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PMC:1617083 / 27914-29387 JSONTXT 4 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue
T18534 0-2 IN denotes In
T18536 3-7 DT denotes this
T18537 8-13 NN denotes study
T18538 13-15 , denotes ,
T18539 15-25 JJ denotes thrombotic
T18540 26-30 NN denotes risk
T18541 31-34 VBD denotes was
T18542 35-49 RB denotes systematically
T18535 50-58 VBN denotes assessed
T18543 59-61 IN denotes in
T18544 62-65 CD denotes two
T18546 66-72 JJ denotes inbred
T18545 73-80 NNS denotes strains
T18547 81-83 IN denotes of
T18548 84-88 NNS denotes mice
T18549 89-93 WDT denotes that
T18550 94-98 VBP denotes have
T18551 99-105 VBN denotes marked
T18552 106-117 NNS denotes differences
T18553 118-120 IN denotes in
T18554 121-135 NN denotes susceptibility
T18555 136-138 IN denotes to
T18556 139-143 NN denotes diet
T18558 143-144 HYPH denotes -
T18557 144-151 VBN denotes induced
T18559 152-159 NN denotes obesity
T18560 159-161 , denotes ,
T18561 161-165 NN denotes diet
T18563 165-166 HYPH denotes -
T18562 166-173 VBN denotes induced
T18564 174-189 NN denotes atherosclerosis
T18565 189-191 , denotes ,
T18566 191-194 CC denotes and
T18567 195-203 NN denotes ligation
T18569 203-204 HYPH denotes -
T18568 204-211 VBN denotes induced
T18571 212-222 JJ denotes neointimal
T18570 223-234 NN denotes hyperplasia
T18572 235-238 CC denotes and
T18573 239-245 NN denotes vessel
T18574 246-256 NN denotes remodeling
T18575 256-257 . denotes .
T18576 257-379 sentence denotes Arterial occlusion time, tail bleeding and rebleeding time were evaluated as potential predictors of thrombotic response.
T18577 258-266 JJ denotes Arterial
T18578 267-276 NN denotes occlusion
T18579 277-281 NN denotes time
T18581 281-283 , denotes ,
T18582 283-287 NN denotes tail
T18583 288-296 NN denotes bleeding
T18585 297-300 CC denotes and
T18586 301-311 NN denotes rebleeding
T18584 312-316 NN denotes time
T18587 317-321 VBD denotes were
T18580 322-331 VBN denotes evaluated
T18588 332-334 IN denotes as
T18589 335-344 JJ denotes potential
T18590 345-355 NNS denotes predictors
T18591 356-358 IN denotes of
T18592 359-369 JJ denotes thrombotic
T18593 370-378 NN denotes response
T18594 378-379 . denotes .
T18595 379-591 sentence denotes Assessments of the two inbred strains were compared to values from gene targeted mice of the Plg network with altered fibrinolytic responses, as well as in leptin deficient mice with a reduced platelet function.
T18596 380-391 NNS denotes Assessments
T18598 392-394 IN denotes of
T18599 395-398 DT denotes the
T18601 399-402 CD denotes two
T18602 403-409 JJ denotes inbred
T18600 410-417 NNS denotes strains
T18603 418-422 VBD denotes were
T18597 423-431 VBN denotes compared
T18604 432-434 IN denotes to
T18605 435-441 NNS denotes values
T18606 442-446 IN denotes from
T18607 447-451 NN denotes gene
T18608 452-460 VBN denotes targeted
T18609 461-465 NNS denotes mice
T18610 466-468 IN denotes of
T18611 469-472 DT denotes the
T18613 473-476 NN denotes Plg
T18612 477-484 NN denotes network
T18614 485-489 IN denotes with
T18615 490-497 VBN denotes altered
T18617 498-510 JJ denotes fibrinolytic
T18616 511-520 NNS denotes responses
T18618 520-522 , denotes ,
T18619 522-524 RB denotes as
T18621 525-529 RB denotes well
T18620 530-532 IN denotes as
T18622 533-535 IN denotes in
T18623 536-542 NN denotes leptin
T18624 543-552 JJ denotes deficient
T18625 553-557 NNS denotes mice
T18626 558-562 IN denotes with
T18627 563-564 DT denotes a
T18629 565-572 VBN denotes reduced
T18630 573-581 NN denotes platelet
T18628 582-590 NN denotes function
T18631 590-591 . denotes .
T18632 591-788 sentence denotes Marked differences were found in the thrombotic response among the two inbred strains, B6 and A/J, and the observed differences were not correlated with change in coagulation or platelet function.
