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PMC:1482699 / 35491-37158 JSONTXT

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Id Subject Object Predicate Lexical cue
T21607 0-11 NN denotes Development
T21608 12-14 IN denotes of
T21609 15-22 NN denotes B6.CAST
T21610 35-39 NN denotes MMU2
T21611 23-26 CC denotes and
T21612 27-34 NN denotes HG.CAST
T21613 55-62 NNS denotes strains
T21614 40-45 NN denotes speed
T21615 46-54 JJ denotes congenic
T21616 62-188 sentence denotes All speed congenic strains were developed starting with an initial cross between a CAST male and HG females (Figure 1) [5,6].
T21617 63-66 DT denotes All
T21618 82-89 NNS denotes strains
T21619 67-72 NN denotes speed
T21620 73-81 JJ denotes congenic
T21621 95-104 VBN denotes developed
T21622 90-94 VBD denotes were
T21623 105-113 VBG denotes starting
T21624 114-118 IN denotes with
T21625 119-121 DT denotes an
T21626 130-135 NN denotes cross
T21627 122-129 JJ denotes initial
T21628 136-143 IN denotes between
T21629 144-145 DT denotes a
T21630 151-155 NN denotes male
T21631 146-150 NN denotes CAST
T21632 156-159 CC denotes and
T21633 160-162 NN denotes HG
T21634 163-170 NNS denotes females
T21635 171-172 -LRB- denotes (
T21636 172-178 NN denotes Figure
T21637 179-180 CD denotes 1
T21638 180-181 -RRB- denotes )
T21639 182-183 -LRB- denotes [
T21640 185-186 CD denotes 6
T21641 183-184 CD denotes 5
T21642 184-185 , denotes ,
T21643 186-187 -RRB- denotes ]
T21644 187-188 . denotes .
T21645 188-238 sentence denotes Male F1 mice were then backcrossed to HG females.
T21646 189-193 JJ denotes Male
T21647 197-201 NNS denotes mice
T21648 194-196 NN denotes F1
T21649 212-223 VBN denotes backcrossed
T21650 202-206 VBD denotes were
T21651 207-211 RB denotes then
T21652 224-226 IN denotes to
T21653 227-229 NN denotes HG
T21654 230-237 NNS denotes females
T21655 237-238 . denotes .
T21656 238-391 sentence denotes All agouti (the dominant nonagouti (a) locus is located at 154.8 Mbp on MMU2) N2 males were genotyped for 79 microsatellite markers (Additional File 1).
T21657 239-242 DT denotes All
T21658 320-325 NNS denotes males
T21659 243-249 NN denotes agouti
T21660 250-251 -LRB- denotes (
T21661 287-294 VBN denotes located
T21662 251-254 DT denotes the
T21663 278-283 NN denotes locus
T21664 255-263 JJ denotes dominant
T21665 264-273 JJ denotes nonagouti
T21666 275-276 NN denotes a
T21667 274-275 -LRB- denotes (
T21668 276-277 -RRB- denotes )
T21669 284-286 VBZ denotes is
T21670 295-297 IN denotes at
T21671 298-303 CD denotes 154.8
T21672 304-307 NN denotes Mbp
T21673 308-310 IN denotes on
T21674 311-315 NN denotes MMU2
T21675 315-316 -RRB- denotes )
T21676 317-319 NN denotes N2
T21677 331-340 VBN denotes genotyped
T21678 326-330 VBD denotes were
T21679 341-344 IN denotes for
T21680 345-347 CD denotes 79
T21681 363-370 NNS denotes markers
T21682 348-362 NN denotes microsatellite
T21683 371-372 -LRB- denotes (
T21684 383-387 NN denotes File
T21685 372-382 JJ denotes Additional
T21686 388-389 CD denotes 1
T21687 389-390 -RRB- denotes )
T21688 390-391 . denotes .
T21689 391-539 sentence denotes These markers were evenly spaced across the genome, except in regions previously identified as harboring QTL [1], which were more densely screened.
