PMC:1860061 / 11837-13198 JSONTXT 5 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function

Id Subject Object Predicate Lexical cue
T7423 0-6 NNP denotes Lander
T7425 7-10 CC denotes and
T7426 11-19 NNP denotes Botstein
T7427 20-21 -LRB- denotes [
T7428 21-23 CD denotes 26
T7429 23-24 -RRB- denotes ]
T7424 25-34 VBD denotes suggested
T7430 35-36 DT denotes a
T7432 37-40 NN denotes LOD
T7431 41-46 NN denotes score
T7433 47-49 IN denotes of
T7434 50-57 IN denotes between
T7435 58-59 CD denotes 2
T7436 60-63 CC denotes and
T7437 64-65 CD denotes 3
T7438 66-68 TO denotes to
T7439 69-75 VB denotes ensure
T7440 76-78 DT denotes an
T7442 79-86 JJ denotes overall
T7443 87-92 JJ denotes false
T7444 93-101 JJ denotes positive
T7441 102-106 NN denotes rate
T7445 107-109 IN denotes of
T7446 110-111 CD denotes 5
T7447 111-112 NN denotes %
T7448 112-114 , denotes ,
T7449 114-119 WDT denotes which
T7450 120-125 VBZ denotes means
T7451 126-130 IN denotes that
T7453 131-136 VBG denotes using
T7454 137-138 DT denotes a
T7456 139-144 JJR denotes lower
T7457 145-154 NN denotes threshold
T7455 155-160 NN denotes value
T7458 161-165 MD denotes will
T7452 166-173 VB denotes prevent
T7459 174-179 JJ denotes false
T7460 180-188 JJ denotes negative
T7461 189-192 NNS denotes QTL
T7462 193-195 IN denotes at
T7463 196-199 DT denotes the
T7464 200-207 NN denotes expense
T7465 208-210 IN denotes of
T7466 211-221 VBG denotes increasing
T7467 222-227 JJ denotes false
T7468 228-236 JJ denotes positive
T7469 237-240 NNS denotes QTL
T7470 240-241 . denotes .
T7471 241-417 sentence denotes Being aware of this, we examined these genomic regions to search whether they, or their syntenic genomic regions on the human genome, have been previously linked to arthritis.
T7472 242-247 VBG denotes Being
T7474 248-253 JJ denotes aware
T7475 254-256 IN denotes of
T7476 257-261 DT denotes this
T7477 261-263 , denotes ,
T7478 263-265 PRP denotes we
T7473 266-274 VBD denotes examined
T7479 275-280 DT denotes these
T7481 281-288 JJ denotes genomic
T7480 289-296 NNS denotes regions
T7482 297-299 TO denotes to
T7483 300-306 VB denotes search
T7484 307-314 IN denotes whether
T7486 315-319 PRP denotes they
T7487 319-321 , denotes ,
T7488 321-323 CC denotes or
T7489 324-329 PRP$ denotes their
T7491 330-338 JJ denotes syntenic
T7492 339-346 JJ denotes genomic
T7490 347-354 NNS denotes regions
T7493 355-357 IN denotes on
T7494 358-361 DT denotes the
T7496 362-367 JJ denotes human
T7495 368-374 NN denotes genome
T7497 374-376 , denotes ,
T7498 376-380 VBP denotes have
T7499 381-385 VBN denotes been
T7500 386-396 RB denotes previously
T7485 397-403 VBN denotes linked
T7501 404-406 IN denotes to
T7502 407-416 NN denotes arthritis
T7503 416-417 . denotes .
T7504 417-512 sentence denotes Four small-effect QTL overlapped with arthritis QTL on the mouse genome identified previously.
T7505 418-422 CD denotes Four
T7507 423-428 JJ denotes small
T7509 428-429 HYPH denotes -
T7508 429-435 NN denotes effect
T7506 436-439 NNS denotes QTL
T7510 440-450 VBD denotes overlapped
T7511 451-455 IN denotes with
T7512 456-465 NN denotes arthritis
T7513 466-469 NNS denotes QTL
T7514 470-472 IN denotes on
T7515 473-476 DT denotes the
T7517 477-482 NN denotes mouse
T7516 483-489 NN denotes genome
T7518 490-500 VBN denotes identified
T7519 501-511 RB denotes previously
T7520 511-512 . denotes .
