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PMC:1892049 / 17804-19164 JSONTXT

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craft-ca-core-ex-dev

Below, discontinuous spans are shown in the chain model. You can change it to the bag model.

Id Subject Object Predicate Lexical cue
T6329 54-59 NCBITaxon:10088 denotes mouse
T6330 60-69 SO_EXT:sequence_alteration_entity_or_process denotes mutations
T6331 87-92 NCBITaxon:9606 denotes human
T6332 133-137 GO_PATO_EXT:aging_or_agedness denotes aged
T6333 138-143 PR_EXT:000009158 denotes Itpr1
T6334 143-145 SO_EXT:wild_type_entity_or_quality denotes wt
T6335 150-157 NCBITaxon:33208 denotes animals
T6336 192-196 NCBITaxon:10088 denotes mice
T6337 283-287 NCBITaxon:10088 denotes mice
T6338 382-388 SO_EXT:0001026 denotes genome
T6339 394-397 SO_EXT:0000694 denotes SNP
T6340 449-456 SO_EXT:0001026 denotes genomic
T6341 457-466 SO_EXT:sequence_alteration_entity_or_process denotes mutations
T6342 578-586 SO_EXT:sequence_deletion_entity_or_process denotes deletion
T6343 590-595 PR_EXT:000009158 denotes ITPR1
T6344 619-627 SO_EXT:biological_sequence denotes sequence
T6345 640-645 PR_EXT:000009158 denotes ITPR1
T6346 743-751 SO_EXT:sequence_alteration_entity_or_process denotes mutation
T6347 788-798 SO_EXT:sequence_alteration_entity_or_process denotes mutational
T6348 909-914 PR_EXT:000009158 denotes ITPR1
T6349 915-923 SO_EXT:sequence_alteration_entity_or_process denotes mutation
T6350 963-967 SO_EXT:0000704 denotes gene
T6351 1023-1032 GO:0030849 denotes autosomal
T6352 1159-1164 PR_EXT:000009158 denotes ITPR1
T6353 1170-1174 SO_EXT:0000704 denotes gene
T6354 1267-1280 GO:0005622 denotes intracellular
T6355 1267-1280 _FRAGMENT denotes intracellular
T6356 1286-1295 GO:0035556 denotes signaling
T6357 1272-1280 CL_GO_EXT:cell denotes cellular
T6358 1281-1285 CHEBI:29108 denotes Ca2+
T6359 1281-1295 GO:0019722 denotes Ca2+ signaling
T6360 1299-1313 CL:0000121 denotes Purkinje cells
T6361 1308-1313 CL_GO_EXT:cell denotes cells
T6362 1337-1352 UBERON:0014643 denotes spinocerebellar
R407 T6356 T6355 _lexicallyChainedTo signaling,intracellular

craft-ca-core-dev

Below, discontinuous spans are shown in the chain model. You can change it to the bag model.

