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LitCoin-sentences

Id Subject Object Predicate Lexical cue
T1 0-158 Sentence denotes Analysis of skin cancer risk factors in immunosuppressed renal transplant patients shows high levels of UV-specific tandem CC to TT mutations of the p53 gene.
T2 159-311 Sentence denotes Immunosuppressed renal transplant recipients (RTRs) are predisposed to non-melanoma skin cancers (NMSCs), predominantly squamous cell carcinomas (SCCs).
T3 312-534 Sentence denotes We have analyzed skin lesions from RTRs with aggressive tumors for p53 gene modifications, the presence of Human Papillomas Virus (HPV) DNA in relation to the p53 codon 72 genotype and polymorphisms of the XPD repair gene.
T4 535-702 Sentence denotes We detected 24 p53 mutations in 15/25 (60%) NMSCs, 1 deletion and 23 base substitutions, the majority (78%) being UV-specific C to T transitions at bipyrimidine sites.
T5 703-892 Sentence denotes Importantly, 35% (6/17) are tandem mutations, including 4 UV signature CC to TT transitions possibly linked to modulated DNA repair caused by the immunosuppressive drug cyclosporin A (CsA).
T6 893-1043 Sentence denotes We found 8 p53 mutations in 7/17 (41%) precancerous actinic keratosis (AK), suggesting that p53 mutations are early events in RTR skin carcinogenesis.
T7 1044-1137 Sentence denotes Immunohistochemical analysis shows a good correlation between p53 accumulation and mutations.
T8 1138-1230 Sentence denotes HPV DNA was detected in 78% of skin lesions (60% Basal Cell Carcinomas, 82%AK and 79% SCCs).
T9 1231-1401 Sentence denotes Thus, immunosuppression has increased the risk of infections by HPVs, predominantly epidermodysplasia verruciformis, speculated to play a role in skin cancer development.
T10 1402-1462 Sentence denotes No association is found between HPV status and p53 mutation.
T11 1463-1572 Sentence denotes Moreover, p53 codon 72 or frequencies of three XPD genotypes of RTRs are comparable with control populations.
T12 1573-1827 Sentence denotes The p53 mutation spectrum, presenting a high level of CC to TT mutations, shows that the UV component of sunlight is the major risk factor and modulated DNA repair by immunosuppressive drug treatment may be significant in the skin carcinogenesis of RTRs.

LitCoin-entities-OrganismTaxon-PD

Id Subject Object Predicate Lexical cue db_id
T1 419-441 OrganismTaxon denotes Human Papillomas Virus NCBItxid:10566
T2 443-446 OrganismTaxon denotes HPV NCBItxid:10566
T3 475-480 OrganismTaxon denotes codon NCBItxid:79338
T4 1138-1141 OrganismTaxon denotes HPV NCBItxid:10566
T5 1434-1437 OrganismTaxon denotes HPV NCBItxid:10566
T6 1477-1482 OrganismTaxon denotes codon NCBItxid:79338

LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
3564 12-23 DiseaseOrPhenotypicFeature denotes skin cancer MESH:D012878
3565 74-82 OrganismTaxon denotes patients NCBITaxon:9606
3566 123-131 SequenceVariant denotes CC to TT c|SUB|C||T
3567 149-152 GeneOrGeneProduct denotes p53 NCBIGene:7157
3568 230-255 DiseaseOrPhenotypicFeature denotes non-melanoma skin cancers MESH:D012878
3569 257-262 DiseaseOrPhenotypicFeature denotes NMSCs MESH:D012878
3570 279-303 DiseaseOrPhenotypicFeature denotes squamous cell carcinomas MESH:D002294
3571 305-309 DiseaseOrPhenotypicFeature denotes SCCs MESH:D002294
3572 329-341 DiseaseOrPhenotypicFeature denotes skin lesions MESH:D012871
3573 368-374 DiseaseOrPhenotypicFeature denotes tumors MESH:D009369
3574 379-382 GeneOrGeneProduct denotes p53 NCBIGene:7157
3575 419-441 OrganismTaxon denotes Human Papillomas Virus NCBITaxon:10566
3576 443-446 OrganismTaxon denotes HPV NCBITaxon:10566
3577 471-474 GeneOrGeneProduct denotes p53 NCBIGene:7157
3578 518-521 GeneOrGeneProduct denotes XPD NCBIGene:2068
3579 550-553 GeneOrGeneProduct denotes p53 NCBIGene:7157
3580 579-584 DiseaseOrPhenotypicFeature denotes NMSCs MESH:D012878
3581 661-667 SequenceVariant denotes C to T c|SUB|C||T
3582 774-782 SequenceVariant denotes CC to TT c|SUB|C||T
3583 872-885 ChemicalEntity denotes cyclosporin A MESH:D016572
3584 887-890 ChemicalEntity denotes CsA MESH:D016572
3585 904-907 GeneOrGeneProduct denotes p53 NCBIGene:7157
3586 932-944 DiseaseOrPhenotypicFeature denotes precancerous MESH:D011230
3587 945-962 DiseaseOrPhenotypicFeature denotes actinic keratosis MESH:D055623
3588 964-966 DiseaseOrPhenotypicFeature denotes AK MESH:D055623
3589 985-988 GeneOrGeneProduct denotes p53 NCBIGene:7157
3590 1023-1042 DiseaseOrPhenotypicFeature denotes skin carcinogenesis MESH:D012878
3591 1106-1109 GeneOrGeneProduct denotes p53 NCBIGene:7157
3592 1138-1141 OrganismTaxon denotes HPV NCBITaxon:10566
3593 1169-1181 DiseaseOrPhenotypicFeature denotes skin lesions MESH:D012871
3594 1187-1208 DiseaseOrPhenotypicFeature denotes Basal Cell Carcinomas MESH:D002280
3595 1213-1215 DiseaseOrPhenotypicFeature denotes AK MESH:D055623
3596 1224-1228 DiseaseOrPhenotypicFeature denotes SCCs MESH:D002294
3597 1281-1291 DiseaseOrPhenotypicFeature denotes infections MESH:D007239
3598 1295-1299 OrganismTaxon denotes HPVs NCBITaxon:10566
3599 1315-1346 DiseaseOrPhenotypicFeature denotes epidermodysplasia verruciformis MESH:D004819
3600 1377-1388 DiseaseOrPhenotypicFeature denotes skin cancer MESH:D012878
3601 1434-1437 OrganismTaxon denotes HPV NCBITaxon:10566
3602 1449-1452 GeneOrGeneProduct denotes p53 NCBIGene:7157
3603 1473-1476 GeneOrGeneProduct denotes p53 NCBIGene:7157
3604 1510-1513 GeneOrGeneProduct denotes XPD NCBIGene:2068
3605 1577-1580 GeneOrGeneProduct denotes p53 NCBIGene:7157
3606 1627-1635 SequenceVariant denotes CC to TT c|SUB|C||T
3607 1799-1818 DiseaseOrPhenotypicFeature denotes skin carcinogenesis MESH:D012878

LitCoin_Mondo

Id Subject Object Predicate Lexical cue mondo_id
T1 12-23 DiseaseOrPhenotypicFeature denotes skin cancer 0002898
T2 17-23 DiseaseOrPhenotypicFeature denotes cancer 0004992
T3 234-242 DiseaseOrPhenotypicFeature denotes melanoma 0005105
T4 243-255 DiseaseOrPhenotypicFeature denotes skin cancers 0002898
T5 279-303 DiseaseOrPhenotypicFeature denotes squamous cell carcinomas 0005096
T6 425-435 DiseaseOrPhenotypicFeature denotes Papillomas 0002363
T7 945-962 DiseaseOrPhenotypicFeature denotes actinic keratosis 0005173
T8 953-962 DiseaseOrPhenotypicFeature denotes keratosis 0006566
T9 1187-1208 DiseaseOrPhenotypicFeature denotes Basal Cell Carcinomas 0020804
T10 1315-1346 DiseaseOrPhenotypicFeature denotes epidermodysplasia verruciformis 0009176
T11 1377-1388 DiseaseOrPhenotypicFeature denotes skin cancer 0002898
T12 1382-1388 DiseaseOrPhenotypicFeature denotes cancer 0004992

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T1 89-93 GeneOrGeneProduct denotes high
T2 288-292 GeneOrGeneProduct denotes cell
T3 334-341 GeneOrGeneProduct denotes lesions
T4 824-834 GeneOrGeneProduct denotes DNA repair
T5 1003-1008 GeneOrGeneProduct denotes early
T6 1174-1181 GeneOrGeneProduct denotes lesions
T7 1613-1617 GeneOrGeneProduct denotes high
T8 1694-1699 GeneOrGeneProduct denotes major
T9 1705-1711 GeneOrGeneProduct denotes factor
T10 1726-1736 GeneOrGeneProduct denotes DNA repair

