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PubMed:10390531 JSONTXT

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PubmedHPO

Id Subject Object Predicate Lexical cue
T1 273-288 HP_0000992 denotes sun sensitivity
T2 311-322 HP_0008069 denotes skin cancer
T3 316-322 HP_0002664 denotes cancer

DisGeNET

Id Subject Object Predicate Lexical cue
T0 1003-1022 gene:100 denotes adenosine deaminase
T1 933-935 disease:C0043346 denotes XP
T2 1003-1022 gene:100 denotes adenosine deaminase
T3 942-944 disease:C0043346 denotes XP
R1 T0 T1 associated_with adenosine deaminase,XP
R2 T2 T3 associated_with adenosine deaminase,XP

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
10390531-5#102#121#gene100 1003-1022 gene100 denotes adenosine deaminase
10390531-5#46#48#diseaseC0009207 947-949 diseaseC0009207 denotes CS
102#121#gene10046#48#diseaseC0009207 10390531-5#102#121#gene100 10390531-5#46#48#diseaseC0009207 associated_with adenosine deaminase,CS

PMID_GLOBAL

Id Subject Object Predicate Lexical cue mondo_id
T1 11-15 DiseaseOrPhenotypicFeature denotes XP-D 0010212
T2 11-13 DiseaseOrPhenotypicFeature denotes XP 0019600
T3 20-24 DiseaseOrPhenotypicFeature denotes XP-D 0010212
T4 20-22 DiseaseOrPhenotypicFeature denotes XP 0019600
T5 25-27 DiseaseOrPhenotypicFeature denotes CS 0008021|0016006
T7 176-197 DiseaseOrPhenotypicFeature denotes Xeroderma pigmentosum 0019600
T8 199-201 DiseaseOrPhenotypicFeature denotes XP 0019600
T9 277-288 DiseaseOrPhenotypicFeature denotes sensitivity 0000605
T10 311-322 DiseaseOrPhenotypicFeature denotes skin cancer 0002898
T11 329-331 DiseaseOrPhenotypicFeature denotes XP 0019600
T12 379-396 DiseaseOrPhenotypicFeature denotes Cockayne syndrome 0016006
T13 398-400 DiseaseOrPhenotypicFeature denotes CS 0008021|0016006
T15 529-531 DiseaseOrPhenotypicFeature denotes XP 0019600
T16 555-578 DiseaseOrPhenotypicFeature denotes complementation group D 0008840
T17 623-625 DiseaseOrPhenotypicFeature denotes CS 0008021|0016006
T19 646-655 DiseaseOrPhenotypicFeature denotes sensitive 0000605
T20 719-723 DiseaseOrPhenotypicFeature denotes XP-D 0010212
T21 719-721 DiseaseOrPhenotypicFeature denotes XP 0019600
T22 759-770 DiseaseOrPhenotypicFeature denotes sensitivity 0000605
T23 793-797 DiseaseOrPhenotypicFeature denotes XP-D 0010212
T24 793-795 DiseaseOrPhenotypicFeature denotes XP 0019600
T25 798-800 DiseaseOrPhenotypicFeature denotes CS 0008021|0016006
T27 814-820 DiseaseOrPhenotypicFeature denotes defect 0008568
T28 933-937 DiseaseOrPhenotypicFeature denotes XP-D 0010212
T29 933-935 DiseaseOrPhenotypicFeature denotes XP 0019600
T30 942-946 DiseaseOrPhenotypicFeature denotes XP-D 0010212
T31 942-944 DiseaseOrPhenotypicFeature denotes XP 0019600
T32 947-949 DiseaseOrPhenotypicFeature denotes CS 0008021|0016006
T34 1029-1032 DiseaseOrPhenotypicFeature denotes ADA 0007064
T35 1279-1283 DiseaseOrPhenotypicFeature denotes XP-D 0010212
T36 1279-1281 DiseaseOrPhenotypicFeature denotes XP 0019600
T37 1288-1292 DiseaseOrPhenotypicFeature denotes XP-D 0010212
T38 1288-1290 DiseaseOrPhenotypicFeature denotes XP 0019600
T39 1293-1295 DiseaseOrPhenotypicFeature denotes CS 0008021|0016006
T41 1408-1411 DiseaseOrPhenotypicFeature denotes ADA 0007064
T42 1474-1478 DiseaseOrPhenotypicFeature denotes XP-D 0010212
T43 1474-1476 DiseaseOrPhenotypicFeature denotes XP 0019600
T44 1577-1581 DiseaseOrPhenotypicFeature denotes XP-D 0010212
T45 1577-1579 DiseaseOrPhenotypicFeature denotes XP 0019600
T46 1582-1584 DiseaseOrPhenotypicFeature denotes CS 0008021|0016006
T48 1804-1808 DiseaseOrPhenotypicFeature denotes XP-D 0010212
T49 1804-1806 DiseaseOrPhenotypicFeature denotes XP 0019600
T50 1813-1817 DiseaseOrPhenotypicFeature denotes XP-D 0010212
T51 1813-1815 DiseaseOrPhenotypicFeature denotes XP 0019600
T52 1818-1820 DiseaseOrPhenotypicFeature denotes CS 0008021|0016006
T54 1859-1870 DiseaseOrPhenotypicFeature denotes sensitivity 0000605
T55 1874-1878 DiseaseOrPhenotypicFeature denotes XP-D 0010212
T56 1874-1876 DiseaseOrPhenotypicFeature denotes XP 0019600
T57 1879-1881 DiseaseOrPhenotypicFeature denotes CS 0008021|0016006
T59 1910-1921 DiseaseOrPhenotypicFeature denotes sensitivity 0000605
T60 1925-1929 DiseaseOrPhenotypicFeature denotes XP-D 0010212
T61 1925-1927 DiseaseOrPhenotypicFeature denotes XP 0019600
T62 1930-1932 DiseaseOrPhenotypicFeature denotes CS 0008021|0016006
T64 1964-1970 DiseaseOrPhenotypicFeature denotes defect 0008568
T65 2026-2032 DiseaseOrPhenotypicFeature denotes defect 0008568