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c_corpus

Id Subject Object Predicate Lexical cue
T2 26-29 CHEBI:16768 denotes MSH
T6 26-29 D009074 denotes MSH
T7 26-29 D009074 denotes MSH
T8 26-30 PR:000010666 denotes MSH2
T9 26-30 PR:P25847 denotes MSH2
T10 26-30 PR:P43246 denotes MSH2
T11 26-30 P22711 denotes MSH2
T12 26-30 PR:P22711 denotes MSH2
T13 26-30 PR:P54275 denotes MSH2
T14 26-30 PR:O74773 denotes MSH2
T15 26-30 PR:P43247 denotes MSH2
T16 26-30 PR:Q553L4 denotes MSH2
T17 26-30 PR:O24617 denotes MSH2
T18 32-36 PR:Q9ZRV4 denotes MLH1
T19 32-36 PR:P38920 denotes MLH1
T20 32-36 PR:Q54KD8 denotes MLH1
T22 32-36 PR:Q9JK91 denotes MLH1
T23 32-36 PR:P97679 denotes MLH1
T24 32-36 PR:Q9P7W6 denotes MLH1
T25 32-36 PR:000010442 denotes MLH1
T26 32-36 PR:P40692 denotes MLH1
T21 32-36 CVCL_G669 denotes MLH1
T28 40-43 CHEBI:16768 denotes MSH
T32 40-43 D009074 denotes MSH
T33 40-43 D009074 denotes MSH
T34 40-44 PR:P52701 denotes MSH6
T35 40-44 PR:P54276 denotes MSH6
T36 40-44 PR:Q9VUM0 denotes MSH6
T37 40-44 PR:Q55GU9 denotes MSH6
T38 40-44 PR:O04716 denotes MSH6
T39 40-44 PR:Q03834 denotes MSH6
T40 40-44 PR:O74502 denotes MSH6
T41 40-44 PR:000010670 denotes MSH6
T42 122-139 D015179 denotes colorectal cancer
T43 122-139 D015179 denotes colorectal cancer
T44 154-172 C566739 denotes autosomal dominant
T45 173-180 D004194 denotes disease
T46 173-180 D004194 denotes disease
T47 239-254 GO:0006298 denotes mismatch repair
T50 256-259 P22897 denotes MMR
T51 256-259 PR:000002972 denotes MMR
T52 256-259 Q61830 denotes MMR
T49 256-259 CVCL_E779 denotes MMR
T48 256-259 GO:0006298 denotes MMR
T53 267-271 PR:Q9ZRV4 denotes MLH1
T54 267-271 PR:P38920 denotes MLH1
T55 267-271 PR:Q54KD8 denotes MLH1
T57 267-271 PR:Q9JK91 denotes MLH1
T58 267-271 PR:P97679 denotes MLH1
T59 267-271 PR:Q9P7W6 denotes MLH1
T60 267-271 PR:000010442 denotes MLH1
T61 267-271 PR:P40692 denotes MLH1
T56 267-271 CVCL_G669 denotes MLH1
T63 273-276 CHEBI:16768 denotes MSH
T67 273-276 D009074 denotes MSH
T68 273-276 D009074 denotes MSH
T69 273-277 PR:000010666 denotes MSH2
T70 273-277 PR:P25847 denotes MSH2
T71 273-277 PR:P43246 denotes MSH2
T72 273-277 P22711 denotes MSH2
T73 273-277 PR:P22711 denotes MSH2
T74 273-277 PR:P54275 denotes MSH2
T75 273-277 PR:O74773 denotes MSH2
T76 273-277 PR:P43247 denotes MSH2
T77 273-277 PR:Q553L4 denotes MSH2
T78 273-277 PR:O24617 denotes MSH2
T80 279-282 CHEBI:16768 denotes MSH
T84 279-282 D009074 denotes MSH
T85 279-282 D009074 denotes MSH
T86 279-283 PR:P52701 denotes MSH6
T87 279-283 PR:P54276 denotes MSH6
T88 279-283 PR:Q9VUM0 denotes MSH6
T89 279-283 PR:Q55GU9 denotes MSH6
T90 279-283 PR:O04716 denotes MSH6
T91 279-283 PR:Q03834 denotes MSH6
T92 279-283 PR:O74502 denotes MSH6
T93 279-283 PR:000010670 denotes MSH6
T94 285-288 CHEBI:53396 denotes PMS
T97 285-288 CHEBI:53430 denotes PMS
T99 285-288 CHEBI:8055 denotes PMS
T100 285-289 PR:P54279 denotes PMS2
T101 285-289 PR:F1NQJ3 denotes PMS2
T102 285-289 PR:P38920 denotes PMS2
T103 285-289 PR:000012914 denotes PMS2
T104 285-289 PR:P54278 denotes PMS2
