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LitCoin-sentences

Id Subject Object Predicate Lexical cue
T1 0-100 Sentence denotes DNA damage and repair in gastric cancer--a correlation with the hOGG1 and RAD51 genes polymorphisms.
T2 101-239 Sentence denotes The cell's susceptibility to mutagens and its ability to repair DNA lesions are important for cancer induction, promotion and progression.
T3 240-376 Sentence denotes Both the mutagens' sensitivity and the efficacy of DNA repair may be affected by variation in several genes, including DNA repair genes.
T4 377-505 Sentence denotes The hOGG1 gene encodes glycosylase of base excision repair and RAD51 specifies a key protein in homologues recombination repair.
T5 506-606 Sentence denotes Both can be involved in the repair of oxidative DNA lesions, which can contribute to stomach cancer.
T6 607-845 Sentence denotes In the present work we determined the level of basal and oxidative DNA damage and the kinetics of removal of DNA damage induced by hydrogen peroxide in peripheral blood lymphocytes of 30 gastric cancer patients and 30 healthy individuals.
T7 846-1226 Sentence denotes The metrics from DNA damage and repair study were correlated with the genotypes of common polymorphisms of the hOGG1 and RAD51 genes: a G-->C transversion at 1245 position of the hOGG1 gene producing a Ser-->Cys substitution at the codon 326 (the Ser326Cys polymorphism) and a G-->C substitution at position 135 (5'-untranslated region) of the RAD51 gene (the G135C polymorphism).
T8 1227-1470 Sentence denotes DNA damage and repair were evaluated by alkaline single cell gel electrophoresis (comet assay) assisted by DNA repair enzymes: endonuclease III (Nth) and formamidopyrimidine-DNA glycosylase (Fpg), preferentially recognizing oxidized DNA bases.
T9 1471-1569 Sentence denotes The genotypes of the polymorphism were determined by restriction fragment length polymorphism PCR.
T10 1570-1744 Sentence denotes We observed a strong association between gastric cancer occurrence, impaired DNA repair in human lymphocytes and the G/C genotype of the G135C polymorphism of the RAD51 gene.
T11 1745-1893 Sentence denotes Moreover, there was a strong correlation between that genotype and stomach cancer occurrence in subjects with high level of oxidatively damaged DNA.
T12 1894-2102 Sentence denotes We did not observe any correlation between the Ser1245Cys polymorphism of the hOGG1 gene and gastric cancer, including subjects with impaired DNA repair and/or high levels of endogenous oxidative DNA lesions.
T13 2103-2423 Sentence denotes Therefore, our result suggest that the G135C polymorphism of the RAD51 gene may be linked with gastric cancer by the modulation of the cellular response to oxidative stress and this polymorphism may be a useful additional marker in this disease along with the genetic or/and environmental indicators of oxidative stress.

LitCoin-entities-OrganismTaxon-PD

Id Subject Object Predicate Lexical cue db_id
T1 1078-1083 OrganismTaxon denotes codon NCBItxid:79338
T2 1309-1314 OrganismTaxon denotes comet NCBItxid:302767
T3 1661-1666 OrganismTaxon denotes human NCBItxid:9606
T4 2392-2402 OrganismTaxon denotes indicators NCBItxid:189528

LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
3207 25-39 DiseaseOrPhenotypicFeature denotes gastric cancer MESH:D013274
3208 64-69 GeneOrGeneProduct denotes hOGG1 NCBIGene:4968
3209 74-79 GeneOrGeneProduct denotes RAD51 NCBIGene:5888
3210 195-201 DiseaseOrPhenotypicFeature denotes cancer MESH:D009369
3211 381-386 GeneOrGeneProduct denotes hOGG1 NCBIGene:4968
3212 440-445 GeneOrGeneProduct denotes RAD51 NCBIGene:5888
3213 591-605 DiseaseOrPhenotypicFeature denotes stomach cancer MESH:D013274
3214 738-755 ChemicalEntity denotes hydrogen peroxide MESH:D006861
3215 794-808 DiseaseOrPhenotypicFeature denotes gastric cancer MESH:D013274
3216 809-817 OrganismTaxon denotes patients NCBITaxon:9606
3217 957-962 GeneOrGeneProduct denotes hOGG1 NCBIGene:4968
3218 967-972 GeneOrGeneProduct denotes RAD51 NCBIGene:5888
3219 982-1017 SequenceVariant denotes G-->C transversion at 1245 position DBSNP:rs1052133
3220 1025-1030 GeneOrGeneProduct denotes hOGG1 NCBIGene:4968
3221 1048-1087 SequenceVariant denotes Ser-->Cys substitution at the codon 326 DBSNP:rs1052133
3222 1093-1102 SequenceVariant denotes Ser326Cys DBSNP:rs1052133
3223 1123-1157 SequenceVariant denotes G-->C substitution at position 135 g|SUB|G|135|C
3224 1190-1195 GeneOrGeneProduct denotes RAD51 NCBIGene:5888
3225 1206-1211 SequenceVariant denotes G135C g|SUB|G|135|C
3226 1354-1370 GeneOrGeneProduct denotes endonuclease III NCBIGene:4913
3227 1372-1375 GeneOrGeneProduct denotes Nth NCBIGene:4913
3228 1381-1416 GeneOrGeneProduct denotes formamidopyrimidine-DNA glycosylase NCBIGene:79661
3229 1418-1421 GeneOrGeneProduct denotes Fpg NCBIGene:79661
3230 1611-1625 DiseaseOrPhenotypicFeature denotes gastric cancer MESH:D013274
3231 1661-1666 OrganismTaxon denotes human NCBITaxon:9606
3232 1687-1690 SequenceVariant denotes G/C g|SUB|G||C
3233 1707-1712 SequenceVariant denotes G135C g|SUB|G|135|C
3234 1733-1738 GeneOrGeneProduct denotes RAD51 NCBIGene:5888
3235 1812-1826 DiseaseOrPhenotypicFeature denotes stomach cancer MESH:D013274
3236 1941-1951 SequenceVariant denotes Ser1245Cys DBSNP:rs1052133
3237 1972-1977 GeneOrGeneProduct denotes hOGG1 NCBIGene:4968
3238 1987-2001 DiseaseOrPhenotypicFeature denotes gastric cancer MESH:D013274
3239 2142-2147 SequenceVariant denotes G135C g|SUB|G|135|C
3240 2168-2173 GeneOrGeneProduct denotes RAD51 NCBIGene:5888
3241 2198-2212 DiseaseOrPhenotypicFeature denotes gastric cancer MESH:D013274

LitCoin_Mondo

Id Subject Object Predicate Lexical cue mondo_id
T1 25-39 DiseaseOrPhenotypicFeature denotes gastric cancer 0001056
T2 33-39 DiseaseOrPhenotypicFeature denotes cancer 0004992
T3 195-201 DiseaseOrPhenotypicFeature denotes cancer 0004992
T4 249-270 DiseaseOrPhenotypicFeature denotes mutagens' sensitivity 0012501
T5 599-605 DiseaseOrPhenotypicFeature denotes cancer 0004992
T6 794-808 DiseaseOrPhenotypicFeature denotes gastric cancer 0001056
T7 802-808 DiseaseOrPhenotypicFeature denotes cancer 0004992
T8 1611-1625 DiseaseOrPhenotypicFeature denotes gastric cancer 0001056
T9 1619-1625 DiseaseOrPhenotypicFeature denotes cancer 0004992
T10 1820-1826 DiseaseOrPhenotypicFeature denotes cancer 0004992
T11 1987-2001 DiseaseOrPhenotypicFeature denotes gastric cancer 0001056
T12 1995-2001 DiseaseOrPhenotypicFeature denotes cancer 0004992
T13 2198-2212 DiseaseOrPhenotypicFeature denotes gastric cancer 0001056
T14 2206-2212 DiseaseOrPhenotypicFeature denotes cancer 0004992