Id Subject Object Predicate Lexical cue
T5992 54-59 NCBITaxon:10088 denotes mouse
T5993 87-92 NCBITaxon:9606 denotes human
T5994 138-143 PR:000009158 denotes Itpr1
T5995 150-157 NCBITaxon:33208 denotes animals
T5996 192-196 NCBITaxon:10088 denotes mice
T5997 283-287 NCBITaxon:10088 denotes mice
T5998 382-388 SO:0001026 denotes genome
T5999 394-397 SO:0000694 denotes SNP
T6000 449-456 SO:0001026 denotes genomic
T6001 590-595 PR:000009158 denotes ITPR1
T6002 640-645 PR:000009158 denotes ITPR1
T6003 909-914 PR:000009158 denotes ITPR1
T6004 963-967 SO:0000704 denotes gene
T6005 1023-1032 GO:0030849 denotes autosomal
T6006 1159-1164 PR:000009158 denotes ITPR1
T6007 1170-1174 SO:0000704 denotes gene
T6008 1267-1280 GO:0005622 denotes intracellular
T6009 1267-1280 _FRAGMENT denotes intracellular
T6010 1286-1295 GO:0035556 denotes signaling
T6011 1281-1285 CHEBI:29108 denotes Ca2+
T6012 1281-1295 GO:0019722 denotes Ca2+ signaling
T6013 1299-1313 CL:0000121 denotes Purkinje cells
T6014 1337-1352 UBERON:0014643 denotes spinocerebellar
R400 T6010 T6009 _lexicallyChainedTo signaling,intracellular

craft-sa-dev

Id Subject Object Predicate Lexical cue
T8381 0-2 PRP denotes We
T8382 3-7 VBP denotes show
T8383 8-12 RB denotes here
T8384 13-16 DT denotes the
T8385 17-24 NN denotes utility
T8386 25-27 IN denotes of
T8387 28-41 VBG denotes investigating
T8388 42-53 JJ denotes spontaneous
T8389 60-69 NNS denotes mutations
T8390 54-59 NN denotes mouse
T8391 70-72 IN denotes in
T8392 73-86 VBG denotes understanding
T8393 87-92 JJ denotes human
T8394 93-100 NN denotes disease
T8395 100-101 . denotes .
T8396 101-348 sentence denotes Currently, the small number of aged Itpr1wt/Δ18 animals precludes us from examining these mice for subtle signs and symptoms similar to those seen in SCA15 patients; however, these mice are clearly of interest to us as a potential model of SCA15.
T8397 102-111 RB denotes Currently
T8398 158-167 VBZ denotes precludes
T8399 111-113 , denotes ,
T8400 113-116 DT denotes the
T8401 123-129 NN denotes number
T8402 117-122 JJ denotes small
T8403 130-132 IN denotes of
T8404 133-137 VBN denotes aged
T8405 150-157 NNS denotes animals
T8406 138-145 NN denotes Itpr1wt
T8407 146-149 NN denotes Δ18
T8408 145-146 HYPH denotes /
T8409 288-291 VBP denotes are
T8410 168-170 PRP denotes us
T8411 171-175 IN denotes from
T8412 176-185 VBG denotes examining
T8413 186-191 DT denotes these
T8414 192-196 NNS denotes mice
T8415 197-200 IN denotes for
T8416 201-207 JJ denotes subtle
T8417 208-213 NNS denotes signs
T8418 214-217 CC denotes and
T8419 218-226 NNS denotes symptoms
T8420 227-234 JJ denotes similar
T8421 235-237 IN denotes to
T8422 238-243 DT denotes those
T8423 244-248 VBN denotes seen
T8424 249-251 IN denotes in
T8425 252-257 NN denotes SCA15
T8426 258-266 NNS denotes patients
T8427 266-267 : denotes ;
T8428 268-275 RB denotes however
T8429 275-277 , denotes ,
T8430 277-282 DT denotes these
T8431 283-287 NNS denotes mice
T8432 292-299 RB denotes clearly
T8433 300-302 IN denotes of
T8434 303-311 NN denotes interest
T8435 312-314 IN denotes to
T8436 315-317 PRP denotes us
T8437 318-320 IN denotes as
T8438 321-322 DT denotes a
T8439 333-338 NN denotes model
T8440 323-332 JJ denotes potential
T8441 339-341 IN denotes of
T8442 342-347 NN denotes SCA15
T8443 347-348 . denotes .
T8444 348-493 sentence denotes These data also demonstrate that genome-wide SNP assay can facilitate rapid detection of structural genomic mutations that may underlie disease.