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T1 12-16 GeneOrGeneProduct denotes skin
T2 29-36 GeneOrGeneProduct denotes factors
T3 89-93 GeneOrGeneProduct denotes high
T4 123-131 GeneOrGeneProduct denotes CC to TT
T5 132-141 GeneOrGeneProduct denotes mutations
T6 243-247 GeneOrGeneProduct denotes skin
T7 288-292 GeneOrGeneProduct denotes cell
T8 329-333 GeneOrGeneProduct denotes skin
T9 334-341 GeneOrGeneProduct denotes lesions
T10 368-374 GeneOrGeneProduct denotes tumors
T11 554-563 GeneOrGeneProduct denotes mutations
T12 564-569 GeneOrGeneProduct denotes in 15
T13 604-608 GeneOrGeneProduct denotes base
T14 628-636 GeneOrGeneProduct denotes majority
T15 738-747 GeneOrGeneProduct denotes mutations
T16 774-782 GeneOrGeneProduct denotes CC to TT
T17 804-810 GeneOrGeneProduct denotes linked
T18 824-834 GeneOrGeneProduct denotes DNA repair
T19 884-891 GeneOrGeneProduct denotes A (CsA)
T20 908-917 GeneOrGeneProduct denotes mutations
T21 945-952 GeneOrGeneProduct denotes actinic
T22 989-998 GeneOrGeneProduct denotes mutations
T23 1003-1008 GeneOrGeneProduct denotes early
T24 1023-1027 GeneOrGeneProduct denotes skin
T25 1127-1136 GeneOrGeneProduct denotes mutations
T26 1169-1173 GeneOrGeneProduct denotes skin
T27 1174-1181 GeneOrGeneProduct denotes lesions
T28 1193-1197 GeneOrGeneProduct denotes Cell
T29 1377-1381 GeneOrGeneProduct denotes skin
T30 1453-1461 GeneOrGeneProduct denotes mutation
T31 1483-1488 GeneOrGeneProduct denotes 72 or
T32 1489-1500 GeneOrGeneProduct denotes frequencies
T33 1581-1589 GeneOrGeneProduct denotes mutation
T34 1613-1617 GeneOrGeneProduct denotes high
T35 1627-1635 GeneOrGeneProduct denotes CC to TT
T36 1636-1645 GeneOrGeneProduct denotes mutations
T37 1694-1699 GeneOrGeneProduct denotes major
T38 1705-1711 GeneOrGeneProduct denotes factor
T39 1726-1736 GeneOrGeneProduct denotes DNA repair
T40 1799-1803 GeneOrGeneProduct denotes skin

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T1 12-23 DiseaseOrPhenotypicFeature denotes skin cancer D012878
T2 234-242 DiseaseOrPhenotypicFeature denotes melanoma D008545
T3 243-255 DiseaseOrPhenotypicFeature denotes skin cancers D012878
T4 279-303 DiseaseOrPhenotypicFeature denotes squamous cell carcinomas D002294
T5 305-309 DiseaseOrPhenotypicFeature denotes SCCs D002294
T6 368-374 DiseaseOrPhenotypicFeature denotes tumors D009369
T7 425-435 DiseaseOrPhenotypicFeature denotes Papillomas D010212
T8 932-944 DiseaseOrPhenotypicFeature denotes precancerous DISEASE
T9 945-962 DiseaseOrPhenotypicFeature denotes actinic keratosis D055623
T10 964-966 DiseaseOrPhenotypicFeature denotes AK D055623
T11 1028-1042 DiseaseOrPhenotypicFeature denotes carcinogenesis D063646
T12 1187-1208 DiseaseOrPhenotypicFeature denotes Basal Cell Carcinomas D002280
T13 1213-1215 DiseaseOrPhenotypicFeature denotes AK D055623
T14 1224-1228 DiseaseOrPhenotypicFeature denotes SCCs D002294
T15 1281-1291 DiseaseOrPhenotypicFeature denotes infections D007239
T16 1315-1346 DiseaseOrPhenotypicFeature denotes epidermodysplasia verruciformis D004819
T17 1377-1388 DiseaseOrPhenotypicFeature denotes skin cancer D012878
T18 1804-1818 DiseaseOrPhenotypicFeature denotes carcinogenesis D063646