T7521 512-623 sentence denotes Locus 1 and 2 overlap with Cia13 and Cia14, which control severity of CIA in (DBA/1 × BALB/C) F2 progeny [27].
T7522 513-518 NN denotes Locus
T7523 519-520 CD denotes 1
T7525 521-524 CC denotes and
T7526 525-526 CD denotes 2
T7524 527-534 VBP denotes overlap
T7527 535-539 IN denotes with
T7528 540-545 NN denotes Cia13
T7529 546-549 CC denotes and
T7530 550-555 NN denotes Cia14
T7531 555-557 , denotes ,
T7532 557-562 WDT denotes which
T7533 563-570 VBP denotes control
T7534 571-579 NN denotes severity
T7535 580-582 IN denotes of
T7536 583-586 NN denotes CIA
T7537 587-589 IN denotes in
T7538 590-591 -LRB- denotes (
T7539 591-594 NN denotes DBA
T7541 594-595 HYPH denotes /
T7542 595-596 CD denotes 1
T7543 597-598 SYM denotes ×
T7544 599-603 NN denotes BALB
T7546 603-604 HYPH denotes /
T7545 604-605 NN denotes C
T7547 605-606 -RRB- denotes )
T7548 607-609 NN denotes F2
T7540 610-617 NN denotes progeny
T7549 618-619 -LRB- denotes [
T7550 619-621 CD denotes 27
T7551 621-622 -RRB- denotes ]
T7552 622-623 . denotes .
T7553 623-733 sentence denotes Locus 5 located on chromosome 10 overlaps with Cia8, which was identified in (DBA/1 × B10.Q) F2 progeny [28].
T7554 624-629 NN denotes Locus
T7556 630-631 CD denotes 5
T7557 632-639 VBN denotes located
T7558 640-642 IN denotes on
T7559 643-653 NN denotes chromosome
T7560 654-656 CD denotes 10
T7555 657-665 VBZ denotes overlaps
T7561 666-670 IN denotes with
T7562 671-675 NN denotes Cia8
T7563 675-677 , denotes ,
T7564 677-682 WDT denotes which
T7566 683-686 VBD denotes was
T7565 687-697 VBN denotes identified
T7567 698-700 IN denotes in
T7568 701-702 -LRB- denotes (
T7569 702-705 NN denotes DBA
T7571 705-706 HYPH denotes /
T7572 706-707 CD denotes 1
T7573 708-709 SYM denotes ×
T7574 710-715 NN denotes B10.Q
T7575 715-716 -RRB- denotes )
T7576 717-719 NN denotes F2
T7570 720-727 NN denotes progeny
T7577 728-729 -LRB- denotes [
T7578 729-731 CD denotes 28
T7579 731-732 -RRB- denotes ]
T7580 732-733 . denotes .
T7581 733-889 sentence denotes Locus 6 overlaps with Pgia7, which controls susceptibility to proteoglycan-induced arthritis (PGIA) and was identified in (BALB/C × DBA/2) F2 progeny [29].
T7582 734-739 NN denotes Locus
T7584 740-741 CD denotes 6
T7583 742-750 VBZ denotes overlaps
T7585 751-755 IN denotes with
T7586 756-761 NN denotes Pgia7
T7587 761-763 , denotes ,
T7588 763-768 WDT denotes which
T7589 769-777 VBZ denotes controls
T7590 778-792 NN denotes susceptibility
T7591 793-795 IN denotes to
T7592 796-808 NN denotes proteoglycan
T7594 808-809 HYPH denotes -
T7593 809-816 VBN denotes induced
T7595 817-826 NN denotes arthritis
T7596 827-828 -LRB- denotes (
T7597 828-832 NN denotes PGIA
T7598 832-833 -RRB- denotes )
T7599 834-837 CC denotes and
T7600 838-841 VBD denotes was
T7601 842-852 VBN denotes identified
T7602 853-855 IN denotes in
T7603 856-857 -LRB- denotes (
T7605 857-861 NN denotes BALB
T7606 861-862 HYPH denotes /
T7604 862-863 NN denotes C
T7608 864-865 SYM denotes ×
T7609 866-869 NN denotes DBA
T7610 869-870 HYPH denotes /
T7611 870-871 CD denotes 2
T7612 871-872 -RRB- denotes )
T7613 873-875 NN denotes F2
T7607 876-883 NN denotes progeny
T7614 884-885 -LRB- denotes [
T7615 885-887 CD denotes 29
T7616 887-888 -RRB- denotes ]
T7617 888-889 . denotes .