T18633 592-598 JJ denotes Marked
T18634 599-610 NNS denotes differences
T18636 611-615 VBD denotes were
T18635 616-621 VBN denotes found
T18637 622-624 IN denotes in
T18638 625-628 DT denotes the
T18640 629-639 JJ denotes thrombotic
T18639 640-648 NN denotes response
T18641 649-654 IN denotes among
T18642 655-658 DT denotes the
T18644 659-662 CD denotes two
T18645 663-669 JJ denotes inbred
T18643 670-677 NNS denotes strains
T18646 677-679 , denotes ,
T18647 679-681 NN denotes B6
T18648 682-685 CC denotes and
T18649 686-687 NN denotes A
T18651 687-688 HYPH denotes /
T18650 688-689 NN denotes J
T18652 689-691 , denotes ,
T18653 691-694 CC denotes and
T18654 695-698 DT denotes the
T18656 699-707 VBN denotes observed
T18655 708-719 NNS denotes differences
T18658 720-724 VBD denotes were
T18659 725-728 RB denotes not
T18657 729-739 VBN denotes correlated
T18660 740-744 IN denotes with
T18661 745-751 NN denotes change
T18662 752-754 IN denotes in
T18663 755-766 NN denotes coagulation
T18664 767-769 CC denotes or
T18665 770-778 NN denotes platelet
T18666 779-787 NN denotes function
T18667 787-788 . denotes .
T18668 788-924 sentence denotes Screening the CSS identified three chromosomes that harbored genes which contributed to the A/J phenotype of increased rebleeding time.
T18669 789-798 VBG denotes Screening
T18671 799-802 DT denotes the
T18672 803-806 NN denotes CSS
T18670 807-817 VBD denotes identified
T18673 818-823 CD denotes three
T18674 824-835 NNS denotes chromosomes
T18675 836-840 WDT denotes that
T18676 841-849 VBD denotes harbored
T18677 850-855 NNS denotes genes
T18678 856-861 WDT denotes which
T18679 862-873 VBD denotes contributed
T18680 874-876 IN denotes to
T18681 877-880 DT denotes the
T18683 881-882 NN denotes A
T18685 882-883 HYPH denotes /
T18684 883-884 NN denotes J
T18682 885-894 NN denotes phenotype
T18686 895-897 IN denotes of
T18687 898-907 VBN denotes increased
T18689 908-918 NN denotes rebleeding
T18688 919-923 NN denotes time
T18690 923-924 . denotes .
T18691 924-1091 sentence denotes Mice homosomic for these chromosomes or doubly heterosomic for two of the chromosomes, 5 and 17, were required to express the A/J phenotype, elevated rebleeding time.
T18692 925-929 NNS denotes Mice
T18694 930-939 JJ denotes homosomic
T18695 940-943 IN denotes for
T18696 944-949 DT denotes these
T18697 950-961 NNS denotes chromosomes
T18698 962-964 CC denotes or
T18699 965-971 RB denotes doubly
T18700 972-983 JJ denotes heterosomic
T18701 984-987 IN denotes for
T18702 988-991 CD denotes two
T18703 992-994 IN denotes of
T18704 995-998 DT denotes the
T18705 999-1010 NNS denotes chromosomes
T18706 1010-1012 , denotes ,
T18707 1012-1013 CD denotes 5
T18708 1014-1017 CC denotes and
T18709 1018-1020 CD denotes 17
T18710 1020-1022 , denotes ,
T18711 1022-1026 VBD denotes were
T18693 1027-1035 VBN denotes required
T18712 1036-1038 TO denotes to
T18713 1039-1046 VB denotes express
T18714 1047-1050 DT denotes the
T18716 1051-1052 NN denotes A
T18718 1052-1053 HYPH denotes /
T18717 1053-1054 NN denotes J
T18715 1055-1064 NN denotes phenotype
T18719 1064-1066 , denotes ,
T18720 1066-1074 VBN denotes elevated
T18722 1075-1085 NN denotes rebleeding
T18721 1086-1090 NN denotes time
T18723 1090-1091 . denotes .
T18724 1091-1236 sentence denotes PAI-1 antigen and activity were decreased in both CSS-5 and CSS-17 and the heterosomic mice, CSS-5F1 and CSS-17F1, but not in the CSS-11 strain.
