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Id Subject Object Predicate Lexical cue
T10397 0-7 RB denotes Perhaps
T10398 54-59 VBZ denotes stems
T10399 8-9 DT denotes a
T10400 22-33 NN denotes explanation
T10401 10-14 RBR denotes more
T10402 15-21 JJ denotes likely
T10403 34-37 IN denotes for
T10404 38-42 DT denotes this
T10405 43-53 NN denotes phenomenon
T10406 60-64 IN denotes from
T10407 65-77 JJ denotes experimental
T10408 78-90 NNS denotes observations
T10409 91-101 VBG denotes suggesting
T10410 102-106 IN denotes that
T10411 231-237 VB denotes escape
T10412 107-116 VBN denotes imprinted
T10413 119-131 NN denotes inactivation
T10414 117-118 NN denotes X
T10415 118-119 HYPH denotes -
T10416 139-146 VBN denotes imposed
T10417 132-134 VBZ denotes is
T10418 135-138 RB denotes not
T10419 147-149 IN denotes on
T10420 150-153 DT denotes all
T10421 154-164 NNS denotes precursors
T10422 165-167 IN denotes of
T10423 168-171 DT denotes the
T10424 193-200 NNS denotes tissues
T10425 172-177 NN denotes mouse
T10426 178-192 JJ denotes extraembryonic
T10427 200-202 : denotes :
T10428 202-203 DT denotes A
T10429 204-217 NN denotes subpopulation
T10430 218-220 IN denotes of
T10431 221-226 NNS denotes cells
T10432 227-230 MD denotes may
T10433 238-242 DT denotes this
T10434 243-250 NN denotes process
T10435 251-254 CC denotes and
T10436 255-259 VB denotes make
T10437 260-261 DT denotes a
T10438 270-276 NN denotes choice
T10439 262-268 JJ denotes random
T10440 269-270 `` denotes “
T10441 276-277 '' denotes ”
T10442 278-280 IN denotes of
T10443 281-286 WDT denotes which
T10444 289-299 NN denotes chromosome
T10445 287-288 NN denotes X
T10446 308-319 VBN denotes inactivated
T10447 300-304 MD denotes will
T10448 305-307 VB denotes be
T10449 319-320 . denotes .
T10450 320-448 sentence denotes On average, 50% of the cells in this randomly inactivating subpopulation would be expected to maintain an active Xp chromosome.
T10451 321-323 IN denotes On
T10452 403-411 VBN denotes expected
T10453 324-331 JJ denotes average
T10454 331-333 , denotes ,
T10455 333-335 CD denotes 50
T10456 335-336 NN denotes %
T10457 337-339 IN denotes of
T10458 340-343 DT denotes the
T10459 344-349 NNS denotes cells
T10460 350-352 IN denotes in
T10461 353-357 DT denotes this
T10462 380-393 NN denotes subpopulation
T10463 358-366 RB denotes randomly
T10464 367-379 VBG denotes inactivating
T10465 394-399 MD denotes would
T10466 400-402 VB denotes be
T10467 412-414 TO denotes to
T10468 415-423 VB denotes maintain
T10469 424-426 DT denotes an
T10470 437-447 NN denotes chromosome
T10471 427-433 JJ denotes active
T10472 434-436 NN denotes Xp
T10473 447-448 . denotes .
T10474 448-664 sentence denotes In support of this hypothesis, it has been demonstrated that expression of paternally transmitted X-linked lacZ [33,34] and GFP [35] transgenes failed to be silenced in a small subpopulation of extraembryonic cells.
T10475 449-451 IN denotes In
T10476 492-504 VBN denotes demonstrated
T10477 452-459 NN denotes support
T10478 460-462 IN denotes of
T10479 463-467 DT denotes this
T10480 468-478 NN denotes hypothesis
T10481 478-480 , denotes ,
T10482 480-482 PRP denotes it
T10483 483-486 VBZ denotes has
T10484 487-491 VBN denotes been
T10485 505-509 IN denotes that
T10486 593-599 VBD denotes failed
T10487 510-520 NN denotes expression
T10488 521-523 IN denotes of
T10489 524-534 RB denotes paternally
T10490 535-546 VBN denotes transmitted
T10491 556-560 NN denotes lacZ
T10492 547-548 NN denotes X
T10493 549-555 VBN denotes linked
T10494 548-549 HYPH denotes -
T10495 582-592 NNS denotes transgenes
T10496 561-562 -LRB- denotes [
T10497 565-567 CD denotes 34
T10498 562-564 CD denotes 33
T10499 564-565 , denotes ,
T10500 567-568 -RRB- denotes ]
T10501 569-572 CC denotes and
T10502 573-576 NN denotes GFP
T10503 577-578 -LRB- denotes [
T10504 578-580 CD denotes 35
T10505 580-581 -RRB- denotes ]
T10506 600-602 TO denotes to
T10507 606-614 VBN denotes silenced
T10508 603-605 VB denotes be
T10509 615-617 IN denotes in
T10510 618-619 DT denotes a
T10511 626-639 NN denotes subpopulation
T10512 620-625 JJ denotes small
T10513 640-642 IN denotes of
T10514 643-657 JJ denotes extraembryonic
T10515 658-663 NNS denotes cells
T10516 663-664 . denotes .