LitCoin-SeqVar

Id Subject Object Predicate Lexical cue
T1 982-987 SequenceVariant denotes G-->C
T2 1093-1102 SequenceVariant denotes Ser326Cys
T3 1123-1128 SequenceVariant denotes G-->C
T4 1206-1211 SequenceVariant denotes G135C
T5 1707-1712 SequenceVariant denotes G135C
T6 1941-1951 SequenceVariant denotes Ser1245Cys
T7 2142-2147 SequenceVariant denotes G135C

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T1 0-21 GeneOrGeneProduct denotes DNA damage and repair
T2 64-69 GeneOrGeneProduct denotes hOGG1
T3 74-79 GeneOrGeneProduct denotes RAD51
T4 105-111 GeneOrGeneProduct denotes cell's
T5 169-176 GeneOrGeneProduct denotes lesions
T6 291-301 GeneOrGeneProduct denotes DNA repair
T7 359-369 GeneOrGeneProduct denotes DNA repair
T8 381-386 GeneOrGeneProduct denotes hOGG1
T9 400-411 GeneOrGeneProduct denotes glycosylase
T10 415-419 GeneOrGeneProduct denotes base
T11 420-428 GeneOrGeneProduct denotes excision
T12 440-445 GeneOrGeneProduct denotes RAD51
T13 462-469 GeneOrGeneProduct denotes protein
T14 473-483 GeneOrGeneProduct denotes homologues
T15 484-497 GeneOrGeneProduct denotes recombination
T16 558-565 GeneOrGeneProduct denotes lesions
T17 630-644 GeneOrGeneProduct denotes determined the
T18 678-684 GeneOrGeneProduct denotes damage
T19 720-726 GeneOrGeneProduct denotes damage
T20 727-734 GeneOrGeneProduct denotes induced
T21 747-755 GeneOrGeneProduct denotes peroxide
T22 776-787 GeneOrGeneProduct denotes lymphocytes
T23 863-884 GeneOrGeneProduct denotes DNA damage and repair
T24 957-962 GeneOrGeneProduct denotes hOGG1
T25 967-972 GeneOrGeneProduct denotes RAD51
T26 973-981 GeneOrGeneProduct denotes genes: a
T27 982-987 GeneOrGeneProduct denotes G-->C
T28 1025-1030 GeneOrGeneProduct denotes hOGG1
T29 1046-1051 GeneOrGeneProduct denotes a Ser
T30 1054-1057 GeneOrGeneProduct denotes Cys
T31 1123-1128 GeneOrGeneProduct denotes G-->C
T32 1190-1195 GeneOrGeneProduct denotes RAD51
T33 1206-1211 GeneOrGeneProduct denotes G135C
T34 1227-1248 GeneOrGeneProduct denotes DNA damage and repair
T35 1283-1287 GeneOrGeneProduct denotes cell
T36 1288-1291 GeneOrGeneProduct denotes gel
T37 1309-1314 GeneOrGeneProduct denotes comet
T38 1334-1344 GeneOrGeneProduct denotes DNA repair
T39 1345-1352 GeneOrGeneProduct denotes enzymes
T40 1354-1370 GeneOrGeneProduct denotes endonuclease III
T41 1381-1416 GeneOrGeneProduct denotes formamidopyrimidine-DNA glycosylase
T42 1418-1421 GeneOrGeneProduct denotes Fpg
T43 1464-1469 GeneOrGeneProduct denotes bases
T44 1510-1520 GeneOrGeneProduct denotes determined
T45 1647-1657 GeneOrGeneProduct denotes DNA repair
T46 1667-1678 GeneOrGeneProduct denotes lymphocytes
T47 1687-1690 GeneOrGeneProduct denotes G/C
T48 1707-1712 GeneOrGeneProduct denotes G135C
T49 1733-1738 GeneOrGeneProduct denotes RAD51
T50 1855-1859 GeneOrGeneProduct denotes high
T51 1881-1888 GeneOrGeneProduct denotes damaged
T52 1972-1977 GeneOrGeneProduct denotes hOGG1
T53 2036-2046 GeneOrGeneProduct denotes DNA repair
T54 2054-2058 GeneOrGeneProduct denotes high
T55 2094-2101 GeneOrGeneProduct denotes lesions
T56 2142-2147 GeneOrGeneProduct denotes G135C
T57 2168-2173 GeneOrGeneProduct denotes RAD51
T58 2186-2192 GeneOrGeneProduct denotes linked
T59 2298-2306 GeneOrGeneProduct denotes may be a