T105 294-298 PR:F4JN26 denotes MLH3
T106 294-298 PR:Q12083 denotes MLH3
T107 294-298 PR:000010443 denotes MLH3
T108 294-298 PR:Q9UHC1 denotes MLH3
T110 374-378 SO:0001236 denotes base
T109 374-378 CHEBI:22695 denotes base
T111 522-525 Q41249 denotes PCR
T112 522-525 O66148 denotes PCR
T113 522-525 Q59987 denotes PCR
T114 522-525 Q01289 denotes PCR
T115 522-525 O80333 denotes PCR
T116 522-525 P15904 denotes PCR
T117 522-525 Q9SDT1 denotes PCR
T118 522-525 Q39617 denotes PCR
T121 649-652 P22897 denotes MMR
T122 649-652 PR:000002972 denotes MMR
T123 649-652 Q61830 denotes MMR
T120 649-652 CVCL_E779 denotes MMR
T119 649-652 GO:0006298 denotes MMR
T124 653-657 SO:0000704 denotes gene
T125 658-672 SO:1000008 denotes point mutation
T127 719-723 PR:Q9ZRV4 denotes MLH1
T128 719-723 PR:P38920 denotes MLH1
T129 719-723 PR:Q54KD8 denotes MLH1
T131 719-723 PR:Q9JK91 denotes MLH1
T132 719-723 PR:P97679 denotes MLH1
T133 719-723 PR:Q9P7W6 denotes MLH1
T134 719-723 PR:000010442 denotes MLH1
T135 719-723 PR:P40692 denotes MLH1
T130 719-723 CVCL_G669 denotes MLH1
T137 725-728 CHEBI:16768 denotes MSH
T141 725-728 D009074 denotes MSH
T142 725-728 D009074 denotes MSH
T143 725-729 PR:000010666 denotes MSH2
T144 725-729 PR:P25847 denotes MSH2
T145 725-729 PR:P43246 denotes MSH2
T146 725-729 P22711 denotes MSH2
T147 725-729 PR:P22711 denotes MSH2
T148 725-729 PR:P54275 denotes MSH2
T149 725-729 PR:O74773 denotes MSH2
T150 725-729 PR:P43247 denotes MSH2
T151 725-729 PR:Q553L4 denotes MSH2
T152 725-729 PR:O24617 denotes MSH2
T154 733-736 CHEBI:16768 denotes MSH
T158 733-736 D009074 denotes MSH
T159 733-736 D009074 denotes MSH
T160 733-737 PR:P52701 denotes MSH6
T161 733-737 PR:P54276 denotes MSH6
T162 733-737 PR:Q9VUM0 denotes MSH6
T163 733-737 PR:Q55GU9 denotes MSH6
T164 733-737 PR:O04716 denotes MSH6
T165 733-737 PR:Q03834 denotes MSH6
T166 733-737 PR:O74502 denotes MSH6
T167 733-737 PR:000010670 denotes MSH6
T168 772-786 SO:1000008 denotes point mutation
T170 808-814 UBERON:0000479 denotes tissue
T171 815-818 GO:0005574 denotes DNA
T173 815-818 SO:0000352 denotes DNA
T172 815-818 CHEBI:16991 denotes DNA
T174 815-818 D004247 denotes DNA
T175 826-843 D015179 denotes colorectal cancer
T176 826-843 D015179 denotes colorectal cancer
T177 845-848 PR:Q8L925 denotes CRC
T179 845-848 PR:Q96318 denotes CRC
T180 845-848 PR:P29413 denotes CRC
T181 845-848 Q719L8 denotes CRC
T178 845-848 D015179 denotes CRC
T182 891-896 SO:0000051 denotes probe
T183 891-896 CHEBI:50406 denotes probe
T184 912-916 PR:000023112 denotes MLPA
T185 912-916 PR:P69776 denotes MLPA
T188 961-964 SO:0002045 denotes pre
T187 961-964 PR:Q8LLD0 denotes pre
T189 961-964 UBERON:0001782 denotes pre
T186 961-964 GO:0003904 denotes pre
T190 990-993 CHEBI:32644 denotes met
T191 1054-1060 D009369 denotes tumors
T192 1054-1060 D009369 denotes tumors
T193 1076-1090 SO:0000289 denotes microsatellite
T194 1076-1102 D053842 denotes microsatellite instability
T195 1076-1102 D053842 denotes microsatellite instability
T196 1104-1107 PR:000006870 denotes MSI
T197 1104-1107 PR:P70245 denotes MSI