T10517 664-858 sentence denotes Further, it has been shown that in a subpopulation of extraembryonic cells, it is the Xm rather than the Xp that undergoes late replication, a molecular correlate of the inactive state [18,36].
T10518 665-672 RB denotes Further
T10519 686-691 VBN denotes shown
T10520 672-674 , denotes ,
T10521 674-676 PRP denotes it
T10522 677-680 VBZ denotes has
T10523 681-685 VBN denotes been
T10524 692-696 IN denotes that
T10525 744-746 VBZ denotes is
T10526 697-699 IN denotes in
T10527 700-701 DT denotes a
T10528 702-715 NN denotes subpopulation
T10529 716-718 IN denotes of
T10530 719-733 JJ denotes extraembryonic
T10531 734-739 NNS denotes cells
T10532 739-741 , denotes ,
T10533 741-743 PRP denotes it
T10534 747-750 DT denotes the
T10535 751-753 NN denotes Xm
T10536 754-760 JJ denotes rather
T10537 761-765 IN denotes than
T10538 766-769 DT denotes the
T10539 770-772 NN denotes Xp
T10540 773-777 WDT denotes that
T10541 778-787 VBZ denotes undergoes
T10542 788-792 JJ denotes late
T10543 793-804 NN denotes replication
T10544 804-806 , denotes ,
T10545 806-807 DT denotes a
T10546 818-827 NN denotes correlate
T10547 808-817 JJ denotes molecular
T10548 828-830 IN denotes of
T10549 831-834 DT denotes the
T10550 844-849 NN denotes state
T10551 835-843 JJ denotes inactive
T10552 850-851 -LRB- denotes [
T10553 854-856 CD denotes 36
T10554 851-853 CD denotes 18
T10555 853-854 , denotes ,
T10556 856-857 -RRB- denotes ]
T10557 857-858 . denotes .
T10558 858-1146 sentence denotes Although initially small and quickly diluted in normal embryos, the cellular subpopulation that inactivates the Xm chromosome could rapidly expand to replace the normally imprinted cells in extraembryonic lineages if the normal silencing of Xp compromises cell growth or differentiation.
T10559 859-867 IN denotes Although
T10560 878-883 JJ denotes small
T10561 868-877 RB denotes initially
T10562 999-1005 VB denotes expand
T10563 884-887 CC denotes and
T10564 888-895 RB denotes quickly
T10565 896-903 VBN denotes diluted
T10566 904-906 IN denotes in
T10567 907-913 JJ denotes normal
T10568 914-921 NNS denotes embryos
T10569 921-923 , denotes ,
T10570 923-926 DT denotes the
T10571 936-949 NN denotes subpopulation
T10572 927-935 JJ denotes cellular
T10573 950-954 WDT denotes that
T10574 955-966 VBZ denotes inactivates
T10575 967-970 DT denotes the
T10576 974-984 NN denotes chromosome
T10577 971-973 NN denotes Xm
T10578 985-990 MD denotes could
T10579 991-998 RB denotes rapidly
T10580 1006-1008 TO denotes to
T10581 1009-1016 VB denotes replace
T10582 1017-1020 DT denotes the
T10583 1040-1045 NNS denotes cells
T10584 1021-1029 RB denotes normally
T10585 1030-1039 VBN denotes imprinted
T10586 1046-1048 IN denotes in
T10587 1049-1063 JJ denotes extraembryonic
T10588 1064-1072 NNS denotes lineages
T10589 1073-1075 IN denotes if
T10590 1103-1114 VBZ denotes compromises
T10591 1076-1079 DT denotes the
T10592 1087-1096 NN denotes silencing
T10593 1080-1086 JJ denotes normal
T10594 1097-1099 IN denotes of
T10595 1100-1102 NN denotes Xp
T10596 1115-1119 NN denotes cell
T10597 1120-1126 NN denotes growth
T10598 1127-1129 CC denotes or
T10599 1130-1145 NN denotes differentiation
T10600 1145-1146 . denotes .
T10601 1146-1500 sentence denotes Interestingly, it has been suggested that the size of the population that initially escapes imprinting may range widely (from 0% to 30%), even between genetically identical embryos [37], and this may account for the variable phenotype observed among females bearing Xm-linked mutant alleles of genes essential for normal extraembryonic development [38].