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T1 0-21 GeneOrGeneProduct denotes DNA damage and repair
T2 64-69 GeneOrGeneProduct denotes hOGG1
T3 74-79 GeneOrGeneProduct denotes RAD51
T4 169-176 GeneOrGeneProduct denotes lesions
T5 291-301 GeneOrGeneProduct denotes DNA repair
T6 359-369 GeneOrGeneProduct denotes DNA repair
T7 381-386 GeneOrGeneProduct denotes hOGG1
T8 400-411 GeneOrGeneProduct denotes glycosylase
T9 440-445 GeneOrGeneProduct denotes RAD51
T10 462-469 GeneOrGeneProduct denotes protein
T11 473-483 GeneOrGeneProduct denotes homologues
T12 484-497 GeneOrGeneProduct denotes recombination
T13 558-565 GeneOrGeneProduct denotes lesions
T14 747-755 GeneOrGeneProduct denotes peroxide
T15 776-787 GeneOrGeneProduct denotes lymphocytes
T16 863-884 GeneOrGeneProduct denotes DNA damage and repair
T17 957-962 GeneOrGeneProduct denotes hOGG1
T18 967-972 GeneOrGeneProduct denotes RAD51
T19 1025-1030 GeneOrGeneProduct denotes hOGG1
T20 1190-1195 GeneOrGeneProduct denotes RAD51
T21 1227-1248 GeneOrGeneProduct denotes DNA damage and repair
T22 1283-1287 GeneOrGeneProduct denotes cell
T23 1309-1314 GeneOrGeneProduct denotes comet
T24 1334-1344 GeneOrGeneProduct denotes DNA repair
T25 1354-1370 GeneOrGeneProduct denotes endonuclease III
T26 1381-1416 GeneOrGeneProduct denotes formamidopyrimidine-DNA glycosylase
T27 1418-1421 GeneOrGeneProduct denotes Fpg
T28 1647-1657 GeneOrGeneProduct denotes DNA repair
T29 1667-1678 GeneOrGeneProduct denotes lymphocytes
T30 1733-1738 GeneOrGeneProduct denotes RAD51
T31 1855-1859 GeneOrGeneProduct denotes high
T32 1972-1977 GeneOrGeneProduct denotes hOGG1
T33 2036-2046 GeneOrGeneProduct denotes DNA repair
T34 2054-2058 GeneOrGeneProduct denotes high
T35 2094-2101 GeneOrGeneProduct denotes lesions
T36 2168-2173 GeneOrGeneProduct denotes RAD51

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T1 25-39 DiseaseOrPhenotypicFeature denotes gastric cancer D013274
T2 195-201 DiseaseOrPhenotypicFeature denotes cancer D009369
T3 591-605 DiseaseOrPhenotypicFeature denotes stomach cancer D013274
T4 794-808 DiseaseOrPhenotypicFeature denotes gastric cancer D013274
T5 1611-1625 DiseaseOrPhenotypicFeature denotes gastric cancer D013274
T6 1812-1826 DiseaseOrPhenotypicFeature denotes stomach cancer D013274
T7 1987-2001 DiseaseOrPhenotypicFeature denotes gastric cancer D013274
T8 2198-2212 DiseaseOrPhenotypicFeature denotes gastric cancer D013274
T9 2340-2347 DiseaseOrPhenotypicFeature denotes disease D004194