T21690 392-397 DT denotes These
T21691 398-405 NNS denotes markers
T21692 418-424 VBN denotes spaced
T21693 406-410 VBD denotes were
T21694 411-417 RB denotes evenly
T21695 425-431 IN denotes across
T21696 432-435 DT denotes the
T21697 436-442 NN denotes genome
T21698 442-444 , denotes ,
T21699 444-450 RB denotes except
T21700 451-453 IN denotes in
T21701 454-461 NNS denotes regions
T21702 462-472 RB denotes previously
T21703 473-483 VBN denotes identified
T21704 484-486 IN denotes as
T21705 487-496 VBG denotes harboring
T21706 497-500 NN denotes QTL
T21707 501-502 -LRB- denotes [
T21708 502-503 CD denotes 1
T21709 503-504 -RRB- denotes ]
T21710 504-506 , denotes ,
T21711 506-511 WDT denotes which
T21712 530-538 VBN denotes screened
T21713 512-516 VBD denotes were
T21714 517-521 RBR denotes more
T21715 522-529 RB denotes densely
T21716 538-539 . denotes .
T21717 539-705 sentence denotes The "best" N2 agouti male with the lowest level of genome-wide unwanted heterozygosity while maintaining CAST alleles for all MMU2 markers was selected for breeding.
T21718 540-543 DT denotes The
T21719 561-565 NN denotes male
T21720 544-545 `` denotes "
T21721 545-549 JJS denotes best
T21722 549-550 '' denotes "
T21723 551-553 NN denotes N2
T21724 554-560 NN denotes agouti
T21725 683-691 VBN denotes selected
T21726 566-570 IN denotes with
T21727 571-574 DT denotes the
T21728 582-587 NN denotes level
T21729 575-581 JJS denotes lowest
T21730 588-590 IN denotes of
T21731 591-597 NN denotes genome
T21732 598-602 JJ denotes wide
T21733 597-598 HYPH denotes -
T21734 612-626 NN denotes heterozygosity
T21735 603-611 JJ denotes unwanted
T21736 627-632 IN denotes while
T21737 633-644 VBG denotes maintaining
T21738 645-649 NN denotes CAST
T21739 650-657 NNS denotes alleles
T21740 658-661 IN denotes for
T21741 662-665 DT denotes all
T21742 671-678 NNS denotes markers
T21743 666-670 NN denotes MMU2
T21744 679-682 VBD denotes was
T21745 692-695 IN denotes for
T21746 696-704 NN denotes breeding
T21747 704-705 . denotes .
T21748 705-839 sentence denotes This selection scheme was used at each generation until a N4 male was identified as homozygous HG for all markers typed outside MMU2.
T21749 706-710 DT denotes This
T21750 721-727 NN denotes scheme
T21751 711-720 NN denotes selection
T21752 732-736 VBN denotes used
T21753 728-731 VBD denotes was
T21754 737-739 IN denotes at
T21755 740-744 DT denotes each
T21756 745-755 NN denotes generation
T21757 756-761 IN denotes until
T21758 776-786 VBN denotes identified
T21759 762-763 DT denotes a
T21760 767-771 NN denotes male
T21761 764-766 NN denotes N4
T21762 772-775 VBD denotes was
T21763 787-789 IN denotes as
T21764 790-800 JJ denotes homozygous
T21765 801-803 NN denotes HG
T21766 804-807 IN denotes for
T21767 808-811 DT denotes all
T21768 812-819 NNS denotes markers
T21769 820-825 VBN denotes typed
T21770 826-833 IN denotes outside
T21771 834-838 NN denotes MMU2
T21772 838-839 . denotes .
T21773 839-983 sentence denotes After an additional backcross to HG females, recombinant males were identified providing the foundation for the four overlapping donor regions.
T21774 840-845 IN denotes After
T21775 908-918 VBN denotes identified
T21776 846-848 DT denotes an
T21777 860-869 NN denotes backcross
T21778 849-859 JJ denotes additional
T21779 870-872 IN denotes to
T21780 873-875 NN denotes HG
T21781 876-883 NNS denotes females
T21782 883-885 , denotes ,
T21783 885-896 JJ denotes recombinant
T21784 897-902 NNS denotes males
T21785 903-907 VBD denotes were
T21786 919-928 VBG denotes providing
T21787 929-932 DT denotes the
T21788 933-943 NN denotes foundation
T21789 944-947 IN denotes for
T21790 948-951 DT denotes the
T21791 975-982 NNS denotes regions
T21792 952-956 CD denotes four
T21793 957-968 VBG denotes overlapping
T21794 969-974 NN denotes donor
T21795 982-983 . denotes .
