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PubMed:10079245 JSONTXT

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PMID_GLOBAL

Id Subject Object Predicate Lexical cue mondo_id
T1 70-92 DiseaseOrPhenotypicFeature denotes Peutz-Jeghers syndrome 0008280
T2 135-144 DiseaseOrPhenotypicFeature denotes polyposis 0000147
T3 233-255 DiseaseOrPhenotypicFeature denotes Peutz-Jeghers syndrome 0008280
T4 289-311 DiseaseOrPhenotypicFeature denotes neoplasms of the colon 0005401
T5 339-347 DiseaseOrPhenotypicFeature denotes pancreas 0021040
T6 370-376 DiseaseOrPhenotypicFeature denotes cervix 0021230
T7 430-435 DiseaseOrPhenotypicFeature denotes tumor 0005070
T8 609-614 DiseaseOrPhenotypicFeature denotes tumor 0005070
T9 656-661 DiseaseOrPhenotypicFeature denotes tumor 0005070
T10 709-715 DiseaseOrPhenotypicFeature denotes defect 0008568
T11 729-737 DiseaseOrPhenotypicFeature denotes melanoma 0005105
T12 748-755 DiseaseOrPhenotypicFeature denotes myeloma 0009693
T13 999-1003 DiseaseOrPhenotypicFeature denotes lung 0021117
T14 1008-1012 DiseaseOrPhenotypicFeature denotes soft 0013894
T15 1028-1040 DiseaseOrPhenotypicFeature denotes renal tumors 0021163
T16 1234-1257 DiseaseOrPhenotypicFeature denotes cervical adenocarcinoma 0005153|0016275
T18 1374-1393 DiseaseOrPhenotypicFeature denotes lung adenocarcinoma 0005061
T19 1566-1586 DiseaseOrPhenotypicFeature denotes pancreatic carcinoma 0005192
T20 1756-1761 DiseaseOrPhenotypicFeature denotes tumor 0005070

DisGeNET5_variant_disease

Id Subject Object Predicate Lexical cue
10079245-11#19#25#geners375328708 1543-1549 geners375328708 denotes C1257T
10079245-11#42#62#diseaseC0235974 1566-1586 diseaseC0235974 denotes pancreatic carcinoma
19#25#geners37532870842#62#diseaseC0235974 10079245-11#19#25#geners375328708 10079245-11#42#62#diseaseC0235974 associated_with C1257T,pancreatic carcinoma

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
10079245-1#22#26#gene6794 65-69 gene6794 denotes LKB1
10079245-1#27#49#diseaseC0031269 70-92 diseaseC0031269 denotes Peutz-Jeghers syndrome
10079245-1#78#101#diseaseC0334092 121-144 diseaseC0334092 denotes hamartomatous polyposis
10079245-3#41#45#gene6794 555-559 gene6794 denotes LKB1
10079245-3#64#77#diseaseC0596263 578-591 diseaseC0596263 denotes tumorigenesis
10079245-4#63#67#gene6794 788-792 gene6794 denotes LKB1
10079245-4#4#12#diseaseC0025202 729-737 diseaseC0025202 denotes melanoma
10079245-4#23#30#diseaseC0026764 748-755 diseaseC0026764 denotes myeloma
22#26#gene679427#49#diseaseC0031269 10079245-1#22#26#gene6794 10079245-1#27#49#diseaseC0031269 associated_with LKB1,Peutz-Jeghers syndrome
22#26#gene679478#101#diseaseC0334092 10079245-1#22#26#gene6794 10079245-1#78#101#diseaseC0334092 associated_with LKB1,hamartomatous polyposis
41#45#gene679464#77#diseaseC0596263 10079245-3#41#45#gene6794 10079245-3#64#77#diseaseC0596263 associated_with LKB1,tumorigenesis
63#67#gene67944#12#diseaseC0025202 10079245-4#63#67#gene6794 10079245-4#4#12#diseaseC0025202 associated_with LKB1,melanoma
63#67#gene679423#30#diseaseC0026764 10079245-4#63#67#gene6794 10079245-4#23#30#diseaseC0026764 associated_with LKB1,myeloma

DisGeNET

Id Subject Object Predicate Lexical cue
T0 555-559 gene:6794 denotes LKB1
T1 578-591 disease:C0596263 denotes tumorigenesis
T2 555-559 gene:6794 denotes LKB1
T3 687-694 disease:C0006826 denotes cancers
T4 719-723 gene:6794 denotes LKB1
T5 687-694 disease:C0006826 denotes cancers
R1 T0 T1 associated_with LKB1,tumorigenesis
R2 T2 T3 associated_with LKB1,cancers
R3 T4 T5 associated_with LKB1,cancers

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 121-144 HP_0004390 denotes hamartomatous polyposis
T2 121-134 HP_0010566 denotes hamartomatous
T3 152-195 HP_0007378 denotes gastrointestinal tract as well as to cancer
T4 189-195 HP_0002664 denotes cancer
T5 289-298 HP_0002664 denotes neoplasms
T6 289-311 HP_0003003 denotes neoplasms of the colon
T7 289-311 HP_0100273 denotes neoplasms of the colon
T8 378-395 HP_0001428 denotes somatic mutations
T9 430-435 HP_0002664 denotes tumor
T10 497-511 HP_0003002 denotes breast cancers
T11 497-511 HP_0100013 denotes breast cancers
T12 504-511 HP_0002664 denotes cancers
T13 534-551 HP_0001428 denotes somatic mutations
T14 609-614 HP_0002664 denotes tumor
T15 656-661 HP_0002664 denotes tumor
T16 687-694 HP_0002664 denotes cancers
T17 729-737 HP_0002861 denotes melanoma
T18 793-810 HP_0001428 denotes somatic mutations
T19 1028-1040 HP_0009726 denotes renal tumors
T20 1034-1040 HP_0002664 denotes tumors
T21 1374-1393 HP_0030078 denotes lung adenocarcinoma
T22 1756-1761 HP_0002664 denotes tumor