LitCoin-GeneOrGeneProduct-v3

Id Subject Object Predicate Lexical cue
T1 64-69 GeneOrGeneProduct denotes hOGG1
T2 74-79 GeneOrGeneProduct denotes RAD51
T3 381-386 GeneOrGeneProduct denotes hOGG1
T4 400-411 GeneOrGeneProduct denotes glycosylase
T5 440-445 GeneOrGeneProduct denotes RAD51
T6 747-755 GeneOrGeneProduct denotes peroxide
T7 957-962 GeneOrGeneProduct denotes hOGG1
T8 967-972 GeneOrGeneProduct denotes RAD51
T9 1025-1030 GeneOrGeneProduct denotes hOGG1
T10 1190-1195 GeneOrGeneProduct denotes RAD51
T11 1309-1314 GeneOrGeneProduct denotes comet
T12 1334-1352 GeneOrGeneProduct denotes DNA repair enzymes
T13 1354-1370 GeneOrGeneProduct denotes endonuclease III
T14 1381-1416 GeneOrGeneProduct denotes formamidopyrimidine-DNA glycosylase
T15 1418-1421 GeneOrGeneProduct denotes Fpg
T16 1733-1738 GeneOrGeneProduct denotes RAD51
T17 1972-1977 GeneOrGeneProduct denotes hOGG1
T18 2168-2173 GeneOrGeneProduct denotes RAD51

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T1 25-39 DiseaseOrPhenotypicFeature denotes gastric cancer 0004950|0001056
T3 249-270 DiseaseOrPhenotypicFeature denotes mutagens' sensitivity 0012501
T4 511-514 DiseaseOrPhenotypicFeature denotes can 0012833
T5 573-576 DiseaseOrPhenotypicFeature denotes can 0012833
T6 591-605 DiseaseOrPhenotypicFeature denotes stomach cancer 0004950|0001056
T8 794-808 DiseaseOrPhenotypicFeature denotes gastric cancer 0004950|0001056
T10 1611-1625 DiseaseOrPhenotypicFeature denotes gastric cancer 0004950|0001056
T12 1812-1826 DiseaseOrPhenotypicFeature denotes stomach cancer 0004950|0001056
T14 1987-2001 DiseaseOrPhenotypicFeature denotes gastric cancer 0004950|0001056
T16 2198-2212 DiseaseOrPhenotypicFeature denotes gastric cancer 0004950|0001056

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T1 25-39 DiseaseOrPhenotypicFeature denotes gastric cancer D013274
T2 195-201 DiseaseOrPhenotypicFeature denotes cancer D009369
T3 591-605 DiseaseOrPhenotypicFeature denotes stomach cancer D013274
T4 794-808 DiseaseOrPhenotypicFeature denotes gastric cancer D013274
T5 1611-1625 DiseaseOrPhenotypicFeature denotes gastric cancer D013274
T6 1812-1826 DiseaseOrPhenotypicFeature denotes stomach cancer D013274
T7 1987-2001 DiseaseOrPhenotypicFeature denotes gastric cancer D013274
T8 2198-2212 DiseaseOrPhenotypicFeature denotes gastric cancer D013274
T9 2340-2347 DiseaseOrPhenotypicFeature denotes disease D004194

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T1 25-39 DiseaseOrPhenotypicFeature denotes gastric cancer D013274
T2 195-201 DiseaseOrPhenotypicFeature denotes cancer D009369
T3 591-605 DiseaseOrPhenotypicFeature denotes stomach cancer D013274
T4 794-808 DiseaseOrPhenotypicFeature denotes gastric cancer D013274
T5 1611-1625 DiseaseOrPhenotypicFeature denotes gastric cancer D013274
T6 1812-1826 DiseaseOrPhenotypicFeature denotes stomach cancer D013274
T7 1987-2001 DiseaseOrPhenotypicFeature denotes gastric cancer D013274
T8 2198-2212 DiseaseOrPhenotypicFeature denotes gastric cancer D013274