T10602 1147-1160 RB denotes Interestingly
T10603 1174-1183 VBN denotes suggested
T10604 1160-1162 , denotes ,
T10605 1162-1164 PRP denotes it
T10606 1165-1168 VBZ denotes has
T10607 1169-1173 VBN denotes been
T10608 1184-1188 IN denotes that
T10609 1254-1259 VB denotes range
T10610 1189-1192 DT denotes the
T10611 1193-1197 NN denotes size
T10612 1198-1200 IN denotes of
T10613 1201-1204 DT denotes the
T10614 1205-1215 NN denotes population
T10615 1216-1220 WDT denotes that
T10616 1231-1238 VBZ denotes escapes
T10617 1221-1230 RB denotes initially
T10618 1239-1249 NN denotes imprinting
T10619 1250-1253 MD denotes may
T10620 1260-1266 RB denotes widely
T10621 1267-1268 -LRB- denotes (
T10622 1268-1272 IN denotes from
T10623 1273-1274 CD denotes 0
T10624 1274-1275 NN denotes %
T10625 1276-1278 IN denotes to
T10626 1279-1281 CD denotes 30
T10627 1281-1282 NN denotes %
T10628 1282-1283 -RRB- denotes )
T10629 1283-1285 , denotes ,
T10630 1285-1289 RB denotes even
T10631 1290-1297 IN denotes between
T10632 1298-1309 RB denotes genetically
T10633 1310-1319 JJ denotes identical
T10634 1320-1327 NNS denotes embryos
T10635 1328-1329 -LRB- denotes [
T10636 1329-1331 CD denotes 37
T10637 1331-1332 -RRB- denotes ]
T10638 1332-1334 , denotes ,
T10639 1334-1337 CC denotes and
T10640 1338-1342 DT denotes this
T10641 1347-1354 VB denotes account
T10642 1343-1346 MD denotes may
T10643 1355-1358 IN denotes for
T10644 1359-1362 DT denotes the
T10645 1372-1381 NN denotes phenotype
T10646 1363-1371 JJ denotes variable
T10647 1382-1390 VBN denotes observed
T10648 1391-1396 IN denotes among
T10649 1397-1404 NNS denotes females
T10650 1405-1412 VBG denotes bearing
T10651 1413-1415 NN denotes Xm
T10652 1416-1422 VBN denotes linked
T10653 1415-1416 HYPH denotes -
T10654 1430-1437 NNS denotes alleles
T10655 1423-1429 NN denotes mutant
T10656 1438-1440 IN denotes of
T10657 1441-1446 NNS denotes genes
T10658 1447-1456 JJ denotes essential
T10659 1457-1460 IN denotes for
T10660 1461-1467 JJ denotes normal
T10661 1483-1494 NN denotes development
T10662 1468-1482 JJ denotes extraembryonic
T10663 1495-1496 -LRB- denotes [
T10664 1496-1498 CD denotes 38
T10665 1498-1499 -RRB- denotes ]
T10666 1499-1500 . denotes .
T10667 1500-1653 sentence denotes Put simply, carrier females bearing a small initial population of escaping cells would be more severely affected than those bearing a larger population.
T10668 1501-1504 VBN denotes Put
T10669 1588-1590 VB denotes be
T10670 1505-1511 RB denotes simply
T10671 1511-1513 , denotes ,
T10672 1513-1520 NN denotes carrier
T10673 1521-1528 NNS denotes females
T10674 1529-1536 VBG denotes bearing
T10675 1537-1538 DT denotes a
T10676 1553-1563 NN denotes population
T10677 1539-1544 JJ denotes small
T10678 1545-1552 JJ denotes initial
T10679 1564-1566 IN denotes of
T10680 1567-1575 VBG denotes escaping
T10681 1576-1581 NNS denotes cells
T10682 1582-1587 MD denotes would
T10683 1591-1595 RBR denotes more
T10684 1596-1604 RB denotes severely
T10685 1605-1613 VBN denotes affected
T10686 1614-1618 IN denotes than
T10687 1619-1624 DT denotes those
T10688 1625-1632 VBG denotes bearing
T10689 1633-1634 DT denotes a
T10690 1642-1652 NN denotes population
T10691 1635-1641 JJR denotes larger
T10692 1652-1653 . denotes .
T10693 1653-1840 sentence denotes This could explain why we have observed significant phenotypic variation among Atrx carrier females, with some carriers dying in utero by 9.5 dpc (Table 1) and others developing to term.