T8445 349-354 DT denotes These
T8446 355-359 NNS denotes data
T8447 365-376 VBP denotes demonstrate
T8448 360-364 RB denotes also
T8449 377-381 IN denotes that
T8450 408-418 VB denotes facilitate
T8451 382-388 NN denotes genome
T8452 389-393 JJ denotes wide
T8453 388-389 HYPH denotes -
T8454 398-403 NN denotes assay
T8455 394-397 NN denotes SNP
T8456 404-407 MD denotes can
T8457 419-424 JJ denotes rapid
T8458 425-434 NN denotes detection
T8459 435-437 IN denotes of
T8460 438-448 JJ denotes structural
T8461 457-466 NNS denotes mutations
T8462 449-456 JJ denotes genomic
T8463 467-471 WDT denotes that
T8464 476-484 VB denotes underlie
T8465 472-475 MD denotes may
T8466 485-492 NN denotes disease
T8467 492-493 . denotes .
T8468 493-609 sentence denotes The data provided by these approaches provide compelling evidence that heterozygous deletion of ITPR1 causes SCA15.
T8469 494-497 DT denotes The
T8470 498-502 NNS denotes data
T8471 532-539 VBP denotes provide
T8472 503-511 VBN denotes provided
T8473 512-514 IN denotes by
T8474 515-520 DT denotes these
T8475 521-531 NNS denotes approaches
T8476 540-550 JJ denotes compelling
T8477 551-559 NN denotes evidence
T8478 560-564 IN denotes that
T8479 596-602 VBZ denotes causes
T8480 565-577 JJ denotes heterozygous
T8481 578-586 NN denotes deletion
T8482 587-589 IN denotes of
T8483 590-595 NN denotes ITPR1
T8484 603-608 NN denotes SCA15
T8485 608-609 . denotes .
T8486 609-1001 sentence denotes Clearly, sequence analysis of ITPR1 in potential SCA15 cases may provide additional insight into the disease, particularly if a stop mutation were to be identified; however, the mutational mechanism noted here means that standard sequencing approaches alone are insufficient to confidently rule out ITPR1 mutation as a cause of disease: a comprehensive gene dosage approach is also required.
T8487 610-617 RB denotes Clearly
T8488 675-682 VB denotes provide
T8489 617-619 , denotes ,
T8490 619-627 NN denotes sequence
T8491 628-636 NN denotes analysis
T8492 637-639 IN denotes of
T8493 640-645 NN denotes ITPR1
T8494 646-648 IN denotes in
T8495 649-658 JJ denotes potential
T8496 665-670 NNS denotes cases
T8497 659-664 NN denotes SCA15
T8498 671-674 MD denotes may
T8499 820-825 VBZ denotes means
T8500 683-693 JJ denotes additional
T8501 694-701 NN denotes insight
T8502 702-706 IN denotes into
T8503 707-710 DT denotes the
T8504 711-718 NN denotes disease
T8505 718-720 , denotes ,
T8506 720-732 RB denotes particularly
T8507 752-756 VBD denotes were
T8508 733-735 IN denotes if
T8509 736-737 DT denotes a
T8510 743-751 NN denotes mutation
T8511 738-742 NN denotes stop
T8512 757-759 TO denotes to
T8513 763-773 VBN denotes identified
T8514 760-762 VB denotes be
T8515 773-774 : denotes ;
T8516 775-782 RB denotes however
T8517 782-784 , denotes ,
T8518 784-787 DT denotes the
T8519 799-808 NN denotes mechanism
T8520 788-798 JJ denotes mutational
T8521 809-814 VBN denotes noted
T8522 815-819 RB denotes here
T8523 826-830 IN denotes that
T8524 992-1000 VBN denotes required
T8525 831-839 JJ denotes standard
T8526 851-861 NNS denotes approaches
T8527 840-850 NN denotes sequencing
T8528 868-871 VBP denotes are
T8529 862-867 RB denotes alone
T8530 872-884 JJ denotes insufficient
T8531 885-887 TO denotes to
T8532 900-904 VB denotes rule
T8533 888-899 RB denotes confidently
T8534 905-908 RP denotes out
T8535 909-914 NN denotes ITPR1
T8536 915-923 NN denotes mutation
T8537 924-926 IN denotes as
T8538 927-928 DT denotes a
T8539 929-934 NN denotes cause
T8540 935-937 IN denotes of
T8541 938-945 NN denotes disease
T8542 945-947 : denotes :
T8543 947-948 DT denotes a
T8544 975-983 NN denotes approach
T8545 949-962 JJ denotes comprehensive
T8546 963-967 NN denotes gene
T8547 968-974 NN denotes dosage
T8548 984-986 VBZ denotes is
T8549 987-991 RB denotes also
T8550 1000-1001 . denotes .