LitCoin-Chemical-MeSH-CHEBI

Id Subject Object Predicate Lexical cue ID:
T1 738-755 ChemicalEntity denotes hydrogen peroxide D006861|http://purl.obolibrary.org/obo/CHEBI_16240
T3 1048-1057 ChemicalEntity denotes Ser-->Cys http://purl.obolibrary.org/obo/CHEBI_157887
T4 1334-1352 ChemicalEntity denotes DNA repair enzymes D045643
T5 1354-1366 ChemicalEntity denotes endonuclease D004720
T6 1381-1416 ChemicalEntity denotes formamidopyrimidine-DNA glycosylase D043382
T7 1418-1421 ChemicalEntity denotes Fpg D043382

LitCoin-NCBITaxon-2

Id Subject Object Predicate Lexical cue
T1 809-817 OrganismTaxon denotes patients
T2 1309-1314 OrganismTaxon denotes comet
T3 1661-1666 OrganismTaxon denotes human

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label ID:
T7 1418-1421 ChemicalEntity denotes Fpg D043382
T6 1381-1416 ChemicalEntity denotes formamidopyrimidine-DNA glycosylase D043382
T5 1354-1366 ChemicalEntity denotes endonuclease D004720
T4 1334-1352 ChemicalEntity denotes DNA repair enzymes D045643
T3 1048-1057 ChemicalEntity denotes Ser-->Cys http://purl.obolibrary.org/obo/CHEBI_157887
T1 738-755 ChemicalEntity denotes hydrogen peroxide http://purl.obolibrary.org/obo/CHEBI_16240|D006861
T18 2168-2173 GeneOrGeneProduct denotes RAD51
T17 1972-1977 GeneOrGeneProduct denotes hOGG1
T16 1733-1738 GeneOrGeneProduct denotes RAD51
T15 1418-1421 GeneOrGeneProduct denotes Fpg
T14 1381-1416 GeneOrGeneProduct denotes formamidopyrimidine-DNA glycosylase
T13 1354-1370 GeneOrGeneProduct denotes endonuclease III
T12 1334-1352 GeneOrGeneProduct denotes DNA repair enzymes
T11 1309-1314 GeneOrGeneProduct denotes comet
T10 1190-1195 GeneOrGeneProduct denotes RAD51
T9 1025-1030 GeneOrGeneProduct denotes hOGG1
T8 967-972 GeneOrGeneProduct denotes RAD51
T80946 957-962 GeneOrGeneProduct denotes hOGG1
T18083 747-755 GeneOrGeneProduct denotes peroxide
T58515 440-445 GeneOrGeneProduct denotes RAD51
T17781 400-411 GeneOrGeneProduct denotes glycosylase
T56578 381-386 GeneOrGeneProduct denotes hOGG1
T2 74-79 GeneOrGeneProduct denotes RAD51
T59954 64-69 GeneOrGeneProduct denotes hOGG1
T55386 2198-2212 DiseaseOrPhenotypicFeature denotes gastric cancer D013274
T80296 1987-2001 DiseaseOrPhenotypicFeature denotes gastric cancer D013274
T96800 1812-1826 DiseaseOrPhenotypicFeature denotes stomach cancer D013274
T60355 1611-1625 DiseaseOrPhenotypicFeature denotes gastric cancer D013274
T78680 794-808 DiseaseOrPhenotypicFeature denotes gastric cancer D013274
T50979 591-605 DiseaseOrPhenotypicFeature denotes stomach cancer D013274
T11910 195-201 DiseaseOrPhenotypicFeature denotes cancer D009369
T65233 25-39 DiseaseOrPhenotypicFeature denotes gastric cancer D013274
T31577 1661-1666 OrganismTaxon denotes human
T71805 1309-1314 OrganismTaxon denotes comet
T82811 809-817 OrganismTaxon denotes patients
T21108 2142-2147 SequenceVariant denotes G135C
T271 1941-1951 SequenceVariant denotes Ser1245Cys
T98917 1707-1712 SequenceVariant denotes G135C
T68247 1206-1211 SequenceVariant denotes G135C
T74121 1123-1128 SequenceVariant denotes G-->C
T23925 1093-1102 SequenceVariant denotes Ser326Cys
T15264 982-987 SequenceVariant denotes G-->C