T18725 1092-1095 NN denotes PAI
T18727 1095-1096 HYPH denotes -
T18728 1096-1097 CD denotes 1
T18729 1098-1105 NN denotes antigen
T18730 1106-1109 CC denotes and
T18731 1110-1118 NN denotes activity
T18732 1119-1123 VBD denotes were
T18726 1124-1133 VBN denotes decreased
T18733 1134-1136 IN denotes in
T18734 1137-1141 CC denotes both
T18735 1142-1145 NN denotes CSS
T18736 1145-1146 HYPH denotes -
T18737 1146-1147 CD denotes 5
T18738 1148-1151 CC denotes and
T18739 1152-1155 NN denotes CSS
T18740 1155-1156 HYPH denotes -
T18741 1156-1158 CD denotes 17
T18742 1159-1162 CC denotes and
T18743 1163-1166 DT denotes the
T18745 1167-1178 JJ denotes heterosomic
T18744 1179-1183 NNS denotes mice
T18746 1183-1185 , denotes ,
T18747 1185-1188 NN denotes CSS
T18749 1188-1189 HYPH denotes -
T18748 1189-1192 NN denotes 5F1
T18750 1193-1196 CC denotes and
T18751 1197-1200 NN denotes CSS
T18753 1200-1201 HYPH denotes -
T18752 1201-1205 NN denotes 17F1
T18754 1205-1207 , denotes ,
T18755 1207-1210 CC denotes but
T18756 1211-1214 RB denotes not
T18757 1215-1217 IN denotes in
T18758 1218-1221 DT denotes the
T18760 1222-1225 NN denotes CSS
T18761 1225-1226 HYPH denotes -
T18762 1226-1228 CD denotes 11
T18759 1229-1235 NN denotes strain
T18763 1235-1236 . denotes .
T18764 1236-1317 sentence denotes Values were restored in the doubly heterosomic for two of chromosomes, 5 and 17.
T18765 1237-1243 NNS denotes Values
T18767 1244-1248 VBD denotes were
T18766 1249-1257 VBN denotes restored
T18768 1258-1260 IN denotes in
T18769 1261-1264 DT denotes the
T18771 1265-1271 RB denotes doubly
T18770 1272-1283 JJ denotes heterosomic
T18772 1284-1287 IN denotes for
T18773 1288-1291 CD denotes two
T18774 1292-1294 IN denotes of
T18775 1295-1306 NNS denotes chromosomes
T18776 1306-1308 , denotes ,
T18777 1308-1309 CD denotes 5
T18778 1310-1313 CC denotes and
T18779 1314-1316 CD denotes 17
T18780 1316-1317 . denotes .
T18781 1317-1473 sentence denotes Arterial occlusion time was similar to B6 in the CSS-5 and CSS-17 homozygous strains, but increased in doubly heterosomic for two of chromosomes, 5 and 17.
T18782 1318-1326 JJ denotes Arterial
T18783 1327-1336 NN denotes occlusion
T18784 1337-1341 NN denotes time
T18785 1342-1345 VBD denotes was
T18786 1346-1353 JJ denotes similar
T18787 1354-1356 IN denotes to
T18788 1357-1359 NN denotes B6
T18789 1360-1362 IN denotes in
T18790 1363-1366 DT denotes the
T18792 1367-1370 NN denotes CSS
T18793 1370-1371 HYPH denotes -
T18794 1371-1372 CD denotes 5
T18795 1373-1376 CC denotes and
T18796 1377-1380 NN denotes CSS
T18797 1380-1381 HYPH denotes -
T18798 1381-1383 CD denotes 17
T18799 1384-1394 JJ denotes homozygous
T18791 1395-1402 NNS denotes strains
T18800 1402-1404 , denotes ,
T18801 1404-1407 CC denotes but
T18802 1408-1417 VBD denotes increased
T18803 1418-1420 IN denotes in
T18804 1421-1427 RB denotes doubly
T18805 1428-1439 JJ denotes heterosomic
T18806 1440-1443 IN denotes for
T18807 1444-1447 CD denotes two
T18808 1448-1450 IN denotes of
T18809 1451-1462 NNS denotes chromosomes
T18810 1462-1464 , denotes ,
T18811 1464-1465 CD denotes 5
T18812 1466-1469 CC denotes and
T18813 1470-1472 CD denotes 17
T18814 1472-1473 . denotes .