T7618 889-1002 sentence denotes The syntenic genomic regions of five small-effect QTL on the human genome have been reported to be linked to RA.
T7619 890-893 DT denotes The
T7621 894-902 JJ denotes syntenic
T7622 903-910 JJ denotes genomic
T7620 911-918 NNS denotes regions
T7624 919-921 IN denotes of
T7625 922-926 CD denotes five
T7627 927-932 JJ denotes small
T7629 932-933 HYPH denotes -
T7628 933-939 NN denotes effect
T7626 940-943 NNS denotes QTL
T7630 944-946 IN denotes on
T7631 947-950 DT denotes the
T7633 951-956 JJ denotes human
T7632 957-963 NN denotes genome
T7634 964-968 VBP denotes have
T7635 969-973 VBN denotes been
T7623 974-982 VBN denotes reported
T7636 983-985 TO denotes to
T7638 986-988 VB denotes be
T7637 989-995 VBN denotes linked
T7639 996-998 IN denotes to
T7640 999-1001 NN denotes RA
T7641 1001-1002 . denotes .
T7642 1002-1361 sentence denotes These are genomic regions 22q11 and 12p13-q24 on chromosome 22 and 12 (the counterparts of locus 2), 12p13-pter on chromosome 12 (the counterpart of locus 3), 21q22-qter and 10q22-23 on chromosome 21 and 10 (the counterparts of locus 5), 17q21-25 on chromosome 17 (the counterpart of locus 6) and 3q29-qter on chromosome 3 (the counterpart of locus 7) [2,4].
T7643 1003-1008 DT denotes These
T7644 1009-1012 VBP denotes are
T7645 1013-1020 JJ denotes genomic
T7646 1021-1028 NNS denotes regions
T7647 1029-1034 NN denotes 22q11
T7648 1035-1038 CC denotes and
T7649 1039-1044 NN denotes 12p13
T7651 1044-1045 HYPH denotes -
T7650 1045-1048 NN denotes q24
T7652 1049-1051 IN denotes on
T7653 1052-1062 NN denotes chromosome
T7654 1063-1065 CD denotes 22
T7655 1066-1069 CC denotes and
T7656 1070-1072 CD denotes 12
T7657 1073-1074 -LRB- denotes (
T7659 1074-1077 DT denotes the
T7658 1078-1090 NNS denotes counterparts
T7660 1091-1093 IN denotes of
T7661 1094-1099 NN denotes locus
T7662 1100-1101 CD denotes 2
T7663 1101-1102 -RRB- denotes )
T7664 1102-1104 , denotes ,
T7665 1104-1109 NN denotes 12p13
T7667 1109-1110 HYPH denotes -
T7666 1110-1114 NN denotes pter
T7668 1115-1117 IN denotes on
T7669 1118-1128 NN denotes chromosome
T7670 1129-1131 CD denotes 12
T7671 1132-1133 -LRB- denotes (
T7673 1133-1136 DT denotes the
T7672 1137-1148 NN denotes counterpart
T7674 1149-1151 IN denotes of
T7675 1152-1157 NN denotes locus
T7676 1158-1159 CD denotes 3
T7677 1159-1160 -RRB- denotes )
T7678 1160-1162 , denotes ,
T7679 1162-1167 NN denotes 21q22
T7681 1167-1168 HYPH denotes -
T7680 1168-1172 NN denotes qter
T7682 1173-1176 CC denotes and
T7683 1177-1182 NN denotes 10q22
T7684 1182-1183 HYPH denotes -
T7685 1183-1185 CD denotes 23
T7686 1186-1188 IN denotes on
T7687 1189-1199 NN denotes chromosome
T7688 1200-1202 CD denotes 21
T7689 1203-1206 CC denotes and
T7690 1207-1209 CD denotes 10
T7691 1210-1211 -LRB- denotes (
T7693 1211-1214 DT denotes the
T7692 1215-1227 NNS denotes counterparts
