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PubMed:15033202 / 835-968 JSONTXT

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LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
591 19-27 OrganismTaxon denotes patients NCBITaxon:9606
592 123-127 GeneOrGeneProduct denotes NBS1 NCBIGene:4683

LitCoin-sentences

Id Subject Object Predicate Lexical cue
T7 0-133 Sentence denotes We tested 67 Czech patients of different ages with simple microcephaly for the presence of the most common mutation in the NBS1 gene.

LitCoin_Mondo

Id Subject Object Predicate Lexical cue mondo_id
T12 58-70 DiseaseOrPhenotypicFeature denotes microcephaly 0001149

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T20 3-9 GeneOrGeneProduct denotes tested
T21 51-57 GeneOrGeneProduct denotes simple
T22 107-115 GeneOrGeneProduct denotes mutation
T23 123-127 GeneOrGeneProduct denotes NBS1

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T16 123-127 GeneOrGeneProduct denotes NBS1

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T13 58-70 DiseaseOrPhenotypicFeature denotes microcephaly D008831

LitCoin-GeneOrGeneProduct-v3

Id Subject Object Predicate Lexical cue
T7 123-127 GeneOrGeneProduct denotes NBS1

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T12 58-70 DiseaseOrPhenotypicFeature denotes microcephaly 0001149

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T15 58-70 DiseaseOrPhenotypicFeature denotes microcephaly D008831

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T14 58-70 DiseaseOrPhenotypicFeature denotes microcephaly D008831

LitCoin-NCBITaxon-2

Id Subject Object Predicate Lexical cue
T3 19-27 OrganismTaxon denotes patients

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label
T7 123-127 GeneOrGeneProduct denotes NBS1
T16923 58-70 DiseaseOrPhenotypicFeature denotes microcephaly D008831
T18419 19-27 OrganismTaxon denotes patients

DisGeNET

Id Subject Object Predicate Lexical cue
T0 123-127 gene:4683 denotes NBS1
T1 58-70 disease:C0025958 denotes microcephaly
T2 123-127 gene:55655 denotes NBS1
T3 58-70 disease:C0025958 denotes microcephaly
R1 T0 T1 associated_with NBS1,microcephaly
R2 T2 T3 associated_with NBS1,microcephaly