T21796 983-1138 sentence denotes Selected recombinant males were then backcrossed to both B6 and HG females to create strains, which were B6 (+/+) or HG (hg/hg) and heterozygous congenic.
T21797 984-992 VBN denotes Selected
T21798 1005-1010 NNS denotes males
T21799 993-1004 JJ denotes recombinant
T21800 1021-1032 VBN denotes backcrossed
T21801 1011-1015 VBD denotes were
T21802 1016-1020 RB denotes then
T21803 1033-1035 IN denotes to
T21804 1036-1040 CC denotes both
T21805 1041-1043 NN denotes B6
T21806 1051-1058 NNS denotes females
T21807 1044-1047 CC denotes and
T21808 1048-1050 NN denotes HG
T21809 1059-1061 TO denotes to
T21810 1062-1068 VB denotes create
T21811 1069-1076 NNS denotes strains
T21812 1076-1078 , denotes ,
T21813 1078-1083 WDT denotes which
T21814 1084-1088 VBD denotes were
T21815 1089-1091 NN denotes B6
T21816 1129-1137 JJ denotes congenic
T21817 1092-1093 -LRB- denotes (
T21818 1095-1096 SYM denotes +
T21819 1093-1094 SYM denotes +
T21820 1094-1095 HYPH denotes /
T21821 1096-1097 -RRB- denotes )
T21822 1098-1100 CC denotes or
T21823 1101-1103 NN denotes HG
T21824 1104-1105 -LRB- denotes (
T21825 1108-1110 NN denotes hg
T21826 1105-1107 NN denotes hg
T21827 1107-1108 HYPH denotes /
T21828 1110-1111 -RRB- denotes )
T21829 1112-1115 CC denotes and
T21830 1116-1128 JJ denotes heterozygous
T21831 1137-1138 . denotes .
T21832 1138-1213 sentence denotes These mice were intermated to produce homozygous founders for each strain.
T21833 1139-1144 DT denotes These
T21834 1145-1149 NNS denotes mice
T21835 1155-1165 VBN denotes intermated
T21836 1150-1154 VBD denotes were
T21837 1166-1168 TO denotes to
T21838 1169-1176 VB denotes produce
T21839 1177-1187 JJ denotes homozygous
T21840 1188-1196 NNS denotes founders
T21841 1197-1200 IN denotes for
T21842 1201-1205 DT denotes each
T21843 1206-1212 NN denotes strain
T21844 1212-1213 . denotes .
T21845 1213-1427 sentence denotes This novel breeding scheme created four identical founder congenics on two backgrounds B6 (+/+) and HG (hg/hg), which formed the basis for our examination of interactions caused by the presence of the hg deletion.
T21846 1214-1218 DT denotes This
T21847 1234-1240 NN denotes scheme
T21848 1219-1224 JJ denotes novel
T21849 1225-1233 VBG denotes breeding
T21850 1241-1248 VBD denotes created
T21851 1249-1253 CD denotes four
T21852 1272-1281 NNS denotes congenics
T21853 1254-1263 JJ denotes identical
T21854 1264-1271 NN denotes founder
T21855 1282-1284 IN denotes on
T21856 1285-1288 CD denotes two
T21857 1289-1300 NNS denotes backgrounds
T21858 1301-1303 NN denotes B6
T21859 1304-1305 -LRB- denotes (
T21860 1307-1308 SYM denotes +
T21861 1305-1306 SYM denotes +
T21862 1306-1307 HYPH denotes /
T21863 1308-1309 -RRB- denotes )
T21864 1310-1313 CC denotes and
T21865 1314-1316 NN denotes HG
T21866 1317-1318 -LRB- denotes (
T21867 1321-1323 NN denotes hg
T21868 1318-1320 NN denotes hg
T21869 1320-1321 HYPH denotes /
T21870 1323-1324 -RRB- denotes )
T21871 1324-1326 , denotes ,
T21872 1326-1331 WDT denotes which
T21873 1332-1338 VBD denotes formed
T21874 1339-1342 DT denotes the
T21875 1343-1348 NN denotes basis
T21876 1349-1352 IN denotes for
T21877 1353-1356 PRP$ denotes our
T21878 1357-1368 NN denotes examination
T21879 1369-1371 IN denotes of
T21880 1372-1384 NNS denotes interactions
T21881 1385-1391 VBN denotes caused
T21882 1392-1394 IN denotes by
T21883 1395-1398 DT denotes the
T21884 1399-1407 NN denotes presence
T21885 1408-1410 IN denotes of
T21886 1411-1414 DT denotes the
T21887 1418-1426 NN denotes deletion
T21888 1415-1417 NN denotes hg
T21889 1426-1427 . denotes .