T7694 1228-1230 IN denotes of
T7695 1231-1236 NN denotes locus
T7696 1237-1238 CD denotes 5
T7697 1238-1239 -RRB- denotes )
T7698 1239-1241 , denotes ,
T7699 1241-1246 NN denotes 17q21
T7700 1246-1247 HYPH denotes -
T7701 1247-1249 CD denotes 25
T7702 1250-1252 IN denotes on
T7703 1253-1263 NN denotes chromosome
T7704 1264-1266 CD denotes 17
T7705 1267-1268 -LRB- denotes (
T7707 1268-1271 DT denotes the
T7706 1272-1283 NN denotes counterpart
T7708 1284-1286 IN denotes of
T7709 1287-1292 NN denotes locus
T7710 1293-1294 CD denotes 6
T7711 1294-1295 -RRB- denotes )
T7712 1296-1299 CC denotes and
T7713 1300-1304 NN denotes 3q29
T7715 1304-1305 HYPH denotes -
T7714 1305-1309 NN denotes qter
T7716 1310-1312 IN denotes on
T7717 1313-1323 NN denotes chromosome
T7718 1324-1325 CD denotes 3
T7719 1326-1327 -LRB- denotes (
T7721 1327-1330 DT denotes the
T7720 1331-1342 NN denotes counterpart
T7722 1343-1345 IN denotes of
T7723 1346-1351 NN denotes locus
T7724 1352-1353 CD denotes 7
T7725 1353-1354 -RRB- denotes )
T7726 1355-1356 -LRB- denotes [
T7728 1356-1357 CD denotes 2
T7729 1357-1358 , denotes ,
T7727 1358-1359 CD denotes 4
T7730 1359-1360 -RRB- denotes ]
T7731 1360-1361 . denotes .
R2147 T7423 T7424 nsubj Lander,suggested
R2148 T7425 T7423 cc and,Lander
R2149 T7426 T7423 conj Botstein,Lander
R2150 T7427 T7428 punct [,26
R2151 T7428 T7426 parataxis 26,Botstein
R2152 T7429 T7428 punct ],26
R2153 T7430 T7431 det a,score
R2154 T7431 T7424 dobj score,suggested
R2155 T7432 T7431 compound LOD,score
R2156 T7433 T7431 prep of,score
R2157 T7434 T7435 quantmod between,2
R2158 T7435 T7433 pobj 2,of
R2159 T7436 T7435 cc and,2
R2160 T7437 T7435 conj 3,2
R2161 T7438 T7439 aux to,ensure
R2162 T7439 T7424 advcl ensure,suggested
R2163 T7440 T7441 det an,rate
R2164 T7441 T7439 dobj rate,ensure
R2165 T7442 T7441 amod overall,rate
R2166 T7443 T7444 amod false,positive
R2167 T7444 T7441 amod positive,rate
R2168 T7445 T7441 prep of,rate
R2169 T7446 T7447 nummod 5,%
R2170 T7447 T7445 pobj %,of
R2171 T7448 T7424 punct ", ",suggested
R2172 T7449 T7450 dep which,means
R2173 T7450 T7424 advcl means,suggested
R2174 T7451 T7452 mark that,prevent
R2175 T7452 T7450 ccomp prevent,means
R2176 T7453 T7452 csubj using,prevent
R2177 T7454 T7455 det a,value
R2178 T7455 T7453 dobj value,using
R2179 T7456 T7455 amod lower,value
R2180 T7457 T7455 compound threshold,value
R2181 T7458 T7452 aux will,prevent
R2182 T7459 T7460 amod false,negative
R2183 T7460 T7461 amod negative,QTL
R2184 T7461 T7452 dobj QTL,prevent
R2185 T7462 T7452 prep at,prevent
R2186 T7463 T7464 det the,expense
R2187 T7464 T7462 pobj expense,at
R2188 T7465 T7464 prep of,expense
R2189 T7466 T7465 pcomp increasing,of
R2190 T7467 T7468 amod false,positive
R2191 T7468 T7469 amod positive,QTL
R2192 T7469 T7466 dobj QTL,increasing
R2193 T7470 T7424 punct .,suggested
R2194 T7472 T7473 advcl Being,examined