T198 1147-1151 PR:Q9ZRV4 denotes MLH1
T199 1147-1151 PR:P38920 denotes MLH1
T200 1147-1151 PR:Q54KD8 denotes MLH1
T202 1147-1151 PR:Q9JK91 denotes MLH1
T203 1147-1151 PR:P97679 denotes MLH1
T204 1147-1151 PR:Q9P7W6 denotes MLH1
T205 1147-1151 PR:000010442 denotes MLH1
T206 1147-1151 PR:P40692 denotes MLH1
T201 1147-1151 CVCL_G669 denotes MLH1
T208 1153-1156 CHEBI:16768 denotes MSH
T212 1153-1156 D009074 denotes MSH
T213 1153-1156 D009074 denotes MSH
T214 1153-1157 PR:000010666 denotes MSH2
T215 1153-1157 PR:P25847 denotes MSH2
T216 1153-1157 PR:P43246 denotes MSH2
T217 1153-1157 P22711 denotes MSH2
T218 1153-1157 PR:P22711 denotes MSH2
T219 1153-1157 PR:P54275 denotes MSH2
T220 1153-1157 PR:O74773 denotes MSH2
T221 1153-1157 PR:P43247 denotes MSH2
T222 1153-1157 PR:Q553L4 denotes MSH2
T223 1153-1157 PR:O24617 denotes MSH2
T225 1161-1164 CHEBI:16768 denotes MSH
T229 1161-1164 D009074 denotes MSH
T230 1161-1164 D009074 denotes MSH
T231 1161-1165 PR:P52701 denotes MSH6
T232 1161-1165 PR:P54276 denotes MSH6
T233 1161-1165 PR:Q9VUM0 denotes MSH6
T234 1161-1165 PR:Q55GU9 denotes MSH6
T235 1161-1165 PR:O04716 denotes MSH6
T236 1161-1165 PR:Q03834 denotes MSH6
T237 1161-1165 PR:O74502 denotes MSH6
T238 1161-1165 PR:000010670 denotes MSH6
T239 1166-1174 CHEBI:36080 denotes proteins
T240 1176-1179 Q41249 denotes PCR
T241 1176-1179 O66148 denotes PCR
T242 1176-1179 Q59987 denotes PCR
T243 1176-1179 Q01289 denotes PCR
T244 1176-1179 O80333 denotes PCR
T245 1176-1179 P15904 denotes PCR
T246 1176-1179 Q9SDT1 denotes PCR
T247 1176-1179 Q39617 denotes PCR
T248 1245-1248 GO:0006298 denotes MMR
T250 1245-1248 P22897 denotes MMR
T251 1245-1248 PR:000002972 denotes MMR
T252 1245-1248 Q61830 denotes MMR
T249 1245-1248 CVCL_E779 denotes MMR
T253 1249-1253 SO:0000704 denotes gene
T258 1261-1268 SO:0000104 denotes protein
T255 1261-1268 CHEBI:36080 denotes protein
T256 1261-1268 CHEBI:11122 denotes protein
T257 1261-1268 PR:000000001 denotes protein
T254 1261-1268 GO:0003675 denotes protein
T259 1301-1306 D009369 denotes tumor
T260 1301-1306 D009369 denotes tumor
T261 1307-1313 UBERON:0000479 denotes tissue
T262 1354-1368 SO:1000008 denotes point mutation
T264 1416-1430 SO:1000008 denotes point mutation
T266 1434-1438 PR:Q9ZRV4 denotes MLH1
T267 1434-1438 PR:P38920 denotes MLH1
T268 1434-1438 PR:Q54KD8 denotes MLH1
T270 1434-1438 PR:Q9JK91 denotes MLH1
T271 1434-1438 PR:P97679 denotes MLH1
T272 1434-1438 PR:Q9P7W6 denotes MLH1
T273 1434-1438 PR:000010442 denotes MLH1
T274 1434-1438 PR:P40692 denotes MLH1
T269 1434-1438 CVCL_G669 denotes MLH1
T277 1449-1452 CHEBI:16768 denotes MSH
T281 1449-1452 D009074 denotes MSH
T282 1449-1452 D009074 denotes MSH
T283 1449-1453 PR:000010666 denotes MSH2
T284 1449-1453 PR:P25847 denotes MSH2
T285 1449-1453 PR:P43246 denotes MSH2
T286 1449-1453 P22711 denotes MSH2
T287 1449-1453 PR:P22711 denotes MSH2
T288 1449-1453 PR:P54275 denotes MSH2
T289 1449-1453 PR:O74773 denotes MSH2
T290 1449-1453 PR:P43247 denotes MSH2
T291 1449-1453 PR:Q553L4 denotes MSH2
T292 1449-1453 PR:O24617 denotes MSH2