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T1 12-23 DiseaseOrPhenotypicFeature denotes skin cancer 0002898
T2 123-125 DiseaseOrPhenotypicFeature denotes CC 0019087
T3 230-255 DiseaseOrPhenotypicFeature denotes non-melanoma skin cancers 0002656
T4 279-303 DiseaseOrPhenotypicFeature denotes squamous cell carcinomas 0005096
T5 305-309 DiseaseOrPhenotypicFeature denotes SCCs 0005096
T6 329-333 DiseaseOrPhenotypicFeature denotes skin 0002531
T7 518-521 DiseaseOrPhenotypicFeature denotes XPD 0010212
T8 774-776 DiseaseOrPhenotypicFeature denotes CC 0019087
T9 945-962 DiseaseOrPhenotypicFeature denotes actinic keratosis 0005173
T10 964-966 DiseaseOrPhenotypicFeature denotes AK 0005173
T11 1023-1027 DiseaseOrPhenotypicFeature denotes skin 0002531
T12 1169-1173 DiseaseOrPhenotypicFeature denotes skin 0002531
T13 1213-1215 DiseaseOrPhenotypicFeature denotes AK 0005173
T14 1224-1228 DiseaseOrPhenotypicFeature denotes SCCs 0005096
T15 1315-1346 DiseaseOrPhenotypicFeature denotes epidermodysplasia verruciformis 0009176
T16 1377-1388 DiseaseOrPhenotypicFeature denotes skin cancer 0002898
T17 1510-1513 DiseaseOrPhenotypicFeature denotes XPD 0010212
T18 1627-1629 DiseaseOrPhenotypicFeature denotes CC 0019087
T19 1799-1803 DiseaseOrPhenotypicFeature denotes skin 0002531

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T1 12-23 DiseaseOrPhenotypicFeature denotes skin cancer D012878
T2 234-242 DiseaseOrPhenotypicFeature denotes melanoma D008545
T3 243-255 DiseaseOrPhenotypicFeature denotes skin cancers D012878
T4 257-262 DiseaseOrPhenotypicFeature denotes NMSCs DISEASE
T5 279-303 DiseaseOrPhenotypicFeature denotes squamous cell carcinomas D002294
T6 305-309 DiseaseOrPhenotypicFeature denotes SCCs D002294
T7 329-341 DiseaseOrPhenotypicFeature denotes skin lesions DISEASE
T8 368-374 DiseaseOrPhenotypicFeature denotes tumors DISEASE|D009369
T10 425-435 DiseaseOrPhenotypicFeature denotes Papillomas D010212
T11 579-584 DiseaseOrPhenotypicFeature denotes NMSCs DISEASE
T12 932-944 DiseaseOrPhenotypicFeature denotes precancerous DISEASE
T13 945-962 DiseaseOrPhenotypicFeature denotes actinic keratosis D055623
T14 964-966 DiseaseOrPhenotypicFeature denotes AK D055623
T15 1028-1042 DiseaseOrPhenotypicFeature denotes carcinogenesis D063646
T16 1169-1181 DiseaseOrPhenotypicFeature denotes skin lesions DISEASE
T17 1187-1208 DiseaseOrPhenotypicFeature denotes Basal Cell Carcinomas D002280
T18 1213-1215 DiseaseOrPhenotypicFeature denotes AK D055623
T19 1224-1228 DiseaseOrPhenotypicFeature denotes SCCs D002294
T20 1281-1291 DiseaseOrPhenotypicFeature denotes infections D007239
T21 1315-1346 DiseaseOrPhenotypicFeature denotes epidermodysplasia verruciformis D004819
T22 1377-1388 DiseaseOrPhenotypicFeature denotes skin cancer D012878
T23 1804-1818 DiseaseOrPhenotypicFeature denotes carcinogenesis D063646