T8551 1001-1221 sentence denotes Given that SCA16 and autosomal dominant congenital nonprogressive ataxia have both recently been mapped to regions overlapping with the SCA15 locus [10,11], ITPR1 is a gene of importance for screening in these families.
T8552 1002-1007 VBN denotes Given
T8553 1165-1167 VBZ denotes is
T8554 1008-1012 IN denotes that
T8555 1099-1105 VBN denotes mapped
T8556 1013-1018 NN denotes SCA16
T8557 1019-1022 CC denotes and
T8558 1023-1032 JJ denotes autosomal
T8559 1068-1074 NN denotes ataxia
T8560 1033-1041 JJ denotes dominant
T8561 1042-1052 JJ denotes congenital
T8562 1053-1067 JJ denotes nonprogressive
T8563 1075-1079 VBP denotes have
T8564 1080-1084 DT denotes both
T8565 1085-1093 RB denotes recently
T8566 1094-1098 VBN denotes been
T8567 1106-1108 IN denotes to
T8568 1109-1116 NNS denotes regions
T8569 1117-1128 VBG denotes overlapping
T8570 1129-1133 IN denotes with
T8571 1134-1137 DT denotes the
T8572 1144-1149 NN denotes locus
T8573 1138-1143 NN denotes SCA15
T8574 1150-1151 -LRB- denotes [
T8575 1154-1156 CD denotes 11
T8576 1151-1153 CD denotes 10
T8577 1153-1154 , denotes ,
T8578 1156-1157 -RRB- denotes ]
T8579 1157-1159 , denotes ,
T8580 1159-1164 NN denotes ITPR1
T8581 1168-1169 DT denotes a
T8582 1170-1174 NN denotes gene
T8583 1175-1177 IN denotes of
T8584 1178-1188 NN denotes importance
T8585 1189-1192 IN denotes for
T8586 1193-1202 NN denotes screening
T8587 1203-1205 IN denotes in
T8588 1206-1211 DT denotes these
T8589 1212-1220 NNS denotes families
T8590 1220-1221 . denotes .
T8591 1221-1360 sentence denotes These data add weight to a role for aberrant intracellular Ca2+ signaling in Purkinje cells in the pathogenesis of spinocerebellar ataxia.
T8592 1222-1227 DT denotes These
T8593 1228-1232 NNS denotes data
T8594 1233-1236 VBP denotes add
T8595 1237-1243 NN denotes weight
T8596 1244-1246 IN denotes to
T8597 1247-1248 DT denotes a
T8598 1249-1253 NN denotes role
T8599 1254-1257 IN denotes for
T8600 1258-1266 JJ denotes aberrant
T8601 1286-1295 NN denotes signaling
T8602 1267-1280 JJ denotes intracellular
T8603 1281-1285 NN denotes Ca2+
T8604 1296-1298 IN denotes in
T8605 1299-1307 NNP denotes Purkinje
T8606 1308-1313 NNS denotes cells
T8607 1314-1316 IN denotes in
T8608 1317-1320 DT denotes the
T8609 1321-1333 NN denotes pathogenesis
T8610 1334-1336 IN denotes of
T8611 1337-1352 JJ denotes spinocerebellar
T8612 1353-1359 NN denotes ataxia
T8613 1359-1360 . denotes .