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 195-201 HP_0002664 denotes cancer
T2 599-605 HP_0002664 denotes cancer
T3 794-808 HP_0012126 denotes gastric cancer
T4 802-808 HP_0002664 denotes cancer
T5 1611-1625 HP_0012126 denotes gastric cancer
T6 1619-1625 HP_0002664 denotes cancer
T7 1812-1826 HP_0006753 denotes stomach cancer
T8 1812-1826 HP_0012126 denotes stomach cancer
T9 1820-1826 HP_0002664 denotes cancer
T10 1987-2001 HP_0012126 denotes gastric cancer
T11 1995-2001 HP_0002664 denotes cancer
T12 2198-2212 HP_0012126 denotes gastric cancer
T13 2206-2212 HP_0002664 denotes cancer

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
16843501-0#64#69#gene4968 1684-1977 gene4968 denotes he G/C genotype of the G135C polymorphism of the RAD51 gene. Moreover, there was a strong correlation between that genotype and stomach cancer occurrence in subjects with high level of oxidatively damaged DNA. We did not observe any correlation between the Ser1245Cys polymorphism of the hOGG1
16843501-0#74#79#gene5888 2168-2173 gene5888 denotes RAD51
16843501-0#25#39#diseaseC0024623 871-1096 diseaseC0024623 denotes ge and repair study were correlated with the genotypes of common polymorphisms of the hOGG1 and RAD51 genes: a G-->C transversion at 1245 position of the hOGG1 gene producing a Ser-->Cys substitution at the codon 326 (the Ser
16843501-0#25#39#diseaseC0699791 871-1096 diseaseC0699791 denotes ge and repair study were correlated with the genotypes of common polymorphisms of the hOGG1 and RAD51 genes: a G-->C transversion at 1245 position of the hOGG1 gene producing a Ser-->Cys substitution at the codon 326 (the Ser
16843501-0#25#39#diseaseC0024623 871-1096 diseaseC0024623 denotes ge and repair study were correlated with the genotypes of common polymorphisms of the hOGG1 and RAD51 genes: a G-->C transversion at 1245 position of the hOGG1 gene producing a Ser-->Cys substitution at the codon 326 (the Ser
16843501-0#25#39#diseaseC0699791 871-1096 diseaseC0699791 denotes ge and repair study were correlated with the genotypes of common polymorphisms of the hOGG1 and RAD51 genes: a G-->C transversion at 1245 position of the hOGG1 gene producing a Ser-->Cys substitution at the codon 326 (the Ser
64#69#gene496825#39#diseaseC0024623 16843501-0#64#69#gene4968 16843501-0#25#39#diseaseC0024623 associated_with "he G/C genotype of the G135C polymorphism of the RAD51 gene. Moreover, there was a strong correlation between that genotype and stomach cancer occurrence in subjects with high level of oxidatively damaged DNA. We did not observe any correlation between the Ser1245Cys polymorphism of the hOGG1",ge and repair study were correlated with the genotypes of common polymorphisms of the hOGG1 and RAD51 genes: a G-->C transversion at 1245 position of the hOGG1 gene producing a Ser-->Cys substitution at the codon 326 (the Ser
64#69#gene496825#39#diseaseC0699791 16843501-0#64#69#gene4968 16843501-0#25#39#diseaseC0699791 associated_with "he G/C genotype of the G135C polymorphism of the RAD51 gene. Moreover, there was a strong correlation between that genotype and stomach cancer occurrence in subjects with high level of oxidatively damaged DNA. We did not observe any correlation between the Ser1245Cys polymorphism of the hOGG1",ge and repair study were correlated with the genotypes of common polymorphisms of the hOGG1 and RAD51 genes: a G-->C transversion at 1245 position of the hOGG1 gene producing a Ser-->Cys substitution at the codon 326 (the Ser
64#69#gene496825#39#diseaseC0024623 16843501-0#64#69#gene4968 16843501-0#25#39#diseaseC0024623 associated_with "he G/C genotype of the G135C polymorphism of the RAD51 gene. Moreover, there was a strong correlation between that genotype and stomach cancer occurrence in subjects with high level of oxidatively damaged DNA. We did not observe any correlation between the Ser1245Cys polymorphism of the hOGG1",ge and repair study were correlated with the genotypes of common polymorphisms of the hOGG1 and RAD51 genes: a G-->C transversion at 1245 position of the hOGG1 gene producing a Ser-->Cys substitution at the codon 326 (the Ser
64#69#gene496825#39#diseaseC0699791 16843501-0#64#69#gene4968 16843501-0#25#39#diseaseC0699791 associated_with "he G/C genotype of the G135C polymorphism of the RAD51 gene. Moreover, there was a strong correlation between that genotype and stomach cancer occurrence in subjects with high level of oxidatively damaged DNA. We did not observe any correlation between the Ser1245Cys polymorphism of the hOGG1",ge and repair study were correlated with the genotypes of common polymorphisms of the hOGG1 and RAD51 genes: a G-->C transversion at 1245 position of the hOGG1 gene producing a Ser-->Cys substitution at the codon 326 (the Ser
74#79#gene588825#39#diseaseC0024623 16843501-0#74#79#gene5888 16843501-0#25#39#diseaseC0024623 associated_with RAD51,ge and repair study were correlated with the genotypes of common polymorphisms of the hOGG1 and RAD51 genes: a G-->C transversion at 1245 position of the hOGG1 gene producing a Ser-->Cys substitution at the codon 326 (the Ser
74#79#gene588825#39#diseaseC0699791 16843501-0#74#79#gene5888 16843501-0#25#39#diseaseC0699791 associated_with RAD51,ge and repair study were correlated with the genotypes of common polymorphisms of the hOGG1 and RAD51 genes: a G-->C transversion at 1245 position of the hOGG1 gene producing a Ser-->Cys substitution at the codon 326 (the Ser
74#79#gene588825#39#diseaseC0024623 16843501-0#74#79#gene5888 16843501-0#25#39#diseaseC0024623 associated_with RAD51,ge and repair study were correlated with the genotypes of common polymorphisms of the hOGG1 and RAD51 genes: a G-->C transversion at 1245 position of the hOGG1 gene producing a Ser-->Cys substitution at the codon 326 (the Ser
74#79#gene588825#39#diseaseC0699791 16843501-0#74#79#gene5888 16843501-0#25#39#diseaseC0699791 associated_with RAD51,ge and repair study were correlated with the genotypes of common polymorphisms of the hOGG1 and RAD51 genes: a G-->C transversion at 1245 position of the hOGG1 gene producing a Ser-->Cys substitution at the codon 326 (the Ser