T297 1464-1467 CHEBI:16768 denotes MSH
T301 1464-1467 D009074 denotes MSH
T302 1464-1467 D009074 denotes MSH
T303 1464-1468 PR:P52701 denotes MSH6
T304 1464-1468 PR:P54276 denotes MSH6
T305 1464-1468 PR:Q9VUM0 denotes MSH6
T306 1464-1468 PR:Q55GU9 denotes MSH6
T307 1464-1468 PR:O04716 denotes MSH6
T308 1464-1468 PR:Q03834 denotes MSH6
T309 1464-1468 PR:O74502 denotes MSH6
T310 1464-1468 PR:000010670 denotes MSH6
T312 1523-1530 SO:0001147 denotes variant
T313 1534-1538 PR:Q9ZRV4 denotes MLH1
T314 1534-1538 PR:P38920 denotes MLH1
T315 1534-1538 PR:Q54KD8 denotes MLH1
T317 1534-1538 PR:Q9JK91 denotes MLH1
T318 1534-1538 PR:P97679 denotes MLH1
T319 1534-1538 PR:Q9P7W6 denotes MLH1
T320 1534-1538 PR:000010442 denotes MLH1
T321 1534-1538 PR:P40692 denotes MLH1
T316 1534-1538 CVCL_G669 denotes MLH1
T323 1548-1551 CHEBI:16768 denotes MSH
T327 1548-1551 D009074 denotes MSH
T328 1548-1551 D009074 denotes MSH
T329 1548-1552 PR:000010666 denotes MSH2
T330 1548-1552 PR:P25847 denotes MSH2
T331 1548-1552 PR:P43246 denotes MSH2
T332 1548-1552 P22711 denotes MSH2
T333 1548-1552 PR:P22711 denotes MSH2
T334 1548-1552 PR:P54275 denotes MSH2
T335 1548-1552 PR:O74773 denotes MSH2
T336 1548-1552 PR:P43247 denotes MSH2
T337 1548-1552 PR:Q553L4 denotes MSH2
T338 1548-1552 PR:O24617 denotes MSH2
T340 1562-1565 CHEBI:16768 denotes MSH
T344 1562-1565 D009074 denotes MSH
T345 1562-1565 D009074 denotes MSH
T346 1562-1566 PR:P52701 denotes MSH6
T347 1562-1566 PR:P54276 denotes MSH6
T348 1562-1566 PR:Q9VUM0 denotes MSH6
T349 1562-1566 PR:Q55GU9 denotes MSH6
T350 1562-1566 PR:O04716 denotes MSH6
T351 1562-1566 PR:Q03834 denotes MSH6
T352 1562-1566 PR:O74502 denotes MSH6
T353 1562-1566 PR:000010670 denotes MSH6
T354 1642-1646 PR:P33696 denotes exon
T355 1642-1646 SO:0000147 denotes exon
T356 1692-1695 G0R947 denotes EX1
T357 1692-1695 P36218 denotes EX1
T358 1692-1695 PR:Q93YW0 denotes EX1
T359 1698-1701 PR:Q9VIF5 denotes del
T360 1698-1701 CVCL_1170 denotes del
T361 1698-1701 UBERON:2000711 denotes del
T362 1705-1709 PR:Q9ZRV4 denotes MLH1
T363 1705-1709 PR:P38920 denotes MLH1
T364 1705-1709 PR:Q54KD8 denotes MLH1
T366 1705-1709 PR:Q9JK91 denotes MLH1
T367 1705-1709 PR:P97679 denotes MLH1
T368 1705-1709 PR:Q9P7W6 denotes MLH1
T369 1705-1709 PR:000010442 denotes MLH1
T370 1705-1709 PR:P40692 denotes MLH1
T365 1705-1709 CVCL_G669 denotes MLH1
T373 1867-1870 P22897 denotes MMR
T374 1867-1870 PR:000002972 denotes MMR
T375 1867-1870 Q61830 denotes MMR
T372 1867-1870 CVCL_E779 denotes MMR
T371 1867-1870 GO:0006298 denotes MMR
T378 1977-1980 P22897 denotes MMR
T379 1977-1980 PR:000002972 denotes MMR
T380 1977-1980 Q61830 denotes MMR
T377 1977-1980 CVCL_E779 denotes MMR
T376 1977-1980 GO:0006298 denotes MMR

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 133-139 HP_0002664 denotes cancer
T2 154-172 HP_0000006 denotes autosomal dominant
T3 491-503 HP_0009609 denotes duplications
T4 837-843 HP_0002664 denotes cancer
T5 1054-1060 HP_0002664 denotes tumors
T6 1301-1306 HP_0002664 denotes tumor

UseCases_ArguminSci_Discourse