R2230 T8383 T8382 advmod here,show
R2232 T8384 T8385 det the,utility
R2233 T8385 T8382 dobj utility,show
R2236 T8386 T8385 prep of,utility
R2238 T8387 T8386 pcomp investigating,of
R2239 T8388 T8389 amod spontaneous,mutations
R2240 T8389 T8387 dobj mutations,investigating
R2242 T8390 T8389 compound mouse,mutations
R2243 T8391 T8387 prep in,investigating
R2244 T8392 T8391 pcomp understanding,in
R2246 T8393 T8394 amod human,disease
R2247 T8394 T8392 dobj disease,understanding
R2249 T8395 T8382 punct .,show
R2251 T8397 T8398 advmod Currently,precludes
R2252 T8398 T8409 ccomp precludes,are
R2253 T8399 T8398 punct ", ",precludes
R2255 T8400 T8401 det the,number
R2256 T8401 T8398 nsubj number,precludes
R2258 T8402 T8401 amod small,number
R2259 T8403 T8401 prep of,number
R2260 T8404 T8405 amod aged,animals
R2262 T8405 T8403 pobj animals,of
R2263 T8406 T8407 compound Itpr1wt,Δ18
R2264 T8407 T8405 compound Δ18,animals
R2266 T8408 T8407 punct /,Δ18
R2267 T8410 T8398 dobj us,precludes
R2269 T8411 T8398 prep from,precludes
R2270 T8412 T8411 pcomp examining,from
R2271 T8413 T8414 det these,mice
R2272 T8414 T8412 dobj mice,examining
R2273 T8415 T8412 prep for,examining
R2275 T8416 T8417 amod subtle,signs
R2276 T8417 T8415 pobj signs,for
R2277 T8418 T8417 cc and,signs
R2279 T8419 T8417 conj symptoms,signs
R2280 T8420 T8417 amod similar,signs
R2281 T8421 T8420 prep to,similar
R2283 T8422 T8421 pobj those,to
R2284 T8423 T8422 acl seen,those
R2286 T8424 T8423 prep in,seen
R2287 T8425 T8426 compound SCA15,patients
R2288 T8426 T8424 pobj patients,in
R2290 T8427 T8409 punct ;,are
R2291 T8428 T8409 advmod however,are
R2292 T8429 T8409 punct ", ",are
R2294 T8430 T8431 det these,mice
R2295 T8431 T8409 nsubj mice,are
R2296 T8432 T8409 advmod clearly,are
R2297 T8433 T8409 prep of,are
R2299 T8434 T8433 pobj interest,of
R2300 T8435 T8434 prep to,interest
R2302 T8436 T8435 pobj us,to
R2303 T8437 T8409 prep as,are
R2304 T8438 T8439 det a,model
R2306 T8439 T8437 pobj model,as
R2307 T8440 T8439 amod potential,model
R2308 T8441 T8439 prep of,model
R2310 T8442 T8441 pobj SCA15,of
R2311 T8443 T8409 punct .,are
R2313 T8445 T8446 det These,data
R2314 T8446 T8447 nsubj data,demonstrate
R2316 T8448 T8447 advmod also,demonstrate
R2318 T8449 T8450 mark that,facilitate
R2319 T8450 T8447 ccomp facilitate,demonstrate
R2320 T8451 T8452 npadvmod genome,wide
R2321 T8452 T8454 amod wide,assay
R2322 T8453 T8452 punct -,wide
R2323 T8454 T8450 nsubj assay,facilitate
R2325 T8455 T8454 compound SNP,assay
R2326 T8456 T8450 aux can,facilitate
R2327 T8457 T8458 amod rapid,detection
R2328 T8458 T8450 dobj detection,facilitate
R2330 T8459 T8458 prep of,detection
R2331 T8460 T8461 amod structural,mutations
R2332 T8461 T8459 pobj mutations,of
R2334 T8462 T8461 amod genomic,mutations