R4737 T18534 T18535 prep In,assessed
R4738 T18536 T18537 det this,study
R4739 T18537 T18534 pobj study,In
R4740 T18538 T18535 punct ", ",assessed
R4741 T18539 T18540 amod thrombotic,risk
R4742 T18540 T18535 nsubjpass risk,assessed
R4743 T18541 T18535 auxpass was,assessed
R4744 T18542 T18535 advmod systematically,assessed
R4745 T18543 T18535 prep in,assessed
R4746 T18544 T18545 nummod two,strains
R4747 T18545 T18543 pobj strains,in
R4748 T18546 T18545 amod inbred,strains
R4749 T18547 T18545 prep of,strains
R4750 T18548 T18547 pobj mice,of
R4751 T18549 T18550 dep that,have
R4752 T18550 T18545 relcl have,strains
R4753 T18551 T18552 amod marked,differences
R4754 T18552 T18550 dobj differences,have
R4755 T18553 T18552 prep in,differences
R4756 T18554 T18553 pobj susceptibility,in
R4757 T18555 T18554 prep to,susceptibility
R4758 T18556 T18557 npadvmod diet,induced
R4759 T18557 T18559 amod induced,obesity
R4760 T18558 T18557 punct -,induced
R4761 T18559 T18555 pobj obesity,to
R4762 T18560 T18559 punct ", ",obesity
R4763 T18561 T18562 npadvmod diet,induced
R4764 T18562 T18564 amod induced,atherosclerosis
R4765 T18563 T18562 punct -,induced
R4766 T18564 T18559 conj atherosclerosis,obesity
R4767 T18565 T18564 punct ", ",atherosclerosis
R4768 T18566 T18564 cc and,atherosclerosis
R4769 T18567 T18568 npadvmod ligation,induced
R4770 T18568 T18570 amod induced,hyperplasia
R4771 T18569 T18568 punct -,induced
R4772 T18570 T18564 conj hyperplasia,atherosclerosis
R4773 T18571 T18570 amod neointimal,hyperplasia
R4774 T18572 T18570 cc and,hyperplasia
R4775 T18573 T18574 compound vessel,remodeling
R4776 T18574 T18570 conj remodeling,hyperplasia
R4777 T18575 T18535 punct .,assessed
R4778 T18577 T18578 amod Arterial,occlusion
R4779 T18578 T18579 compound occlusion,time
R4780 T18579 T18580 nsubjpass time,evaluated
R4781 T18581 T18579 punct ", ",time
R4782 T18582 T18583 nmod tail,bleeding
R4783 T18583 T18584 nmod bleeding,time
R4784 T18584 T18579 appos time,time
R4785 T18585 T18583 cc and,bleeding
R4786 T18586 T18583 conj rebleeding,bleeding
R4787 T18587 T18580 auxpass were,evaluated
R4788 T18588 T18580 prep as,evaluated
R4789 T18589 T18590 amod potential,predictors
R4790 T18590 T18588 pobj predictors,as
R4791 T18591 T18590 prep of,predictors
R4792 T18592 T18593 amod thrombotic,response
R4793 T18593 T18591 pobj response,of
R4794 T18594 T18580 punct .,evaluated
R4795 T18596 T18597 nsubjpass Assessments,compared
R4796 T18598 T18596 prep of,Assessments
R4797 T18599 T18600 det the,strains
R4798 T18600 T18598 pobj strains,of
R4799 T18601 T18600 nummod two,strains
R4800 T18602 T18600 amod inbred,strains
R4801 T18603 T18597 auxpass were,compared
R4802 T18604 T18597 prep to,compared
R4803 T18605 T18604 pobj values,to
R4804 T18606 T18605 prep from,values
R4805 T18607 T18608 npadvmod gene,targeted
R4806 T18608 T18609 amod targeted,mice
R4807 T18609 T18606 pobj mice,from
R4808 T18610 T18609 prep of,mice
R4809 T18611 T18612 det the,network
R4810 T18612 T18610 pobj network,of
R4811 T18613 T18612 compound Plg,network
R4812 T18614 T18609 prep with,mice
R4813 T18615 T18616 amod altered,responses
R4814 T18616 T18614 pobj responses,with
R4815 T18617 T18616 amod fibrinolytic,responses
R4816 T18618 T18606 punct ", ",from
R4817 T18619 T18620 advmod as,as
R4818 T18620 T18606 cc as,from
R4819 T18621 T18620 advmod well,as
R4820 T18622 T18606 conj in,from