R2195 T7474 T7472 acomp aware,Being
R2196 T7475 T7474 prep of,aware
R2197 T7476 T7475 pobj this,of
R2198 T7477 T7473 punct ", ",examined
R2199 T7478 T7473 nsubj we,examined
R2200 T7479 T7480 det these,regions
R2201 T7480 T7473 dobj regions,examined
R2202 T7481 T7480 amod genomic,regions
R2203 T7482 T7483 aux to,search
R2204 T7483 T7473 advcl search,examined
R2205 T7484 T7485 mark whether,linked
R2206 T7485 T7483 ccomp linked,search
R2207 T7486 T7485 nsubjpass they,linked
R2208 T7487 T7486 punct ", ",they
R2209 T7488 T7486 cc or,they
R2210 T7489 T7490 poss their,regions
R2211 T7490 T7486 conj regions,they
R2212 T7491 T7490 amod syntenic,regions
R2213 T7492 T7490 amod genomic,regions
R2214 T7493 T7490 prep on,regions
R2215 T7494 T7495 det the,genome
R2216 T7495 T7493 pobj genome,on
R2217 T7496 T7495 amod human,genome
R2218 T7497 T7485 punct ", ",linked
R2219 T7498 T7485 aux have,linked
R2220 T7499 T7485 auxpass been,linked
R2221 T7500 T7485 advmod previously,linked
R2222 T7501 T7485 prep to,linked
R2223 T7502 T7501 pobj arthritis,to
R2224 T7503 T7473 punct .,examined
R2225 T7505 T7506 nummod Four,QTL
R2226 T7506 T7510 nsubj QTL,overlapped
R2227 T7507 T7508 amod small,effect
R2228 T7508 T7506 compound effect,QTL
R2229 T7509 T7508 punct -,effect
R2230 T7511 T7510 prep with,overlapped
R2231 T7512 T7513 compound arthritis,QTL
R2232 T7513 T7511 pobj QTL,with
R2233 T7514 T7510 prep on,overlapped
R2234 T7515 T7516 det the,genome
R2235 T7516 T7514 pobj genome,on
R2236 T7517 T7516 compound mouse,genome
R2237 T7518 T7516 acl identified,genome
R2238 T7519 T7518 advmod previously,identified
R2239 T7520 T7510 punct .,overlapped
R2240 T7522 T7523 nmod Locus,1
R2241 T7523 T7524 nsubj 1,overlap
R2242 T7525 T7523 cc and,1
R2243 T7526 T7523 conj 2,1
R2244 T7527 T7524 prep with,overlap
R2245 T7528 T7527 pobj Cia13,with
R2246 T7529 T7528 cc and,Cia13
R2247 T7530 T7528 conj Cia14,Cia13
R2248 T7531 T7528 punct ", ",Cia13
R2249 T7532 T7533 dep which,control
R2250 T7533 T7528 relcl control,Cia13
R2251 T7534 T7533 dobj severity,control
R2252 T7535 T7534 prep of,severity
R2253 T7536 T7535 pobj CIA,of
R2254 T7537 T7533 prep in,control
R2255 T7538 T7539 punct (,DBA
R2256 T7539 T7540 nmod DBA,progeny
R2257 T7540 T7537 pobj progeny,in
R2258 T7541 T7539 punct /,DBA
R2259 T7542 T7539 nummod 1,DBA
R2260 T7543 T7539 punct ×,DBA
R2261 T7544 T7545 compound BALB,C
R2262 T7545 T7539 appos C,DBA
R2263 T7546 T7545 punct /,C
R2264 T7547 T7539 punct ),DBA
R2265 T7548 T7540 compound F2,progeny
R2266 T7549 T7550 punct [,27
R2267 T7550 T7524 parataxis 27,overlap
R2268 T7551 T7550 punct ],27
R2269 T7552 T7524 punct .,overlap
R2270 T7554 T7555 nsubj Locus,overlaps
R2271 T7556 T7554 nummod 5,Locus
R2272 T7557 T7554 acl located,Locus
R2273 T7558 T7557 prep on,located
R2274 T7559 T7558 pobj chromosome,on
R2275 T7560 T7559 nummod 10,chromosome
R2276 T7561 T7555 prep with,overlaps
