProduct denotes immunodeficiency
T7 217-221 GeneOrGeneProduct denotes high

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T3 4-30 DiseaseOrPhenotypicFeature denotes Nijmegen breakage syndrome D049932
T4 61-84 DiseaseOrPhenotypicFeature denotes chromosomal instability D043171
T5 148-160 DiseaseOrPhenotypicFeature denotes microcephaly D008831
T6 250-262 DiseaseOrPhenotypicFeature denotes malignancies D009369

LitCoin-GeneOrGeneProduct-v3

Id Subject Object Predicate Lexical cue
T2 4-30 GeneOrGeneProduct denotes Nijmegen breakage syndrome

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T3 4-30 DiseaseOrPhenotypicFeature denotes Nijmegen breakage syndrome 0009623
T4 148-160 DiseaseOrPhenotypicFeature denotes microcephaly 0001149
T5 162-178 DiseaseOrPhenotypicFeature denotes immunodeficiency 0021094

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T3 4-30 DiseaseOrPhenotypicFeature denotes Nijmegen breakage syndrome D049932
T4 61-84 DiseaseOrPhenotypicFeature denotes chromosomal instability D043171
T5 117-135 DiseaseOrPhenotypicFeature denotes growth retardation DISEASE
T6 148-160 DiseaseOrPhenotypicFeature denotes microcephaly D008831
T7 162-178 DiseaseOrPhenotypicFeature denotes immunodeficiency DISEASE
T8 250-262 DiseaseOrPhenotypicFeature denotes malignancies D009369

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T3 4-30 DiseaseOrPhenotypicFeature denotes Nijmegen breakage syndrome D049932
T4 61-84 DiseaseOrPhenotypicFeature denotes chromosomal instability D043171
T5 117-135 DiseaseOrPhenotypicFeature denotes growth retardation DISEASE
T6 148-160 DiseaseOrPhenotypicFeature denotes microcephaly D008831
T7 162-178 DiseaseOrPhenotypicFeature denotes immunodeficiency DISEASE
T8 250-262 DiseaseOrPhenotypicFeature denotes malignancies D009369

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label
T2 4-30 GeneOrGeneProduct denotes Nijmegen breakage syndrome
T13360 250-262 DiseaseOrPhenotypicFeature denotes malignancies D009369
T23922 162-178 DiseaseOrPhenotypicFeature denotes immunodeficiency DISEASE
T84434 148-160 DiseaseOrPhenotypicFeature denotes microcephaly D008831
T925 117-135 DiseaseOrPhenotypicFeature denotes growth retardation DISEASE
T2738 61-84 DiseaseOrPhenotypicFeature denotes chromosomal instability D043171
T83827 4-30 DiseaseOrPhenotypicFeature denotes Nijmegen breakage syndrome D049932