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PubMed:19381301 JSONTXT

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DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
19381301-8#3#6#gene1536 854-857 gene1536 denotes CGD
19381301-8#127#130#gene1536 978-981 gene1536 denotes CGD
19381301-8#91#93#diseaseC0003504 942-944 diseaseC0003504 denotes AR
19381301-8#183#185#diseaseC0003504 1034-1036 diseaseC0003504 denotes AR
19381301-8#91#93#diseaseC0003504 942-944 diseaseC0003504 denotes AR
3#6#gene153691#93#diseaseC0003504 19381301-8#3#6#gene1536 19381301-8#91#93#diseaseC0003504 associated_with CGD,AR
3#6#gene1536183#185#diseaseC0003504 19381301-8#3#6#gene1536 19381301-8#183#185#diseaseC0003504 associated_with CGD,AR
3#6#gene153691#93#diseaseC0003504 19381301-8#3#6#gene1536 19381301-8#91#93#diseaseC0003504 associated_with CGD,AR
127#130#gene153691#93#diseaseC0003504 19381301-8#127#130#gene1536 19381301-8#91#93#diseaseC0003504 associated_with CGD,AR
127#130#gene1536183#185#diseaseC0003504 19381301-8#127#130#gene1536 19381301-8#183#185#diseaseC0003504 associated_with CGD,AR
127#130#gene153691#93#diseaseC0003504 19381301-8#127#130#gene1536 19381301-8#91#93#diseaseC0003504 associated_with CGD,AR

PMID_GLOBAL

Id Subject Object Predicate Lexical cue mondo_id
T1 0-29 DiseaseOrPhenotypicFeature denotes Chronic granulomatous disease 0018305
T2 56-59 DiseaseOrPhenotypicFeature denotes CGD 0010600|0018305
T4 66-82 DiseaseOrPhenotypicFeature denotes immunodeficiency 0021094
T5 369-372 DiseaseOrPhenotypicFeature denotes CGD 0010600|0018305
T7 522-525 DiseaseOrPhenotypicFeature denotes CGD 0010600|0018305
T9 746-749 DiseaseOrPhenotypicFeature denotes CGD 0010600|0018305
T11 854-857 DiseaseOrPhenotypicFeature denotes CGD 0010600|0018305
T13 978-981 DiseaseOrPhenotypicFeature denotes CGD 0010600|0018305
T15 1125-1129 DiseaseOrPhenotypicFeature denotes skin 0002531
T16 1749-1758 DiseaseOrPhenotypicFeature denotes pneumonia 0005249
T17 1773-1780 DiseaseOrPhenotypicFeature denotes abscess 0005227
T18 1825-1832 DiseaseOrPhenotypicFeature denotes abscess 0005227
T19 1902-1905 DiseaseOrPhenotypicFeature denotes CGD 0010600|0018305
T21 1930-1933 DiseaseOrPhenotypicFeature denotes can 0012833