Id Subject Object Predicate Lexical cue
T1 0-97 DRI_Background denotes Genomic rearrangements in MSH2, MLH1 or MSH6 are rare in HNPCC patients carrying point mutations.
T2 98-299 DRI_Background denotes Hereditary nonpolyposis colorectal cancer (HNPCC) is an autosomal dominant disease with high penetrance, caused by germline mutations in the mismatch repair (MMR) genes MLH1, MSH2, MSH6, PMS2 and MLH3.
T3 300-425 DRI_Approach denotes Most reported pathogenic mutations are point mutations, comprising single base substitutions, small insertions and deletions.
T4 426-673 DRI_Background denotes In addition, genomic rearrangements, such as large deletions and duplications not detectable by PCR and Sanger sequencing, have been identified in a significant proportion of HNPCC families, which do not carry a pathogenic MMR gene point mutation.
T5 674-927 DRI_Background denotes To clarify whether genomic rearrangements in MLH1, MSH2 or MSH6 also occur in patients carrying a point mutation, we subjected normal tissue DNA of 137 colorectal cancer (CRC) patients to multiplex ligation-dependent probe amplification (MLPA) analysis.
T6 928-1175 DRI_Outcome denotes Patients fulfilled the following pre-requisites: all patients met at least one criterion of the Bethesda guidelines and their tumors exhibited high microsatellite instability (MSI-H) and/or showed loss of expression of MLH1, MSH2 or MSH6 proteins.
T7 1176-1583 DRI_Background denotes PCR amplification and Sanger sequencing of all exons of at least one MMR gene, whose protein expression had been lost in the tumor tissue, identified 52 index patients without a point mutation (Group 1), 71 index patients with a pathogenic point mutation in MLH1 (n=38) or MSH2 (n=22) or MSH6 (n=11) (Group 2) and 14 patients with an unclassified variant in MLH1 (n=9) or MSH2 (n=3) or MSH6 (n=2) (Group 3).
T8 1584-1663 DRI_Background denotes In 13 of 52 patients of group 1 deletions of at least one exon were identified.
T9 1664-1720 DRI_Background denotes In addition, in group 3 one EX1_15del in MLH1 was found.
T10 1721-1781 DRI_Background denotes No genomic rearrangement was identified in group 2 patients.
T11 1782-1895 DRI_Background denotes Genomic rearrangements represent a significant proportion of pathogenic mutations of MMR genes in HNPCC patients.
T12 1896-1987 DRI_Background denotes However, genomic rearrangements are rare in patients carrying point mutations in MMR genes.
T13 1988-2101 DRI_Background denotes These findings suggest the use of genomic rearrangement tests in addition to Sanger sequencing in HNPCC patients.

PubMed_ArguminSci

Id Subject Object Predicate Lexical cue
T1 98-299 DRI_Background denotes Hereditary nonpolyposis colorectal cancer (HNPCC) is an autosomal dominant disease with high penetrance, caused by germline mutations in the mismatch repair (MMR) genes MLH1, MSH2, MSH6, PMS2 and MLH3.
T2 300-425 DRI_Approach denotes Most reported pathogenic mutations are point mutations, comprising single base substitutions, small insertions and deletions.