T10694 1654-1658 DT denotes This
T10695 1665-1672 VB denotes explain
T10696 1659-1664 MD denotes could
T10697 1673-1676 WRB denotes why
T10698 1685-1693 VBN denotes observed
T10699 1677-1679 PRP denotes we
T10700 1680-1684 VBP denotes have
T10701 1694-1705 JJ denotes significant
T10702 1717-1726 NN denotes variation
T10703 1706-1716 JJ denotes phenotypic
T10704 1727-1732 IN denotes among
T10705 1733-1737 NN denotes Atrx
T10706 1738-1745 NN denotes carrier
T10707 1746-1753 NNS denotes females
T10708 1753-1755 , denotes ,
T10709 1755-1759 IN denotes with
T10710 1760-1764 DT denotes some
T10711 1765-1773 NNS denotes carriers
T10712 1774-1779 VBG denotes dying
T10713 1780-1782 FW denotes in
T10714 1783-1788 FW denotes utero
T10715 1789-1791 IN denotes by
T10716 1792-1795 CD denotes 9.5
T10717 1796-1799 NNS denotes dpc
T10718 1800-1801 -LRB- denotes (
T10719 1801-1806 NN denotes Table
T10720 1807-1808 CD denotes 1
T10721 1808-1809 -RRB- denotes )
T10722 1810-1813 CC denotes and
T10723 1814-1820 NNS denotes others
T10724 1821-1831 VBG denotes developing
T10725 1832-1834 IN denotes to
T10726 1835-1839 NN denotes term
T10727 1839-1840 . denotes .
R6366 T10397 T10398 advmod Perhaps,stems
R6367 T10399 T10400 det a,explanation
R6368 T10400 T10398 nsubj explanation,stems
R6369 T10401 T10402 advmod more,likely
R6370 T10402 T10400 amod likely,explanation
R6371 T10403 T10400 prep for,explanation
R6372 T10404 T10405 det this,phenomenon
R6373 T10405 T10403 pobj phenomenon,for
R6374 T10406 T10398 prep from,stems
R6375 T10407 T10408 amod experimental,observations
R6376 T10408 T10406 pobj observations,from
R6377 T10409 T10408 acl suggesting,observations
R6378 T10410 T10411 mark that,escape
R6379 T10411 T10409 ccomp escape,suggesting
R6380 T10412 T10413 amod imprinted,inactivation
R6381 T10413 T10416 nsubjpass inactivation,imposed
R6382 T10414 T10413 compound X,inactivation
R6383 T10415 T10413 punct -,inactivation
R6384 T10416 T10411 ccomp imposed,escape
R6385 T10417 T10416 auxpass is,imposed
R6386 T10418 T10416 neg not,imposed
R6387 T10419 T10416 prep on,imposed
R6388 T10420 T10421 det all,precursors
R6389 T10421 T10419 pobj precursors,on
R6390 T10422 T10421 prep of,precursors
R6391 T10423 T10424 det the,tissues
R6392 T10424 T10422 pobj tissues,of
R6393 T10425 T10424 nmod mouse,tissues
R6394 T10426 T10425 amod extraembryonic,mouse
R6395 T10427 T10411 punct : ,escape
R6396 T10428 T10429 det A,subpopulation
R6397 T10429 T10411 nsubj subpopulation,escape
R6398 T10430 T10429 prep of,subpopulation
R6399 T10431 T10430 pobj cells,of
R6400 T10432 T10411 aux may,escape
R6401 T10433 T10434 det this,process
R6402 T10434 T10411 dobj process,escape
R6403 T10435 T10411 cc and,escape
R6404 T10436 T10411 conj make,escape
R6405 T10437 T10438 det a,choice
R6406 T10438 T10436 dobj choice,make
R6407 T10439 T10438 amod random,choice
R6408 T10440 T10438 punct “,choice
R6409 T10441 T10438 punct ”,choice
R6410 T10442 T10438 prep of,choice
R6411 T10443 T10444 det which,chromosome
R6412 T10444 T10446 dep chromosome,inactivated
R6413 T10445 T10444 compound X,chromosome
R6414 T10446 T10442 pcomp inactivated,of
R6415 T10447 T10446 aux will,inactivated
R6416 T10448 T10446 auxpass be,inactivated
R6417 T10449 T10398 punct .,stems
R6418 T10451 T10452 prep On,expected
R6419 T10453 T10451 amod average,On
R6420 T10454 T10452 punct ", ",expected
R6421 T10455 T10456 nummod 50,%
R6422 T10456 T10452 nsubjpass %,expected
R6423 T10457 T10456 prep of,%
R6424 T10458 T10459 det the,cells
R6425 T10459 T10457 pobj cells,of
R6426 T10460 T10456 prep in,%
R6427 T10461 T10462 det this,subpopulation
R6428 T10462 T10460 pobj subpopulation,in
R6429 T10463 T10464 advmod randomly,inactivating
R6430 T10464 T10462 amod inactivating,subpopulation
R6431 T10465 T10452 aux would,expected