R2335 T8463 T8464 dep that,underlie
R2337 T8464 T8461 relcl underlie,mutations
R2338 T8465 T8464 aux may,underlie
R2339 T8466 T8464 dobj disease,underlie
R2341 T8467 T8447 punct .,demonstrate
R2343 T8469 T8470 det The,data
R2344 T8470 T8471 nsubj data,provide
R2346 T8472 T8470 acl provided,data
R2349 T8473 T8472 agent by,provided
R2350 T8474 T8475 det these,approaches
R2352 T8475 T8473 pobj approaches,by
R2353 T8476 T8477 amod compelling,evidence
R2355 T8477 T8471 dobj evidence,provide
R2356 T8478 T8479 mark that,causes
R2357 T8479 T8477 acl causes,evidence
R2359 T8480 T8481 amod heterozygous,deletion
R2362 T8481 T8479 nsubj deletion,causes
R2364 T8482 T8481 prep of,deletion
R2365 T8483 T8482 pobj ITPR1,of
R2366 T8484 T8479 dobj SCA15,causes
R2368 T8485 T8471 punct .,provide
R2370 T8487 T8488 advmod Clearly,provide
R2371 T8488 T8499 ccomp provide,means
R2375 T8489 T8488 punct ", ",provide
R2377 T8490 T8491 compound sequence,analysis
R2378 T8491 T8488 nsubj analysis,provide
R2380 T8492 T8491 prep of,analysis
R2381 T8493 T8492 pobj ITPR1,of
R2382 T8494 T8493 prep in,ITPR1
R2384 T8495 T8496 amod potential,cases
R2385 T8496 T8494 pobj cases,in
R2387 T8497 T8496 compound SCA15,cases
R2388 T8498 T8488 aux may,provide
R2390 T8500 T8501 amod additional,insight
R2391 T8501 T8488 dobj insight,provide
R2393 T8502 T8501 prep into,insight
R2394 T8503 T8504 det the,disease
R2395 T8504 T8502 pobj disease,into
R2397 T8505 T8488 punct ", ",provide
R2398 T8506 T8507 advmod particularly,were
R2399 T8507 T8488 advcl were,provide
R2401 T8508 T8507 mark if,were
R2402 T8509 T8510 det a,mutation
R2404 T8510 T8507 nsubj mutation,were
R2405 T8511 T8510 compound stop,mutation
R2406 T8512 T8513 aux to,identified
R2408 T8513 T8507 xcomp identified,were
R2409 T8514 T8513 auxpass be,identified
R2410 T8515 T8499 punct ;,means
R2412 T8516 T8499 advmod however,means
R2413 T8517 T8499 punct ", ",means
R2415 T8518 T8519 det the,mechanism
R2416 T8519 T8499 nsubj mechanism,means
R2417 T8520 T8519 amod mutational,mechanism
R2419 T8521 T8519 acl noted,mechanism
R2420 T8522 T8521 advmod here,noted
R2422 T8523 T8524 mark that,required
R2423 T8524 T8499 ccomp required,means
R2424 T8525 T8526 amod standard,approaches
R2425 T8526 T8528 nsubj approaches,are
R2426 T8527 T8526 compound sequencing,approaches
R2427 T8528 T8524 ccomp are,required
R2429 T8529 T8526 advmod alone,approaches
R2430 T8530 T8528 acomp insufficient,are
R2432 T8531 T8532 aux to,rule
R2433 T8532 T8530 xcomp rule,insufficient
R2434 T8533 T8532 advmod confidently,rule
R2436 T8534 T8532 prt out,rule
R2437 T8535 T8536 compound ITPR1,mutation
R2438 T8536 T8532 dobj mutation,rule
R2440 T8537 T8532 prep as,rule
R2441 T8538 T8539 det a,cause
R2443 T8539 T8537 pobj cause,as