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T1 12-23 DiseaseOrPhenotypicFeature denotes skin cancer D012878
T2 234-242 DiseaseOrPhenotypicFeature denotes melanoma D008545
T3 243-255 DiseaseOrPhenotypicFeature denotes skin cancers D012878
T4 257-262 DiseaseOrPhenotypicFeature denotes NMSCs DISEASE
T5 279-303 DiseaseOrPhenotypicFeature denotes squamous cell carcinomas D002294
T6 305-309 DiseaseOrPhenotypicFeature denotes SCCs D002294
T7 329-341 DiseaseOrPhenotypicFeature denotes skin lesions DISEASE
T8 368-374 DiseaseOrPhenotypicFeature denotes tumors D009369
T9 425-435 DiseaseOrPhenotypicFeature denotes Papillomas D010212
T10 579-584 DiseaseOrPhenotypicFeature denotes NMSCs DISEASE
T11 932-944 DiseaseOrPhenotypicFeature denotes precancerous DISEASE
T12 945-962 DiseaseOrPhenotypicFeature denotes actinic keratosis D055623
T13 964-966 DiseaseOrPhenotypicFeature denotes AK D055623
T14 1028-1042 DiseaseOrPhenotypicFeature denotes carcinogenesis D063646
T15 1169-1181 DiseaseOrPhenotypicFeature denotes skin lesions DISEASE
T16 1187-1208 DiseaseOrPhenotypicFeature denotes Basal Cell Carcinomas D002280
T17 1213-1215 DiseaseOrPhenotypicFeature denotes AK D055623
T18 1224-1228 DiseaseOrPhenotypicFeature denotes SCCs D002294
T19 1315-1346 DiseaseOrPhenotypicFeature denotes epidermodysplasia verruciformis D004819
T20 1377-1388 DiseaseOrPhenotypicFeature denotes skin cancer D012878
T21 1804-1818 DiseaseOrPhenotypicFeature denotes carcinogenesis D063646

LitCoin-NCBITaxon-2

Id Subject Object Predicate Lexical cue
T1 74-82 OrganismTaxon denotes patients
T2 419-441 OrganismTaxon denotes Human Papillomas Virus

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label
T21 1804-1818 DiseaseOrPhenotypicFeature denotes carcinogenesis D063646
T20 1377-1388 DiseaseOrPhenotypicFeature denotes skin cancer D012878
T19 1315-1346 DiseaseOrPhenotypicFeature denotes epidermodysplasia verruciformis D004819
T18 1224-1228 DiseaseOrPhenotypicFeature denotes SCCs D002294
T17 1213-1215 DiseaseOrPhenotypicFeature denotes AK D055623
T16 1187-1208 DiseaseOrPhenotypicFeature denotes Basal Cell Carcinomas D002280
T15 1169-1181 DiseaseOrPhenotypicFeature denotes skin lesions DISEASE
T14 1028-1042 DiseaseOrPhenotypicFeature denotes carcinogenesis D063646
T13 964-966 DiseaseOrPhenotypicFeature denotes AK D055623
T12 945-962 DiseaseOrPhenotypicFeature denotes actinic keratosis D055623
T11 932-944 DiseaseOrPhenotypicFeature denotes precancerous DISEASE
T10 579-584 DiseaseOrPhenotypicFeature denotes NMSCs DISEASE
T9 425-435 DiseaseOrPhenotypicFeature denotes Papillomas D010212
T8 368-374 DiseaseOrPhenotypicFeature denotes tumors D009369
T7 329-341 DiseaseOrPhenotypicFeature denotes skin lesions DISEASE
T6 305-309 DiseaseOrPhenotypicFeature denotes SCCs D002294
T5 279-303 DiseaseOrPhenotypicFeature denotes squamous cell carcinomas D002294
T4 257-262 DiseaseOrPhenotypicFeature denotes NMSCs DISEASE
T3 243-255 DiseaseOrPhenotypicFeature denotes skin cancers D012878
T2 234-242 DiseaseOrPhenotypicFeature denotes melanoma D008545
T1 12-23 DiseaseOrPhenotypicFeature denotes skin cancer D012878
T86636 419-441 OrganismTaxon denotes Human Papillomas Virus
T1457 74-82 OrganismTaxon denotes patients