R6432 T10466 T10452 auxpass be,expected
R6433 T10467 T10468 aux to,maintain
R6434 T10468 T10452 xcomp maintain,expected
R6435 T10469 T10470 det an,chromosome
R6436 T10470 T10468 dobj chromosome,maintain
R6437 T10471 T10470 amod active,chromosome
R6438 T10472 T10470 compound Xp,chromosome
R6439 T10473 T10452 punct .,expected
R6440 T10475 T10476 prep In,demonstrated
R6441 T10477 T10475 pobj support,In
R6442 T10478 T10477 prep of,support
R6443 T10479 T10480 det this,hypothesis
R6444 T10480 T10478 pobj hypothesis,of
R6445 T10481 T10476 punct ", ",demonstrated
R6446 T10482 T10476 nsubjpass it,demonstrated
R6447 T10483 T10476 aux has,demonstrated
R6448 T10484 T10476 auxpass been,demonstrated
R6449 T10485 T10486 mark that,failed
R6450 T10486 T10476 ccomp failed,demonstrated
R6451 T10487 T10486 nsubj expression,failed
R6452 T10488 T10487 prep of,expression
R6453 T10489 T10490 advmod paternally,transmitted
R6454 T10490 T10491 amod transmitted,lacZ
R6455 T10491 T10495 nmod lacZ,transgenes
R6456 T10492 T10493 npadvmod X,linked
R6457 T10493 T10491 amod linked,lacZ
R6458 T10494 T10493 punct -,linked
R6459 T10495 T10488 pobj transgenes,of
R6460 T10496 T10497 punct [,34
R6461 T10497 T10491 parataxis 34,lacZ
R6462 T10498 T10497 nummod 33,34
R6463 T10499 T10497 punct ",",34
R6464 T10500 T10497 punct ],34
R6465 T10501 T10491 cc and,lacZ
R6466 T10502 T10491 conj GFP,lacZ
R6467 T10503 T10504 punct [,35
R6468 T10504 T10502 parataxis 35,GFP
R6469 T10505 T10504 punct ],35
R6470 T10506 T10507 aux to,silenced
R6471 T10507 T10486 xcomp silenced,failed
R6472 T10508 T10507 auxpass be,silenced
R6473 T10509 T10507 prep in,silenced
R6474 T10510 T10511 det a,subpopulation
R6475 T10511 T10509 pobj subpopulation,in
R6476 T10512 T10511 amod small,subpopulation
R6477 T10513 T10511 prep of,subpopulation
R6478 T10514 T10515 amod extraembryonic,cells
R6479 T10515 T10513 pobj cells,of
R6480 T10516 T10476 punct .,demonstrated
R6481 T10518 T10519 advmod Further,shown
R6482 T10520 T10519 punct ", ",shown
R6483 T10521 T10519 nsubjpass it,shown
R6484 T10522 T10519 aux has,shown
R6485 T10523 T10519 auxpass been,shown
R6486 T10524 T10525 mark that,is
R6487 T10525 T10519 ccomp is,shown
R6488 T10526 T10525 prep in,is
R6489 T10527 T10528 det a,subpopulation
R6490 T10528 T10526 pobj subpopulation,in
R6491 T10529 T10528 prep of,subpopulation
R6492 T10530 T10531 amod extraembryonic,cells
R6493 T10531 T10529 pobj cells,of
R6494 T10532 T10525 punct ", ",is
R6495 T10533 T10525 nsubj it,is
R6496 T10534 T10535 det the,Xm
R6497 T10535 T10525 attr Xm,is
R6498 T10536 T10537 amod rather,than
R6499 T10537 T10535 cc than,Xm
R6500 T10538 T10539 det the,Xp
R6501 T10539 T10535 conj Xp,Xm
R6502 T10540 T10541 dep that,undergoes
R6503 T10541 T10535 relcl undergoes,Xm
R6504 T10542 T10543 amod late,replication
R6505 T10543 T10541 dobj replication,undergoes
R6506 T10544 T10543 punct ", ",replication
R6507 T10545 T10546 det a,correlate
R6508 T10546 T10543 appos correlate,replication
R6509 T10547 T10546 amod molecular,correlate
R6510 T10548 T10546 prep of,correlate
R6511 T10549 T10550 det the,state
R6512 T10550 T10548 pobj state,of
R6513 T10551 T10550 amod inactive,state
R6514 T10552 T10553 punct [,36
R6515 T10553 T10525 parataxis 36,is
R6516 T10554 T10553 nummod 18,36
R6517 T10555 T10553 punct ",",36
R6518 T10556 T10553 punct ],36
R6519 T10557 T10519 punct .,shown
R6520 T10559 T10560 mark Although,small
R6521 T10560 T10562 advcl small,expand
R6522 T10561 T10560 advmod initially,small
R6523 T10563 T10560 cc and,small
R6524 T10564 T10565 advmod quickly,diluted
R6525 T10565 T10560 conj diluted,small
R6526 T10566 T10565 prep in,diluted
R6527 T10567 T10568 amod normal,embryos
R6528 T10568 T10566 pobj embryos,in
R6529 T10569 T10562 punct ", ",expand
R6530 T10570 T10571 det the,subpopulation