T21890 1427-1502 sentence denotes MMU2 speed congenic strains were maintained through brother-sister mating.
T21891 1428-1432 NN denotes MMU2
T21892 1448-1455 NNS denotes strains
T21893 1433-1438 NN denotes speed
T21894 1439-1447 JJ denotes congenic
T21895 1461-1471 VBN denotes maintained
T21896 1456-1460 VBD denotes were
T21897 1472-1479 IN denotes through
T21898 1480-1487 NN denotes brother
T21899 1488-1494 NN denotes sister
T21900 1487-1488 HYPH denotes -
T21901 1495-1501 NN denotes mating
T21902 1501-1502 . denotes .
T21903 1502-1667 sentence denotes Once each congenic was stabilized, 20 additional microsatellite markers were used to refine the position of each congenic recombinant end point (Additional File 2).
T21904 1503-1507 RB denotes Once
T21905 1526-1536 VBN denotes stabilized
T21906 1508-1512 DT denotes each
T21907 1513-1521 JJ denotes congenic
T21908 1522-1525 VBD denotes was
T21909 1580-1584 VBN denotes used
T21910 1536-1538 , denotes ,
T21911 1538-1540 CD denotes 20
T21912 1567-1574 NNS denotes markers
T21913 1541-1551 JJ denotes additional
T21914 1552-1566 NN denotes microsatellite
T21915 1575-1579 VBD denotes were
T21916 1585-1587 TO denotes to
T21917 1588-1594 VB denotes refine
T21918 1595-1598 DT denotes the
T21919 1599-1607 NN denotes position
T21920 1608-1610 IN denotes of
T21921 1611-1615 DT denotes each
T21922 1641-1646 NN denotes point
T21923 1616-1624 JJ denotes congenic
T21924 1625-1636 JJ denotes recombinant
T21925 1637-1640 NN denotes end
T21926 1647-1648 -LRB- denotes (
T21927 1659-1663 NN denotes File
T21928 1648-1658 JJ denotes Additional
T21929 1664-1665 CD denotes 2
T21930 1665-1666 -RRB- denotes )
T21931 1666-1667 . denotes .
R6585 T21608 T21607 prep of,Development
R6586 T21609 T21610 nmod B6.CAST,MMU2
R6587 T21610 T21613 nmod MMU2,strains
R6588 T21611 T21609 cc and,B6.CAST
R6589 T21612 T21609 conj HG.CAST,B6.CAST
R6590 T21613 T21608 pobj strains,of
R6591 T21614 T21615 npadvmod speed,congenic
R6592 T21615 T21613 amod congenic,strains
R6593 T21617 T21618 det All,strains
R6594 T21618 T21621 nsubjpass strains,developed
R6595 T21619 T21620 npadvmod speed,congenic
R6596 T21620 T21618 amod congenic,strains
R6597 T21622 T21621 auxpass were,developed
R6598 T21623 T21621 advcl starting,developed
R6599 T21624 T21623 prep with,starting
R6600 T21625 T21626 det an,cross
R6601 T21626 T21624 pobj cross,with
R6602 T21627 T21626 amod initial,cross
R6603 T21628 T21626 prep between,cross
R6604 T21629 T21630 det a,male
R6605 T21630 T21628 pobj male,between
R6606 T21631 T21630 compound CAST,male
R6607 T21632 T21630 cc and,male
R6608 T21633 T21634 compound HG,females
R6609 T21634 T21630 conj females,male
R6610 T21635 T21636 punct (,Figure
R6611 T21636 T21623 parataxis Figure,starting
R6612 T21637 T21636 nummod 1,Figure
R6613 T21638 T21636 punct ),Figure
R6614 T21639 T21640 punct [,6
R6615 T21640 T21621 parataxis 6,developed
R6616 T21641 T21640 nummod 5,6
R6617 T21642 T21640 punct ",",6
R6618 T21643 T21640 punct ],6
R6619 T21644 T21621 punct .,developed
R6620 T21646 T21647 amod Male,mice
R6621 T21647 T21649 nsubjpass mice,backcrossed
R6622 T21648 T21647 compound F1,mice
R6623 T21650 T21649 auxpass were,backcrossed
R6624 T21651 T21649 advmod then,backcrossed