T3 426-673 DRI_Background denotes In addition, genomic rearrangements, such as large deletions and duplications not detectable by PCR and Sanger sequencing, have been identified in a significant proportion of HNPCC families, which do not carry a pathogenic MMR gene point mutation.
T4 674-927 DRI_Background denotes To clarify whether genomic rearrangements in MLH1, MSH2 or MSH6 also occur in patients carrying a point mutation, we subjected normal tissue DNA of 137 colorectal cancer (CRC) patients to multiplex ligation-dependent probe amplification (MLPA) analysis.
T5 928-1175 DRI_Outcome denotes Patients fulfilled the following pre-requisites: all patients met at least one criterion of the Bethesda guidelines and their tumors exhibited high microsatellite instability (MSI-H) and/or showed loss of expression of MLH1, MSH2 or MSH6 proteins.
T6 1176-1583 DRI_Background denotes PCR amplification and Sanger sequencing of all exons of at least one MMR gene, whose protein expression had been lost in the tumor tissue, identified 52 index patients without a point mutation (Group 1), 71 index patients with a pathogenic point mutation in MLH1 (n=38) or MSH2 (n=22) or MSH6 (n=11) (Group 2) and 14 patients with an unclassified variant in MLH1 (n=9) or MSH2 (n=3) or MSH6 (n=2) (Group 3).
T7 1584-1663 DRI_Background denotes In 13 of 52 patients of group 1 deletions of at least one exon were identified.
T8 1664-1720 DRI_Background denotes In addition, in group 3 one EX1_15del in MLH1 was found.
T9 1721-1781 DRI_Background denotes No genomic rearrangement was identified in group 2 patients.
T10 1782-1895 DRI_Background denotes Genomic rearrangements represent a significant proportion of pathogenic mutations of MMR genes in HNPCC patients.
T11 1896-1987 DRI_Background denotes However, genomic rearrangements are rare in patients carrying point mutations in MMR genes.
T12 1988-2101 DRI_Background denotes These findings suggest the use of genomic rearrangement tests in addition to Sanger sequencing in HNPCC patients.

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
16837128-0#40#44#gene2956 40-44 gene2956 denotes MSH6
16837128-0#57#62#diseaseC1333990 57-62 diseaseC1333990 denotes HNPCC
16837128-1#169#173#gene4292 267-271 gene4292 denotes MLH1
16837128-1#175#179#gene4436 273-277 gene4436 denotes MSH2
16837128-1#187#191#gene5395 285-289 gene5395 denotes PMS2
16837128-1#196#200#gene27030 294-298 gene27030 denotes MLH3
16837128-1#0#41#diseaseC1333990 98-139 diseaseC1333990 denotes Hereditary nonpolyposis colorectal cancer
16837128-1#43#48#diseaseC1333990 141-146 diseaseC1333990 denotes HNPCC
16837128-1#0#41#diseaseC1333990 98-139 diseaseC1333990 denotes Hereditary nonpolyposis colorectal cancer
16837128-1#43#48#diseaseC1333990 141-146 diseaseC1333990 denotes HNPCC
16837128-10#85#88#gene4360 1867-1870 gene4360 denotes MMR
16837128-10#98#103#diseaseC1333990 1880-1885 diseaseC1333990 denotes HNPCC
40#44#gene295657#62#diseaseC1333990 16837128-0#40#44#gene2956 16837128-0#57#62#diseaseC1333990 associated_with MSH6,HNPCC
169#173#gene42920#41#diseaseC1333990 16837128-1#169#173#gene4292 16837128-1#0#41#diseaseC1333990 associated_with MLH1,Hereditary nonpolyposis colorectal cancer
169#173#gene429243#48#diseaseC1333990 16837128-1#169#173#gene4292 16837128-1#43#48#diseaseC1333990 associated_with MLH1,HNPCC
169#173#gene42920#41#diseaseC1333990 16837128-1#169#173#gene4292 16837128-1#0#41#diseaseC1333990 associated_with MLH1,Hereditary nonpolyposis colorectal cancer