R2444 T8540 T8539 prep of,cause
R2446 T8541 T8540 pobj disease,of
R2447 T8542 T8524 punct : ,required
R2449 T8543 T8544 det a,approach
R2450 T8544 T8524 nsubjpass approach,required
R2451 T8545 T8544 amod comprehensive,approach
R2452 T8546 T8547 compound gene,dosage
R2454 T8547 T8544 compound dosage,approach
R2455 T8548 T8524 auxpass is,required
R2456 T8549 T8524 advmod also,required
R2457 T8550 T8499 punct .,means
R2459 T8552 T8553 prep Given,is
R2461 T8554 T8555 mark that,mapped
R2464 T8555 T8552 pcomp mapped,Given
R2465 T8556 T8555 nsubjpass SCA16,mapped
R2466 T8557 T8556 cc and,SCA16
R2468 T8558 T8559 amod autosomal,ataxia
R2469 T8559 T8556 conj ataxia,SCA16
R2471 T8560 T8559 amod dominant,ataxia
R2472 T8561 T8559 amod congenital,ataxia
R2474 T8562 T8559 amod nonprogressive,ataxia
R2475 T8563 T8555 aux have,mapped
R2476 T8564 T8555 dep both,mapped
R2477 T8565 T8555 advmod recently,mapped
R2478 T8566 T8555 auxpass been,mapped
R2480 T8567 T8555 prep to,mapped
R2481 T8568 T8567 pobj regions,to
R2482 T8569 T8568 acl overlapping,regions
R2484 T8570 T8569 prep with,overlapping
R2485 T8571 T8572 det the,locus
R2486 T8572 T8570 pobj locus,with
R2488 T8573 T8572 compound SCA15,locus
R2489 T8574 T8575 punct [,11
R2491 T8575 T8555 parataxis 11,mapped
R2492 T8576 T8575 nummod 10,11
R2493 T8577 T8575 punct ",",11
R2495 T8578 T8575 punct ],11
R2496 T8579 T8553 punct ", ",is
R2497 T8580 T8553 nsubj ITPR1,is
R2499 T8581 T8582 det a,gene
R2500 T8582 T8553 attr gene,is
R2502 T8583 T8582 prep of,gene
R2503 T8584 T8583 pobj importance,of
R2504 T8585 T8584 prep for,importance
R2505 T8586 T8585 pobj screening,for
R2507 T8587 T8553 prep in,is
R2508 T8588 T8589 det these,families
R2509 T8589 T8587 pobj families,in
R2511 T8590 T8553 punct .,is
R2513 T8592 T8593 det These,data
R2514 T8593 T8594 nsubj data,add
R2515 T8381 T8382 nsubj We,show
R2516 T8595 T8594 dobj weight,add
R2517 T8596 T8594 prep to,add
R2518 T8597 T8598 det a,role
R2519 T8598 T8596 pobj role,to
R2520 T8599 T8598 prep for,role
R2521 T8600 T8601 amod aberrant,signaling
R2522 T8601 T8599 pobj signaling,for
R2523 T8602 T8601 amod intracellular,signaling
R2524 T8603 T8601 compound Ca2+,signaling
R2525 T8604 T8601 prep in,signaling
R2526 T8605 T8606 compound Purkinje,cells
R2527 T8606 T8604 pobj cells,in
R2528 T8607 T8598 prep in,role
R2529 T8608 T8609 det the,pathogenesis
R2530 T8609 T8607 pobj pathogenesis,in
R2531 T8610 T8609 prep of,pathogenesis
R2532 T8611 T8612 amod spinocerebellar,ataxia
R2533 T8612 T8610 pobj ataxia,of
R2534 T8613 T8594 punct .,add

2_test

Id Subject Object Predicate Lexical cue
17590087-17030759-85657857 1151-1153 17030759 denotes 10
17590087-15623688-85657858 1154-1156 15623688 denotes 11
T92442 1151-1153 17030759 denotes 10
T77502 1154-1156 15623688 denotes 11