R6625 T21652 T21649 prep to,backcrossed
R6626 T21653 T21654 compound HG,females
R6627 T21654 T21652 pobj females,to
R6628 T21655 T21649 punct .,backcrossed
R6629 T21657 T21658 det All,males
R6631 T21659 T21658 nmod agouti,males
R6632 T21660 T21661 punct (,located
R6633 T21661 T21658 parataxis located,males
R6634 T21662 T21663 det the,locus
R6635 T21663 T21661 nsubjpass locus,located
R6636 T21664 T21663 amod dominant,locus
R6637 T21665 T21666 amod nonagouti,a
R6638 T21666 T21663 amod a,locus
R6639 T21667 T21666 punct (,a
R6640 T21668 T21663 punct ),locus
R6641 T21669 T21661 auxpass is,located
R6642 T21670 T21661 prep at,located
R6643 T21671 T21672 nummod 154.8,Mbp
R6644 T21672 T21670 pobj Mbp,at
R6645 T21673 T21661 prep on,located
R6646 T21674 T21673 pobj MMU2,on
R6647 T21675 T21661 punct ),located
R6648 T21676 T21658 compound N2,males
R6649 T21678 T21677 auxpass were,genotyped
R6650 T21679 T21677 prep for,genotyped
R6651 T21680 T21681 nummod 79,markers
R6652 T21681 T21679 pobj markers,for
R6653 T21682 T21681 compound microsatellite,markers
R6654 T21683 T21684 punct (,File
R6655 T21684 T21677 parataxis File,genotyped
R6656 T21685 T21684 amod Additional,File
R6657 T21686 T21684 nummod 1,File
R6658 T21687 T21684 punct ),File
R6659 T21688 T21677 punct .,genotyped
R6660 T21690 T21691 det These,markers
R6661 T21691 T21692 nsubjpass markers,spaced
R6662 T21693 T21692 auxpass were,spaced
R6663 T21694 T21692 advmod evenly,spaced
R6664 T21695 T21692 prep across,spaced
R6665 T21696 T21697 det the,genome
R6666 T21697 T21695 pobj genome,across
R6667 T21698 T21692 punct ", ",spaced
R6668 T21699 T21700 advmod except,in
R6669 T21700 T21692 prep in,spaced
R6670 T21701 T21700 pobj regions,in
R6671 T21702 T21703 advmod previously,identified
R6672 T21703 T21701 acl identified,regions
R6673 T21704 T21703 prep as,identified
R6674 T21705 T21704 pcomp harboring,as
R6675 T21706 T21705 dobj QTL,harboring
R6676 T21707 T21708 punct [,1
R6677 T21708 T21705 parataxis 1,harboring
R6678 T21709 T21708 punct ],1
R6679 T21710 T21701 punct ", ",regions
R6680 T21711 T21712 dep which,screened
R6681 T21712 T21701 relcl screened,regions
R6682 T21713 T21712 auxpass were,screened
R6683 T21714 T21715 advmod more,densely
R6684 T21715 T21712 advmod densely,screened
R6685 T21716 T21692 punct .,spaced
R6686 T21718 T21719 det The,male
R6687 T21719 T21725 nsubjpass male,selected
R6688 T21720 T21719 punct """",male
R6689 T21721 T21719 amod best,male
R6690 T21722 T21719 punct """",male
R6691 T21723 T21724 compound N2,agouti
R6692 T21724 T21719 compound agouti,male
R6693 T21726 T21719 prep with,male
R6694 T21727 T21728 det the,level
R6695 T21728 T21726 pobj level,with
R6696 T21729 T21728 amod lowest,level
R6697 T21730 T21728 prep of,level
R6698 T21731 T21732 npadvmod genome,wide
R6699 T21732 T21734 amod wide,heterozygosity
R6700 T21733 T21732 punct -,wide
R6701 T21734 T21730 pobj heterozygosity,of
R6702 T21735 T21734 amod unwanted,heterozygosity
R6703 T21736 T21737 mark while,maintaining
R6704 T21737 T21725 advcl maintaining,selected
R6705 T21738 T21739 compound CAST,alleles
R6706 T21739 T21737 dobj alleles,maintaining
R6707 T21740 T21739 prep for,alleles
R6708 T21741 T21742 det all,markers
R6709 T21742 T21740 pobj markers,for
R6710 T21743 T21742 compound MMU2,markers