R4821 T18623 T18624 npadvmod leptin,deficient
R4822 T18624 T18625 amod deficient,mice
R4823 T18625 T18622 pobj mice,in
R4824 T18626 T18625 prep with,mice
R4825 T18627 T18628 det a,function
R4826 T18628 T18626 pobj function,with
R4827 T18629 T18628 amod reduced,function
R4828 T18630 T18628 compound platelet,function
R4829 T18631 T18597 punct .,compared
R4830 T18633 T18634 amod Marked,differences
R4831 T18634 T18635 nsubjpass differences,found
R4832 T18636 T18635 auxpass were,found
R4833 T18637 T18635 prep in,found
R4834 T18638 T18639 det the,response
R4835 T18639 T18637 pobj response,in
R4836 T18640 T18639 amod thrombotic,response
R4837 T18641 T18635 prep among,found
R4838 T18642 T18643 det the,strains
R4839 T18643 T18641 pobj strains,among
R4840 T18644 T18643 nummod two,strains
R4841 T18645 T18643 amod inbred,strains
R4842 T18646 T18643 punct ", ",strains
R4843 T18647 T18643 appos B6,strains
R4844 T18648 T18647 cc and,B6
R4845 T18649 T18650 compound A,J
R4846 T18650 T18647 conj J,B6
R4847 T18651 T18650 punct /,J
R4848 T18652 T18635 punct ", ",found
R4849 T18653 T18635 cc and,found
R4850 T18654 T18655 det the,differences
R4851 T18655 T18657 nsubjpass differences,correlated
R4852 T18656 T18655 amod observed,differences
R4853 T18657 T18635 conj correlated,found
R4854 T18658 T18657 auxpass were,correlated
R4855 T18659 T18657 neg not,correlated
R4856 T18660 T18657 prep with,correlated
R4857 T18661 T18660 pobj change,with
R4858 T18662 T18661 prep in,change
R4859 T18663 T18662 pobj coagulation,in
R4860 T18664 T18663 cc or,coagulation
R4861 T18665 T18666 compound platelet,function
R4862 T18666 T18663 conj function,coagulation
R4863 T18667 T18657 punct .,correlated
R4864 T18669 T18670 csubj Screening,identified
R4865 T18671 T18672 det the,CSS
R4866 T18672 T18669 dobj CSS,Screening
R4867 T18673 T18674 nummod three,chromosomes
R4868 T18674 T18670 dobj chromosomes,identified
R4869 T18675 T18676 dep that,harbored
R4870 T18676 T18674 relcl harbored,chromosomes
R4871 T18677 T18676 dobj genes,harbored
R4872 T18678 T18679 dep which,contributed
R4873 T18679 T18677 relcl contributed,genes
R4874 T18680 T18679 prep to,contributed
R4875 T18681 T18682 det the,phenotype
R4876 T18682 T18680 pobj phenotype,to
R4877 T18683 T18684 compound A,J
R4878 T18684 T18682 compound J,phenotype
R4879 T18685 T18684 punct /,J
R4880 T18686 T18682 prep of,phenotype
R4881 T18687 T18688 amod increased,time
R4882 T18688 T18686 pobj time,of
R4883 T18689 T18688 compound rebleeding,time
R4884 T18690 T18670 punct .,identified
R4885 T18692 T18693 nsubjpass Mice,required
R4886 T18694 T18692 amod homosomic,Mice
R4887 T18695 T18694 prep for,homosomic
R4888 T18696 T18697 det these,chromosomes
R4889 T18697 T18695 pobj chromosomes,for
R4890 T18698 T18694 cc or,homosomic
R4891 T18699 T18700 advmod doubly,heterosomic
R4892 T18700 T18694 conj heterosomic,homosomic
R4893 T18701 T18700 prep for,heterosomic
R4894 T18702 T18701 pobj two,for
R4895 T18703 T18702 prep of,two
R4896 T18704 T18705 det the,chromosomes
R4897 T18705 T18703 pobj chromosomes,of
R4898 T18706 T18702 punct ", ",two
R4899 T18707 T18702 appos 5,two
R4900 T18708 T18707 cc and,5
R4901 T18709 T18707 conj 17,5
R4902 T18710 T18693 punct ", ",required
R4903 T18711 T18693 auxpass were,required
R4904 T18712 T18713 aux to,express
R4905 T18713 T18693 advcl express,required
R4906 T18714 T18715 det the,phenotype