R6531 T10571 T10562 nsubj subpopulation,expand
R6532 T10572 T10571 amod cellular,subpopulation
R6533 T10573 T10574 dep that,inactivates
R6534 T10574 T10571 relcl inactivates,subpopulation
R6535 T10575 T10576 det the,chromosome
R6536 T10576 T10574 dobj chromosome,inactivates
R6537 T10577 T10576 compound Xm,chromosome
R6538 T10578 T10562 aux could,expand
R6539 T10579 T10562 advmod rapidly,expand
R6540 T10580 T10581 aux to,replace
R6541 T10581 T10562 advcl replace,expand
R6542 T10582 T10583 det the,cells
R6543 T10583 T10581 dobj cells,replace
R6544 T10584 T10585 advmod normally,imprinted
R6545 T10585 T10583 amod imprinted,cells
R6546 T10586 T10583 prep in,cells
R6547 T10587 T10588 amod extraembryonic,lineages
R6548 T10588 T10586 pobj lineages,in
R6549 T10589 T10590 mark if,compromises
R6550 T10590 T10562 advcl compromises,expand
R6551 T10591 T10592 det the,silencing
R6552 T10592 T10590 nsubj silencing,compromises
R6553 T10593 T10592 amod normal,silencing
R6554 T10594 T10592 prep of,silencing
R6555 T10595 T10594 pobj Xp,of
R6556 T10596 T10597 compound cell,growth
R6557 T10597 T10590 dobj growth,compromises
R6558 T10598 T10597 cc or,growth
R6559 T10599 T10597 conj differentiation,growth
R6560 T10600 T10562 punct .,expand
R6561 T10602 T10603 advmod Interestingly,suggested
R6562 T10604 T10603 punct ", ",suggested
R6563 T10605 T10603 nsubjpass it,suggested
R6564 T10606 T10603 aux has,suggested
R6565 T10607 T10603 auxpass been,suggested
R6566 T10608 T10609 mark that,range
R6567 T10609 T10603 ccomp range,suggested
R6568 T10610 T10611 det the,size
R6569 T10611 T10609 nsubj size,range
R6570 T10612 T10611 prep of,size
R6571 T10613 T10614 det the,population
R6572 T10614 T10612 pobj population,of
R6573 T10615 T10616 dep that,escapes
R6574 T10616 T10614 relcl escapes,population
R6575 T10617 T10616 advmod initially,escapes
R6576 T10618 T10616 dobj imprinting,escapes
R6577 T10619 T10609 aux may,range
R6578 T10620 T10609 advmod widely,range
R6579 T10621 T10609 punct (,range
R6580 T10622 T10609 prep from,range
R6581 T10623 T10624 nummod 0,%
R6582 T10624 T10622 pobj %,from
R6583 T10625 T10622 prep to,from
R6584 T10626 T10627 nummod 30,%
R6585 T10627 T10625 pobj %,to
R6586 T10628 T10609 punct ),range
R6587 T10629 T10609 punct ", ",range
R6588 T10630 T10631 advmod even,between
R6589 T10631 T10609 prep between,range
R6590 T10632 T10633 advmod genetically,identical
R6591 T10633 T10634 amod identical,embryos
R6592 T10634 T10631 pobj embryos,between
R6593 T10635 T10636 punct [,37
R6594 T10636 T10609 parataxis 37,range
R6595 T10637 T10636 punct ],37
R6596 T10638 T10603 punct ", ",suggested
R6597 T10639 T10603 cc and,suggested
R6598 T10640 T10641 nsubj this,account
R6599 T10641 T10603 conj account,suggested
R6600 T10642 T10641 aux may,account
R6601 T10643 T10641 prep for,account
R6602 T10644 T10645 det the,phenotype
R6603 T10645 T10643 pobj phenotype,for
R6604 T10646 T10645 amod variable,phenotype
R6605 T10647 T10645 acl observed,phenotype
R6606 T10648 T10647 prep among,observed
R6607 T10649 T10648 pobj females,among
R6608 T10650 T10649 acl bearing,females
R6609 T10651 T10652 npadvmod Xm,linked
R6610 T10652 T10654 amod linked,alleles
R6611 T10653 T10652 punct -,linked
R6612 T10654 T10650 dobj alleles,bearing
R6613 T10655 T10654 compound mutant,alleles
R6614 T10656 T10654 prep of,alleles
R6615 T10657 T10656 pobj genes,of
R6616 T10658 T10657 amod essential,genes
R6617 T10659 T10658 prep for,essential
R6618 T10660 T10661 amod normal,development
R6619 T10661 T10659 pobj development,for
R6620 T10662 T10661 amod extraembryonic,development
R6621 T10663 T10664 punct [,38
R6622 T10664 T10641 parataxis 38,account
R6623 T10665 T10664 punct ],38
R6624 T10666 T10641 punct .,account
R6625 T10668 T10669 advcl Put,be
R6626 T10670 T10668 advmod simply,Put
R6627 T10671 T10669 punct ", ",be