DisGeNET

Id Subject Object Predicate Lexical cue
T0 904-907 gene:7157 denotes p53
T1 945-962 disease:C0022602 denotes actinic keratosis
T2 904-907 gene:7157 denotes p53
T3 964-966 disease:C0022602 denotes AK
T4 904-907 gene:7157 denotes p53
T5 1023-1042 disease:C1519346 denotes skin carcinogenesis
T6 985-988 gene:7157 denotes p53
T7 945-962 disease:C0022602 denotes actinic keratosis
T8 985-988 gene:7157 denotes p53
T9 1023-1042 disease:C1519346 denotes skin carcinogenesis
T10 1019-1022 gene:2649 denotes RTR
T11 945-962 disease:C0022602 denotes actinic keratosis
T12 1019-1022 gene:2649 denotes RTR
T13 1023-1042 disease:C1519346 denotes skin carcinogenesis
R1 T0 T1 associated_with p53,actinic keratosis
R2 T2 T3 associated_with p53,AK
R3 T4 T5 associated_with p53,skin carcinogenesis
R4 T6 T7 associated_with p53,actinic keratosis
R5 T8 T9 associated_with p53,skin carcinogenesis
R6 T10 T11 associated_with RTR,actinic keratosis
R7 T12 T13 associated_with RTR,skin carcinogenesis

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 234-242 HP_0002861 denotes melanoma
T2 234-247 HP_0012056 denotes melanoma skin
T3 243-255 HP_0008069 denotes skin cancers
T4 248-255 HP_0002664 denotes cancers
T5 279-303 HP_0002860 denotes squamous cell carcinomas
T6 357-367 HP_0000718 denotes aggressive
T7 368-374 HP_0002664 denotes tumors
T8 425-435 HP_0012740 denotes Papillomas
T9 1187-1208 HP_0002671 denotes Basal Cell Carcinomas
T10 1377-1388 HP_0008069 denotes skin cancer
T11 1382-1388 HP_0002664 denotes cancer
T1 234-242 HP_0002861 denotes melanoma
T2 234-247 HP_0012056 denotes melanoma skin
T3 243-255 HP_0008069 denotes skin cancers
T4 248-255 HP_0002664 denotes cancers
T5 279-303 HP_0002860 denotes squamous cell carcinomas
T6 357-367 HP_0000718 denotes aggressive
T7 368-374 HP_0002664 denotes tumors
T8 425-435 HP_0012740 denotes Papillomas
T9 1187-1208 HP_0002671 denotes Basal Cell Carcinomas
T10 1377-1388 HP_0008069 denotes skin cancer
T11 1382-1388 HP_0002664 denotes cancer

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
17065198-0#149#152#gene7157 149-152 gene7157 denotes p53
17065198-0#9#23#diseaseC0007114 9-23 diseaseC0007114 denotes of skin cancer
17065198-11#4#7#gene7157 1577-1580 gene7157 denotes p53
17065198-11#226#245#diseaseC1519346 1799-1818 diseaseC1519346 denotes skin carcinogenesis
17065198-5#11#14#gene7157 904-907 gene7157 denotes p53
17065198-5#92#95#gene7157 985-988 gene7157 denotes p53
17065198-5#52#69#diseaseC0022602 945-962 diseaseC0022602 denotes actinic keratosis
17065198-5#71#73#diseaseC0022602 964-966 diseaseC0022602 denotes AK
17065198-5#52#69#diseaseC0022602 945-962 diseaseC0022602 denotes actinic keratosis
149#152#gene71579#23#diseaseC0007114 17065198-0#149#152#gene7157 17065198-0#9#23#diseaseC0007114 associated_with p53,of skin cancer
4#7#gene7157226#245#diseaseC1519346 17065198-11#4#7#gene7157 17065198-11#226#245#diseaseC1519346 associated_with p53,skin carcinogenesis
11#14#gene715752#69#diseaseC0022602 17065198-5#11#14#gene7157 17065198-5#52#69#diseaseC0022602 associated_with p53,actinic keratosis
11#14#gene715771#73#diseaseC0022602 17065198-5#11#14#gene7157 17065198-5#71#73#diseaseC0022602 associated_with p53,AK
11#14#gene715752#69#diseaseC0022602 17065198-5#11#14#gene7157 17065198-5#52#69#diseaseC0022602 associated_with p53,actinic keratosis
92#95#gene715752#69#diseaseC0022602 17065198-5#92#95#gene7157 17065198-5#52#69#diseaseC0022602 associated_with p53,actinic keratosis
92#95#gene715771#73#diseaseC0022602 17065198-5#92#95#gene7157 17065198-5#71#73#diseaseC0022602 associated_with p53,AK
92#95#gene715752#69#diseaseC0022602 17065198-5#92#95#gene7157 17065198-5#52#69#diseaseC0022602 associated_with p53,actinic keratosis