R2277 T7562 T7561 pobj Cia8,with
R2278 T7563 T7562 punct ", ",Cia8
R2279 T7564 T7565 dep which,identified
R2280 T7565 T7562 relcl identified,Cia8
R2281 T7566 T7565 auxpass was,identified
R2282 T7567 T7565 prep in,identified
R2283 T7568 T7569 punct (,DBA
R2284 T7569 T7570 nmod DBA,progeny
R2285 T7570 T7567 pobj progeny,in
R2286 T7571 T7569 punct /,DBA
R2287 T7572 T7569 nummod 1,DBA
R2288 T7573 T7569 punct ×,DBA
R2289 T7574 T7569 appos B10.Q,DBA
R2290 T7575 T7570 punct ),progeny
R2291 T7576 T7570 compound F2,progeny
R2292 T7577 T7578 punct [,28
R2293 T7578 T7555 parataxis 28,overlaps
R2294 T7579 T7578 punct ],28
R2295 T7580 T7555 punct .,overlaps
R2296 T7582 T7583 nsubj Locus,overlaps
R2297 T7584 T7582 nummod 6,Locus
R2298 T7585 T7583 prep with,overlaps
R2299 T7586 T7585 pobj Pgia7,with
R2300 T7587 T7586 punct ", ",Pgia7
R2301 T7588 T7589 dep which,controls
R2302 T7589 T7586 relcl controls,Pgia7
R2303 T7590 T7589 dobj susceptibility,controls
R2304 T7591 T7590 prep to,susceptibility
R2305 T7592 T7593 npadvmod proteoglycan,induced
R2306 T7593 T7595 amod induced,arthritis
R2307 T7594 T7593 punct -,induced
R2308 T7595 T7591 pobj arthritis,to
R2309 T7596 T7595 punct (,arthritis
R2310 T7597 T7595 appos PGIA,arthritis
R2311 T7598 T7589 punct ),controls
R2312 T7599 T7589 cc and,controls
R2313 T7600 T7601 auxpass was,identified
R2314 T7601 T7589 conj identified,controls
R2315 T7602 T7601 prep in,identified
R2316 T7603 T7604 punct (,C
R2317 T7604 T7607 nmod C,progeny
R2318 T7605 T7604 nmod BALB,C
R2319 T7606 T7604 punct /,C
R2320 T7607 T7602 pobj progeny,in
R2321 T7608 T7604 punct ×,C
R2322 T7609 T7604 appos DBA,C
R2323 T7610 T7609 punct /,DBA
R2324 T7611 T7609 nummod 2,DBA
R2325 T7612 T7604 punct ),C
R2326 T7613 T7607 compound F2,progeny
R2327 T7614 T7615 punct [,29
R2328 T7615 T7583 parataxis 29,overlaps
R2329 T7616 T7615 punct ],29
R2330 T7617 T7583 punct .,overlaps
R2331 T7619 T7620 det The,regions
R2332 T7620 T7623 nsubjpass regions,reported
R2333 T7621 T7620 amod syntenic,regions
R2334 T7622 T7620 amod genomic,regions
R2335 T7624 T7620 prep of,regions
R2336 T7625 T7626 nummod five,QTL
R2337 T7626 T7624 pobj QTL,of
R2338 T7627 T7628 amod small,effect
R2339 T7628 T7626 compound effect,QTL
R2340 T7629 T7628 punct -,effect
R2341 T7630 T7626 prep on,QTL
R2342 T7631 T7632 det the,genome
R2343 T7632 T7630 pobj genome,on
R2344 T7633 T7632 amod human,genome
R2345 T7634 T7623 aux have,reported
R2346 T7635 T7623 auxpass been,reported
R2347 T7636 T7637 aux to,linked
R2348 T7637 T7623 xcomp linked,reported
R2349 T7638 T7637 auxpass be,linked
R2350 T7639 T7637 prep to,linked
R2351 T7640 T7639 pobj RA,to
R2352 T7641 T7623 punct .,reported
R2353 T7643 T7644 nsubj These,are
R2354 T7645 T7646 amod genomic,regions
R2355 T7646 T7644 attr regions,are
R2356 T7647 T7646 appos 22q11,regions
R2357 T7648 T7647 cc and,22q11
R2358 T7649 T7650 compound 12p13,q24