R6628 T10672 T10673 compound carrier,females
R6629 T10673 T10669 nsubj females,be
R6630 T10674 T10673 acl bearing,females
R6631 T10675 T10676 det a,population
R6632 T10676 T10674 dobj population,bearing
R6633 T10677 T10676 amod small,population
R6634 T10678 T10676 amod initial,population
R6635 T10679 T10676 prep of,population
R6636 T10680 T10681 amod escaping,cells
R6637 T10681 T10679 pobj cells,of
R6638 T10682 T10669 aux would,be
R6639 T10683 T10684 advmod more,severely
R6640 T10684 T10685 advmod severely,affected
R6641 T10685 T10669 acomp affected,be
R6642 T10686 T10685 prep than,affected
R6643 T10687 T10686 pobj those,than
R6644 T10688 T10687 acl bearing,those
R6645 T10689 T10690 det a,population
R6646 T10690 T10688 dobj population,bearing
R6647 T10691 T10690 amod larger,population
R6648 T10692 T10669 punct .,be
R6649 T10694 T10695 nsubj This,explain
R6650 T10696 T10695 aux could,explain
R6651 T10697 T10698 advmod why,observed
R6652 T10698 T10695 ccomp observed,explain
R6653 T10699 T10698 nsubj we,observed
R6654 T10700 T10698 aux have,observed
R6655 T10701 T10702 amod significant,variation
R6656 T10702 T10698 dobj variation,observed
R6657 T10703 T10702 amod phenotypic,variation
R6658 T10704 T10702 prep among,variation
R6659 T10705 T10706 compound Atrx,carrier
R6660 T10706 T10707 compound carrier,females
R6661 T10707 T10704 pobj females,among
R6662 T10708 T10698 punct ", ",observed
R6663 T10709 T10698 prep with,observed
R6664 T10710 T10711 det some,carriers
R6665 T10711 T10712 nsubj carriers,dying
R6666 T10712 T10709 pobj dying,with
R6667 T10713 T10714 advmod in,utero
R6668 T10714 T10712 advmod utero,dying
R6669 T10715 T10712 prep by,dying
R6670 T10716 T10717 nummod 9.5,dpc
R6671 T10717 T10715 pobj dpc,by
R6672 T10718 T10719 punct (,Table
R6673 T10719 T10712 parataxis Table,dying
R6674 T10720 T10719 nummod 1,Table
R6675 T10721 T10719 punct ),Table
R6676 T10722 T10712 cc and,dying
R6677 T10723 T10724 nsubj others,developing
R6678 T10724 T10712 conj developing,dying
R6679 T10725 T10724 prep to,developing
R6680 T10726 T10725 pobj term,to
R6681 T10727 T10695 punct .,explain

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
T9854 107-131 GO:0060819 denotes imprinted X-inactivation
T9855 117-118 GO:0000805 denotes X
T9856 172-177 NCBITaxon:10088 denotes mouse
T9857 178-200 UBERON:0005292 denotes extraembryonic tissues
T9858 207-226 UBERON_EXT:cell_clump_or_cluster_or_group_or_mass_or_population denotes population of cells
T9859 221-226 CL_GO_EXT:cell denotes cells
T9860 287-299 GO:0000805 denotes X chromosome
T9861 289-299 GO_SO_EXT:chromosome denotes chromosome
T9862 344-349 CL_GO_EXT:cell denotes cells
T9863 437-447 GO_SO_EXT:chromosome denotes chromosome
T9864 510-520 GO:0010467 denotes expression
T9865 547-548 GO:0000805 denotes X
T9866 556-560 PR_EXT:000033987 denotes lacZ
T9867 582-592 SO_EXT:0000902 denotes transgenes
T9868 606-614 GO:0016458 denotes silenced
T9869 629-642 _FRAGMENT denotes population of
T9870 658-663 UBERON_EXT:cell_clump_or_cluster_or_group_or_mass_or_population denotes cells
T9871 643-663 CL:0000349 denotes extraembryonic cells
T9872 648-657 UBERON:0000922 denotes embryonic
T9873 658-663 CL_GO_EXT:cell denotes cells
T9874 705-718 _FRAGMENT denotes population of
T9875 734-739 UBERON_EXT:cell_clump_or_cluster_or_group_or_mass_or_population denotes cells
T9876 719-739 CL:0000349 denotes extraembryonic cells
T9877 724-733 UBERON:0000922 denotes embryonic
T9878 734-739 CL_GO_EXT:cell denotes cells
T9879 793-804 GO:0006260 denotes replication
T9880 808-817 CHEBI_EXT:polyatomic_entity_or_group denotes molecular
T9881 914-921 UBERON:0000922 denotes embryos
T9882 927-935 CL_GO_EXT:cell denotes cellular
T9883 927-935 _FRAGMENT denotes cellular