R6711 T21744 T21725 auxpass was,selected
R6712 T21745 T21725 prep for,selected
R6713 T21746 T21745 pobj breeding,for
R6714 T21747 T21725 punct .,selected
R6715 T21749 T21750 det This,scheme
R6716 T21750 T21752 nsubjpass scheme,used
R6717 T21751 T21750 compound selection,scheme
R6718 T21753 T21752 auxpass was,used
R6719 T21754 T21752 prep at,used
R6720 T21755 T21756 det each,generation
R6721 T21756 T21754 pobj generation,at
R6722 T21757 T21758 mark until,identified
R6723 T21758 T21752 advcl identified,used
R6724 T21759 T21760 det a,male
R6725 T21760 T21758 nsubjpass male,identified
R6726 T21761 T21760 compound N4,male
R6727 T21762 T21758 auxpass was,identified
R6728 T21763 T21758 prep as,identified
R6729 T21764 T21765 amod homozygous,HG
R6730 T21765 T21763 pobj HG,as
R6731 T21766 T21765 prep for,HG
R6732 T21767 T21768 det all,markers
R6733 T21768 T21766 pobj markers,for
R6734 T21769 T21768 acl typed,markers
R6735 T21770 T21769 prep outside,typed
R6736 T21771 T21770 pobj MMU2,outside
R6737 T21772 T21752 punct .,used
R6738 T21774 T21775 prep After,identified
R6739 T21776 T21777 det an,backcross
R6740 T21777 T21774 pobj backcross,After
R6741 T21778 T21777 amod additional,backcross
R6742 T21779 T21777 prep to,backcross
R6743 T21780 T21781 compound HG,females
R6744 T21781 T21779 pobj females,to
R6745 T21782 T21775 punct ", ",identified
R6746 T21783 T21784 amod recombinant,males
R6747 T21784 T21775 nsubjpass males,identified
R6748 T21785 T21775 auxpass were,identified
R6749 T21786 T21775 advcl providing,identified
R6750 T21787 T21788 det the,foundation
R6751 T21788 T21786 dobj foundation,providing
R6752 T21789 T21788 prep for,foundation
R6753 T21790 T21791 det the,regions
R6754 T21791 T21789 pobj regions,for
R6755 T21792 T21791 nummod four,regions
R6756 T21793 T21791 amod overlapping,regions
R6757 T21794 T21791 compound donor,regions
R6758 T21795 T21775 punct .,identified
R6759 T21797 T21798 amod Selected,males
R6760 T21798 T21800 nsubjpass males,backcrossed
R6761 T21799 T21798 amod recombinant,males
R6762 T21801 T21800 auxpass were,backcrossed
R6763 T21802 T21800 advmod then,backcrossed
R6764 T21803 T21800 prep to,backcrossed
R6765 T21804 T21805 preconj both,B6
R6766 T21805 T21806 nmod B6,females
R6767 T21806 T21803 pobj females,to
R6768 T21807 T21805 cc and,B6
R6769 T21808 T21805 conj HG,B6
R6770 T21809 T21810 aux to,create
R6771 T21810 T21800 advcl create,backcrossed
R6772 T21811 T21810 dobj strains,create
R6773 T21812 T21811 punct ", ",strains
R6774 T21813 T21814 dep which,were
R6775 T21814 T21811 relcl were,strains
R6776 T21815 T21816 npadvmod B6,congenic
R6777 T21816 T21814 acomp congenic,were
R6778 T21817 T21818 punct (,+
R6779 T21818 T21815 punct +,B6
R6780 T21819 T21818 punct +,+
R6781 T21820 T21818 punct /,+
R6782 T21821 T21818 punct ),+
R6783 T21822 T21815 cc or,B6
R6784 T21823 T21815 conj HG,B6
R6785 T21824 T21825 punct (,hg
R6786 T21825 T21823 parataxis hg,HG
R6787 T21826 T21825 compound hg,hg
R6788 T21827 T21825 punct /,hg
R6789 T21828 T21825 punct ),hg
R6790 T21829 T21815 cc and,B6
R6791 T21830 T21815 conj heterozygous,B6
R6792 T21831 T21800 punct .,backcrossed
R6793 T21833 T21834 det These,mice
R6794 T21834 T21835 nsubjpass mice,intermated