R2359 T7650 T7647 conj q24,22q11
R2360 T7651 T7650 punct -,q24
R2361 T7652 T7646 prep on,regions
R2362 T7653 T7654 nmod chromosome,22
R2363 T7654 T7652 pobj 22,on
R2364 T7655 T7654 cc and,22
R2365 T7656 T7654 conj 12,22
R2366 T7657 T7658 punct (,counterparts
R2367 T7658 T7646 parataxis counterparts,regions
R2368 T7659 T7658 det the,counterparts
R2369 T7660 T7658 prep of,counterparts
R2370 T7661 T7660 pobj locus,of
R2371 T7662 T7661 nummod 2,locus
R2372 T7663 T7658 punct ),counterparts
R2373 T7664 T7646 punct ", ",regions
R2374 T7665 T7666 compound 12p13,pter
R2375 T7666 T7646 conj pter,regions
R2376 T7667 T7666 punct -,pter
R2377 T7668 T7666 prep on,pter
R2378 T7669 T7668 pobj chromosome,on
R2379 T7670 T7669 nummod 12,chromosome
R2380 T7671 T7672 punct (,counterpart
R2381 T7672 T7666 parataxis counterpart,pter
R2382 T7673 T7672 det the,counterpart
R2383 T7674 T7672 prep of,counterpart
R2384 T7675 T7674 pobj locus,of
R2385 T7676 T7675 nummod 3,locus
R2386 T7677 T7672 punct ),counterpart
R2387 T7678 T7666 punct ", ",pter
R2388 T7679 T7680 compound 21q22,qter
R2389 T7680 T7666 conj qter,pter
R2390 T7681 T7680 punct -,qter
R2391 T7682 T7680 cc and,qter
R2392 T7683 T7680 conj 10q22,qter
R2393 T7684 T7683 punct -,10q22
R2394 T7685 T7683 nummod 23,10q22
R2395 T7686 T7680 prep on,qter
R2396 T7687 T7688 nmod chromosome,21
R2397 T7688 T7686 pobj 21,on
R2398 T7689 T7688 cc and,21
R2399 T7690 T7688 conj 10,21
R2400 T7691 T7692 punct (,counterparts
R2401 T7692 T7680 parataxis counterparts,qter
R2402 T7693 T7692 det the,counterparts
R2403 T7694 T7692 prep of,counterparts
R2404 T7695 T7694 pobj locus,of
R2405 T7696 T7695 nummod 5,locus
R2406 T7697 T7692 punct ),counterparts
R2407 T7698 T7680 punct ", ",qter
R2408 T7699 T7680 conj 17q21,qter
R2409 T7700 T7699 punct -,17q21
R2410 T7701 T7699 nummod 25,17q21
R2411 T7702 T7699 prep on,17q21
R2412 T7703 T7702 pobj chromosome,on
R2413 T7704 T7703 nummod 17,chromosome
R2414 T7705 T7706 punct (,counterpart
R2415 T7706 T7699 parataxis counterpart,17q21
R2416 T7707 T7706 det the,counterpart
R2417 T7708 T7706 prep of,counterpart
R2418 T7709 T7708 pobj locus,of
R2419 T7710 T7709 nummod 6,locus
R2420 T7711 T7706 punct ),counterpart
R2421 T7712 T7699 cc and,17q21
R2422 T7713 T7714 compound 3q29,qter
R2423 T7714 T7699 conj qter,17q21
R2424 T7715 T7714 punct -,qter
R2425 T7716 T7714 prep on,qter
R2426 T7717 T7716 pobj chromosome,on
R2427 T7718 T7717 nummod 3,chromosome
R2428 T7719 T7720 punct (,counterpart
R2429 T7720 T7714 parataxis counterpart,qter
R2430 T7721 T7720 det the,counterpart
R2431 T7722 T7720 prep of,counterpart
R2432 T7723 T7722 pobj locus,of
R2433 T7724 T7723 nummod 7,locus
R2434 T7725 T7720 punct ),counterpart
R2435 T7726 T7727 punct [,4
R2436 T7727 T7644 parataxis 4,are
R2437 T7728 T7727 nummod 2,4
R2438 T7729 T7727 punct ",",4
R2439 T7730 T7727 punct ],4
R2440 T7731 T7644 punct .,are