T9884 939-949 UBERON_EXT:cell_clump_or_cluster_or_group_or_mass_or_population denotes population
T9885 974-984 GO_SO_EXT:chromosome denotes chromosome
T9886 1030-1039 GO:0071514 denotes imprinted
T9887 1040-1045 CL_GO_EXT:cell denotes cells
T9888 1054-1063 UBERON:0000922 denotes embryonic
T9889 1087-1096 GO:0016458 denotes silencing
T9890 1115-1119 CL_GO_EXT:cell denotes cell
T9891 1115-1119 _FRAGMENT denotes cell
T9892 1130-1145 GO:0030154 denotes differentiation
T9893 1120-1126 GO_EXT:biological_growth_entity_or_process denotes growth
T9894 1239-1249 GO:0071514 denotes imprinting
T9895 1298-1309 SO_EXT:0000704 denotes genetically
T9896 1320-1327 UBERON:0000922 denotes embryos
T9897 1397-1404 PATO_UBERON_EXT:female_or_bearer_of_femaleness denotes females
T9898 1423-1429 SO_EXT:sequence_altered_entity_or_alteration_process denotes mutant
T9899 1430-1437 SO_EXT:0001023 denotes alleles
T9900 1441-1446 SO_EXT:0000704 denotes genes
T9901 1473-1482 UBERON:0000922 denotes embryonic
T9902 1521-1528 PATO_UBERON_EXT:female_or_bearer_of_femaleness denotes females
T9903 1553-1566 _FRAGMENT denotes population of
T9904 1576-1581 UBERON_EXT:cell_clump_or_cluster_or_group_or_mass_or_population denotes cells
T9905 1576-1581 CL_GO_EXT:cell denotes cells
T9906 1733-1737 PR_EXT:000004503 denotes Atrx
T9907 1746-1753 PATO_UBERON_EXT:female_or_bearer_of_femaleness denotes females
T9908 1774-1779 GO:0016265 denotes dying
R5920 T9870 T9869 _lexicallyChainedTo cells,population of
R5921 T9875 T9874 _lexicallyChainedTo cells,population of
R5922 T9884 T9883 _lexicallyChainedTo population,cellular
R5923 T9892 T9891 _lexicallyChainedTo differentiation,cell
R5924 T9904 T9903 _lexicallyChainedTo cells,population of

2_test

Id Subject Object Predicate Lexical cue
16628246-7834909-85799776 562-564 7834909 denotes 33
16628246-10794075-85799777 565-567 10794075 denotes 34
16628246-11252054-85799778 578-580 11252054 denotes 35
16628246-1152998-85799779 851-853 1152998 denotes 18
16628246-958416-85799780 854-856 958416 denotes 36
16628246-11698184-85799781 1329-1331 11698184 denotes 37
16628246-11051544-85799782 1496-1498 11051544 denotes 38
T81121 562-564 7834909 denotes 33
T60587 565-567 10794075 denotes 34
T75568 578-580 11252054 denotes 35
T99758 851-853 1152998 denotes 18
T9314 854-856 958416 denotes 36
T45193 1329-1331 11698184 denotes 37
T45487 1496-1498 11051544 denotes 38

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
T9681 107-131 GO:0060819 denotes imprinted X-inactivation
T9682 117-118 GO:0000805 denotes X
T9683 172-177 NCBITaxon:10088 denotes mouse
T9684 178-200 UBERON:0005292 denotes extraembryonic tissues
T9685 287-299 GO:0000805 denotes X chromosome
T9686 510-520 GO:0010467 denotes expression
T9687 547-548 GO:0000805 denotes X
T9688 556-560 PR:000033987 denotes lacZ
T9689 582-592 SO:0000902 denotes transgenes
T9690 606-614 GO:0016458 denotes silenced
T9691 643-663 CL:0000349 denotes extraembryonic cells
T9692 648-657 UBERON:0000922 denotes embryonic
T9693 719-739 CL:0000349 denotes extraembryonic cells
T9694 724-733 UBERON:0000922 denotes embryonic
T9695 793-804 GO:0006260 denotes replication
T9696 914-921 UBERON:0000922 denotes embryos
T9697 1030-1039 GO:0071514 denotes imprinted
T9698 1054-1063 UBERON:0000922 denotes embryonic
T9699 1087-1096 GO:0016458 denotes silencing
T9700 1115-1119 _FRAGMENT denotes cell
T9701 1130-1145 GO:0030154 denotes differentiation
T9702 1239-1249 GO:0071514 denotes imprinting
T9703 1298-1309 SO:0000704 denotes genetically
T9704 1320-1327 UBERON:0000922 denotes embryos
T9705 1430-1437 SO:0001023 denotes alleles
T9706 1441-1446 SO:0000704 denotes genes
T9707 1473-1482 UBERON:0000922 denotes embryonic
T9708 1733-1737 PR:000004503 denotes Atrx
T9709 1774-1779 GO:0016265 denotes dying
R5915 T9701 T9700 _lexicallyChainedTo differentiation,cell