R4907 T18715 T18713 dobj phenotype,express
R4908 T18716 T18717 compound A,J
R4909 T18717 T18715 compound J,phenotype
R4910 T18718 T18717 punct /,J
R4911 T18719 T18715 punct ", ",phenotype
R4912 T18720 T18721 amod elevated,time
R4913 T18721 T18715 appos time,phenotype
R4914 T18722 T18721 compound rebleeding,time
R4915 T18723 T18693 punct .,required
R4916 T18725 T18726 nsubjpass PAI,decreased
R4917 T18727 T18725 punct -,PAI
R4918 T18728 T18725 nummod 1,PAI
R4919 T18729 T18725 appos antigen,PAI
R4920 T18730 T18729 cc and,antigen
R4921 T18731 T18729 conj activity,antigen
R4922 T18732 T18726 auxpass were,decreased
R4923 T18733 T18726 prep in,decreased
R4924 T18734 T18735 preconj both,CSS
R4925 T18735 T18733 pobj CSS,in
R4926 T18736 T18735 punct -,CSS
R4927 T18737 T18735 nummod 5,CSS
R4928 T18738 T18735 cc and,CSS
R4929 T18739 T18735 conj CSS,CSS
R4930 T18740 T18739 punct -,CSS
R4931 T18741 T18739 nummod 17,CSS
R4932 T18742 T18735 cc and,CSS
R4933 T18743 T18744 det the,mice
R4934 T18744 T18735 conj mice,CSS
R4935 T18745 T18744 amod heterosomic,mice
R4936 T18746 T18744 punct ", ",mice
R4937 T18747 T18748 compound CSS,5F1
R4938 T18748 T18744 appos 5F1,mice
R4939 T18749 T18748 punct -,5F1
R4940 T18750 T18748 cc and,5F1
R4941 T18751 T18752 compound CSS,17F1
R4942 T18752 T18748 conj 17F1,5F1
R4943 T18753 T18752 punct -,17F1
R4944 T18754 T18733 punct ", ",in
R4945 T18755 T18733 cc but,in
R4946 T18756 T18755 neg not,but
R4947 T18757 T18733 conj in,in
R4948 T18758 T18759 det the,strain
R4949 T18759 T18757 pobj strain,in
R4950 T18760 T18759 nmod CSS,strain
R4951 T18761 T18760 punct -,CSS
R4952 T18762 T18760 nummod 11,CSS
R4953 T18763 T18726 punct .,decreased
R4954 T18765 T18766 nsubjpass Values,restored
R4955 T18767 T18766 auxpass were,restored
R4956 T18768 T18766 prep in,restored
R4957 T18769 T18770 det the,heterosomic
R4958 T18770 T18768 pobj heterosomic,in
R4959 T18771 T18770 advmod doubly,heterosomic
R4960 T18772 T18766 prep for,restored
R4961 T18773 T18772 pobj two,for
R4962 T18774 T18773 prep of,two
R4963 T18775 T18774 pobj chromosomes,of
R4964 T18776 T18773 punct ", ",two
R4965 T18777 T18773 appos 5,two
R4966 T18778 T18777 cc and,5
R4967 T18779 T18777 conj 17,5
R4968 T18780 T18766 punct .,restored
R4969 T18782 T18783 amod Arterial,occlusion
R4970 T18783 T18784 compound occlusion,time
R4971 T18784 T18785 nsubj time,was
R4972 T18786 T18785 acomp similar,was
R4973 T18787 T18786 prep to,similar
R4974 T18788 T18787 pobj B6,to
R4975 T18789 T18785 prep in,was
R4976 T18790 T18791 det the,strains
R4977 T18791 T18789 pobj strains,in
R4978 T18792 T18791 nmod CSS,strains
R4979 T18793 T18792 punct -,CSS
R4980 T18794 T18792 nummod 5,CSS
R4981 T18795 T18792 cc and,CSS
R4982 T18796 T18792 conj CSS,CSS
R4983 T18797 T18796 punct -,CSS
R4984 T18798 T18796 nummod 17,CSS
R4985 T18799 T18791 amod homozygous,strains
R4986 T18800 T18785 punct ", ",was
R4987 T18801 T18785 cc but,was
R4988 T18802 T18785 conj increased,was
R4989 T18803 T18802 prep in,increased
R4990 T18804 T18805 advmod doubly,heterosomic
R4991 T18805 T18803 pobj heterosomic,in
R4992 T18806 T18785 prep for,was
R4993 T18807 T18806 pobj two,for
R4994 T18808 T18807 prep of,two
R4995 T18809 T18808 pobj chromosomes,of
R4996 T18810 T18807 punct ", ",two
R4997 T18811 T18807 appos 5,two
R4998 T18812 T18811 cc and,5
R4999 T18813 T18811 conj 17,5
R5000 T18814 T18785 punct .,was