R6795 T21836 T21835 auxpass were,intermated
R6796 T21837 T21838 aux to,produce
R6797 T21838 T21835 advcl produce,intermated
R6798 T21839 T21840 amod homozygous,founders
R6799 T21840 T21838 dobj founders,produce
R6800 T21841 T21838 prep for,produce
R6801 T21842 T21843 det each,strain
R6802 T21843 T21841 pobj strain,for
R6803 T21844 T21835 punct .,intermated
R6804 T21846 T21847 det This,scheme
R6805 T21847 T21850 nsubj scheme,created
R6806 T21848 T21847 amod novel,scheme
R6807 T21849 T21847 amod breeding,scheme
R6808 T21851 T21852 nummod four,congenics
R6809 T21852 T21850 dobj congenics,created
R6810 T21853 T21852 amod identical,congenics
R6811 T21854 T21852 compound founder,congenics
R6812 T21855 T21852 prep on,congenics
R6813 T21856 T21857 nummod two,backgrounds
R6814 T21857 T21855 pobj backgrounds,on
R6815 T21858 T21857 appos B6,backgrounds
R6816 T21859 T21860 punct (,+
R6817 T21860 T21858 punct +,B6
R6818 T21861 T21860 punct +,+
R6819 T21862 T21860 punct /,+
R6820 T21863 T21860 punct ),+
R6821 T21864 T21858 cc and,B6
R6822 T21865 T21858 conj HG,B6
R6823 T21866 T21867 punct (,hg
R6824 T21867 T21865 parataxis hg,HG
R6825 T21868 T21867 compound hg,hg
R6826 T21869 T21867 punct /,hg
R6827 T21870 T21867 punct ),hg
R6828 T21871 T21857 punct ", ",backgrounds
R6829 T21872 T21873 dep which,formed
R6830 T21873 T21857 relcl formed,backgrounds
R6831 T21874 T21875 det the,basis
R6832 T21875 T21873 dobj basis,formed
R6833 T21876 T21875 prep for,basis
R6834 T21877 T21878 poss our,examination
R6835 T21878 T21876 pobj examination,for
R6836 T21879 T21878 prep of,examination
R6837 T21880 T21879 pobj interactions,of
R6838 T21881 T21880 acl caused,interactions
R6839 T21882 T21881 agent by,caused
R6840 T21883 T21884 det the,presence
R6841 T21884 T21882 pobj presence,by
R6842 T21885 T21884 prep of,presence
R6843 T21886 T21887 det the,deletion
R6844 T21887 T21885 pobj deletion,of
R6845 T21888 T21887 compound hg,deletion
R6846 T21889 T21850 punct .,created
R6847 T21891 T21892 nmod MMU2,strains
R6848 T21892 T21895 nsubjpass strains,maintained
R6849 T21893 T21894 npadvmod speed,congenic
R6850 T21894 T21892 amod congenic,strains
R6851 T21896 T21895 auxpass were,maintained
R6852 T21897 T21895 prep through,maintained
R6853 T21898 T21899 compound brother,sister
R6854 T21899 T21901 compound sister,mating
R6855 T21900 T21899 punct -,sister
R6856 T21901 T21897 pobj mating,through
R6857 T21902 T21895 punct .,maintained
R6858 T21904 T21905 advmod Once,stabilized
R6859 T21905 T21909 advcl stabilized,used
R6860 T21906 T21907 det each,congenic
R6861 T21907 T21905 nsubjpass congenic,stabilized
R6862 T21908 T21905 auxpass was,stabilized
R6863 T21910 T21909 punct ", ",used
R6864 T21911 T21912 nummod 20,markers
R6865 T21912 T21909 nsubjpass markers,used
R6866 T21913 T21912 amod additional,markers
R6867 T21914 T21912 compound microsatellite,markers
R6868 T21915 T21909 auxpass were,used
R6869 T21916 T21917 aux to,refine
R6870 T21917 T21909 advcl refine,used
R6871 T21918 T21919 det the,position
R6872 T21919 T21917 dobj position,refine
R6873 T21920 T21919 prep of,position
R6874 T21921 T21922 det each,point
R6875 T21922 T21920 pobj point,of
R6876 T21923 T21922 amod congenic,point
R6877 T21924 T21922 amod recombinant,point
R6878 T21925 T21922 compound end,point