169#173#gene429243#48#diseaseC1333990 16837128-1#169#173#gene4292 16837128-1#43#48#diseaseC1333990 associated_with MLH1,HNPCC
175#179#gene44360#41#diseaseC1333990 16837128-1#175#179#gene4436 16837128-1#0#41#diseaseC1333990 associated_with MSH2,Hereditary nonpolyposis colorectal cancer
175#179#gene443643#48#diseaseC1333990 16837128-1#175#179#gene4436 16837128-1#43#48#diseaseC1333990 associated_with MSH2,HNPCC
175#179#gene44360#41#diseaseC1333990 16837128-1#175#179#gene4436 16837128-1#0#41#diseaseC1333990 associated_with MSH2,Hereditary nonpolyposis colorectal cancer
175#179#gene443643#48#diseaseC1333990 16837128-1#175#179#gene4436 16837128-1#43#48#diseaseC1333990 associated_with MSH2,HNPCC
187#191#gene53950#41#diseaseC1333990 16837128-1#187#191#gene5395 16837128-1#0#41#diseaseC1333990 associated_with PMS2,Hereditary nonpolyposis colorectal cancer
187#191#gene539543#48#diseaseC1333990 16837128-1#187#191#gene5395 16837128-1#43#48#diseaseC1333990 associated_with PMS2,HNPCC
187#191#gene53950#41#diseaseC1333990 16837128-1#187#191#gene5395 16837128-1#0#41#diseaseC1333990 associated_with PMS2,Hereditary nonpolyposis colorectal cancer
187#191#gene539543#48#diseaseC1333990 16837128-1#187#191#gene5395 16837128-1#43#48#diseaseC1333990 associated_with PMS2,HNPCC
196#200#gene270300#41#diseaseC1333990 16837128-1#196#200#gene27030 16837128-1#0#41#diseaseC1333990 associated_with MLH3,Hereditary nonpolyposis colorectal cancer
196#200#gene2703043#48#diseaseC1333990 16837128-1#196#200#gene27030 16837128-1#43#48#diseaseC1333990 associated_with MLH3,HNPCC
196#200#gene270300#41#diseaseC1333990 16837128-1#196#200#gene27030 16837128-1#0#41#diseaseC1333990 associated_with MLH3,Hereditary nonpolyposis colorectal cancer
196#200#gene2703043#48#diseaseC1333990 16837128-1#196#200#gene27030 16837128-1#43#48#diseaseC1333990 associated_with MLH3,HNPCC
85#88#gene436098#103#diseaseC1333990 16837128-10#85#88#gene4360 16837128-10#98#103#diseaseC1333990 associated_with MMR,HNPCC

DisGeNET

Id Subject Object Predicate Lexical cue
T0 256-259 gene:4360 denotes MMR
T1 98-139 disease:C1333990 denotes Hereditary nonpolyposis colorectal cancer
T2 256-259 gene:4360 denotes MMR
T3 141-146 disease:C1333990 denotes HNPCC
T4 267-271 gene:4292 denotes MLH1
T5 98-139 disease:C1333990 denotes Hereditary nonpolyposis colorectal cancer
T6 267-271 gene:4292 denotes MLH1
T7 141-146 disease:C1333990 denotes HNPCC
T8 273-277 gene:4436 denotes MSH2
T9 98-139 disease:C1333990 denotes Hereditary nonpolyposis colorectal cancer
T10 279-283 gene:2956 denotes MSH6
T11 98-139 disease:C1333990 denotes Hereditary nonpolyposis colorectal cancer
T12 285-289 gene:5395 denotes PMS2
T13 98-139 disease:C1333990 denotes Hereditary nonpolyposis colorectal cancer
T14 285-289 gene:5395 denotes PMS2
T15 141-146 disease:C1333990 denotes HNPCC
T16 294-298 gene:27030 denotes MLH3
T17 98-139 disease:C1333990 denotes Hereditary nonpolyposis colorectal cancer
T18 294-298 gene:27030 denotes MLH3
T19 141-146 disease:C1333990 denotes HNPCC
R1 T0 T1 associated_with MMR,Hereditary nonpolyposis colorectal cancer
R2 T2 T3 associated_with MMR,HNPCC
R3 T4 T5 associated_with MLH1,Hereditary nonpolyposis colorectal cancer
R4 T6 T7 associated_with MLH1,HNPCC
R5 T8 T9 associated_with MSH2,Hereditary nonpolyposis colorectal cancer
R6 T10 T11 associated_with MSH6,Hereditary nonpolyposis colorectal cancer
R7 T12 T13 associated_with PMS2,Hereditary nonpolyposis colorectal cancer
R8 T14 T15 associated_with PMS2,HNPCC
R9 T16 T17 associated_with MLH3,Hereditary nonpolyposis colorectal cancer
R10 T18 T19 associated_with MLH3,HNPCC