tmVarCorpus

Id Subject Object Predicate Lexical cue
T1 982-1017 DNAMutation:g|SUB|G|1245|C denotes G-->C transversion at 1245 position
T2 1048-1087 ProteinMutation:p|SUB|S|326|C denotes Ser-->Cys substitution at the codon 326
T3 1093-1102 ProteinMutation:p|SUB|S|326|C denotes Ser326Cys
T4 1123-1157 DNAMutation:g|SUB|G|135|C denotes G-->C substitution at position 135
T5 1206-1211 DNAMutation:g|SUB|G|135|C denotes G135C
T6 1707-1712 DNAMutation:g|SUB|G|135|C denotes G135C
T7 1941-1951 ProteinMutation:p|SUB|S|1245|C denotes Ser1245Cys
T8 2142-2147 DNAMutation:g|SUB|G|135|C denotes G135C

DisGeNET

Id Subject Object Predicate Lexical cue
T0 1972-1977 gene:4968 denotes hOGG1
T1 1987-2001 disease:C0024623 denotes gastric cancer
T2 1972-1977 gene:4968 denotes hOGG1
T3 1987-2001 disease:C0699791 denotes gastric cancer
R1 T0 T1 associated_with hOGG1,gastric cancer
R2 T2 T3 associated_with hOGG1,gastric cancer