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PubMed:10204851 JSONTXT

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PMID_GLOBAL

Id Subject Object Predicate Lexical cue mondo_id
T1 85-108 DiseaseOrPhenotypicFeature denotes hereditary pancreatitis 0008185
T2 110-133 DiseaseOrPhenotypicFeature denotes Hereditary pancreatitis 0008185
T3 135-137 DiseaseOrPhenotypicFeature denotes HP 0006249|0017853|0008185
T6 208-220 DiseaseOrPhenotypicFeature denotes pancreatitis 0004982
T7 402-425 DiseaseOrPhenotypicFeature denotes hereditary pancreatitis 0008185
T8 629-631 DiseaseOrPhenotypicFeature denotes HP 0006249|0017853|0008185
T11 706-729 DiseaseOrPhenotypicFeature denotes hereditary pancreatitis 0008185
T12 762-764 DiseaseOrPhenotypicFeature denotes HP 0006249|0017853|0008185
T15 1405-1407 DiseaseOrPhenotypicFeature denotes HP 0006249|0017853|0008185
T18 1520-1522 DiseaseOrPhenotypicFeature denotes HP 0006249|0017853|0008185
T21 1588-1603 DiseaseOrPhenotypicFeature denotes genetic disease 0003847

DisGeNET5_variant_disease

Id Subject Object Predicate Lexical cue
10204851-3#156#205#geners146966861 502-551 geners146966861 denotes arginine to histidine substitution at residue 117
10204851-3#56#79#diseaseC0238339 402-425 diseaseC0238339 denotes hereditary pancreatitis
10204851-3#283#285#diseaseC0238339 629-631 diseaseC0238339 denotes HP
156#205#geners14696686156#79#diseaseC0238339 10204851-3#156#205#geners146966861 10204851-3#56#79#diseaseC0238339 associated_with arginine to histidine substitution at residue 117,hereditary pancreatitis
156#205#geners146966861283#285#diseaseC0238339 10204851-3#156#205#geners146966861 10204851-3#283#285#diseaseC0238339 associated_with arginine to histidine substitution at residue 117,HP

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
10204851-0#17#37#gene5644 17-37 gene5644 denotes cationic trypsinogen
10204851-0#85#108#diseaseC0238339 85-108 diseaseC0238339 denotes hereditary pancreatitis
10204851-3#240#244#gene5646 586-590 gene5646 denotes try4
10204851-3#56#79#diseaseC0238339 402-425 diseaseC0238339 denotes hereditary pancreatitis
10204851-3#283#285#diseaseC0238339 629-631 diseaseC0238339 denotes HP
17#37#gene564485#108#diseaseC0238339 10204851-0#17#37#gene5644 10204851-0#85#108#diseaseC0238339 associated_with cationic trypsinogen,hereditary pancreatitis
240#244#gene564656#79#diseaseC0238339 10204851-3#240#244#gene5646 10204851-3#56#79#diseaseC0238339 associated_with try4,hereditary pancreatitis
240#244#gene5646283#285#diseaseC0238339 10204851-3#240#244#gene5646 10204851-3#283#285#diseaseC0238339 associated_with try4,HP

DisGeNET

Id Subject Object Predicate Lexical cue
T0 1376-1396 gene:5644 denotes cationic trypsinogen
T1 1405-1407 disease:C0238339 denotes HP
R1 T0 T1 associated_with cationic trypsinogen,HP

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 293-317 HP_0000006 denotes autosomal dominant trait
T2 293-311 HP_0000006 denotes autosomal dominant