R6879 T21926 T21927 punct (,File
R6880 T21927 T21909 parataxis File,used
R6881 T21928 T21927 amod Additional,File
R6882 T21929 T21927 nummod 2,File
R6883 T21930 T21927 punct ),File
R6884 T21931 T21909 punct .,used
R6630 T21658 T21677 nsubjpass males,genotyped

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
T21570 151-155 PATO_UBERON_EXT:male_or_bearer_of_maleness denotes male
T21571 163-170 PATO_UBERON_EXT:female_or_bearer_of_femaleness denotes females
T21572 189-193 PATO_UBERON_EXT:male_or_bearer_of_maleness denotes Male
T21573 197-201 NCBITaxon:10088 denotes mice
T21574 230-237 PATO_UBERON_EXT:female_or_bearer_of_femaleness denotes females
T21575 305-307 SO_EXT:0000028 denotes bp
T21576 320-325 PATO_UBERON_EXT:male_or_bearer_of_maleness denotes males
T21577 348-362 SO_EXT:microsatellite_unit_or_region denotes microsatellite
T21578 363-370 CHEBI_SO_EXT:molecular_indicator_or_label_or_marker_or_tag denotes markers
T21579 398-405 CHEBI_SO_EXT:molecular_indicator_or_label_or_marker_or_tag denotes markers
T21580 436-442 SO_EXT:0001026 denotes genome
T21581 497-500 SO_EXT:0000771 denotes QTL
T21582 561-565 PATO_UBERON_EXT:male_or_bearer_of_maleness denotes male
T21583 591-597 SO_EXT:0001026 denotes genome
T21584 650-657 SO_EXT:0001023 denotes alleles
T21585 671-678 CHEBI_SO_EXT:molecular_indicator_or_label_or_marker_or_tag denotes markers
T21586 696-704 GO_EXT:breeding denotes breeding
T21587 767-771 PATO_UBERON_EXT:male_or_bearer_of_maleness denotes male
T21588 812-819 CHEBI_SO_EXT:molecular_indicator_or_label_or_marker_or_tag denotes markers
T21589 876-883 PATO_UBERON_EXT:female_or_bearer_of_femaleness denotes females
T21590 885-896 GO_SO_EXT:sequence_rearrangement_process denotes recombinant
T21591 897-902 PATO_UBERON_EXT:male_or_bearer_of_maleness denotes males
T21592 993-1004 GO_SO_EXT:sequence_rearrangement_process denotes recombinant
T21593 1005-1010 PATO_UBERON_EXT:male_or_bearer_of_maleness denotes males
T21594 1051-1058 PATO_UBERON_EXT:female_or_bearer_of_femaleness denotes females
T21595 1093-1094 SO_EXT:normal_or_wild_type_or_present denotes +
T21596 1095-1096 SO_EXT:normal_or_wild_type_or_present denotes +
T21597 1145-1149 NCBITaxon:10088 denotes mice
T21598 1160-1165 GO:0007618 denotes mated
T21599 1225-1233 GO_EXT:breeding denotes breeding
T21600 1305-1306 SO_EXT:normal_or_wild_type_or_present denotes +
T21601 1307-1308 SO_EXT:normal_or_wild_type_or_present denotes +
T21602 1418-1426 SO_EXT:sequence_deletion_entity_or_process denotes deletion
T21603 1495-1501 GO:0007618 denotes mating
T21604 1552-1566 SO_EXT:microsatellite_unit_or_region denotes microsatellite
T21605 1567-1574 CHEBI_SO_EXT:molecular_indicator_or_label_or_marker_or_tag denotes markers
T21606 1625-1636 GO_SO_EXT:sequence_rearrangement_process denotes recombinant

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
T21561 197-201 NCBITaxon:10088 denotes mice
T21562 305-307 SO:0000028 denotes bp
T21563 436-442 SO:0001026 denotes genome
T21564 497-500 SO:0000771 denotes QTL
T21565 591-597 SO:0001026 denotes genome
T21566 650-657 SO:0001023 denotes alleles
T21567 1145-1149 NCBITaxon:10088 denotes mice
T21568 1160-1165 GO:0007618 denotes mated
T21569 1495-1501 GO:0007618 denotes mating