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PMC:509305 / 18321-19184 JSONTXT 4 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue
T8775 0-2 PRP denotes We
T8776 3-12 VBD denotes generated
T8777 13-14 DT denotes a
T8779 15-20 NN denotes C57BL
T8780 20-21 HYPH denotes /
T8781 21-22 CD denotes 6
T8782 23-31 JJ denotes congenic
T8778 32-36 NN denotes line
T8783 37-45 VBG denotes carrying
T8784 46-49 DT denotes the
T8786 50-59 JJ denotes telomeric
T8785 60-66 NN denotes region
T8787 67-69 IN denotes of
T8788 70-80 NN denotes Chromosome
T8789 81-82 CD denotes 1
T8790 83-87 IN denotes from
T8791 88-91 DT denotes the
T8793 92-95 CD denotes 129
T8794 96-101 NN denotes mouse
T8792 102-108 NN denotes strain
T8795 108-110 , denotes ,
T8796 110-112 IN denotes in
T8797 113-118 NN denotes order
T8798 119-121 TO denotes to
T8799 122-129 VB denotes dissect
T8800 130-133 DT denotes the
T8802 134-141 JJ denotes complex
T8803 142-151 JJ denotes polygenic
T8804 152-159 NN denotes disease
T8801 160-169 NN denotes phenotype
T8805 170-172 IN denotes of
T8806 173-176 DT denotes the
T8808 177-178 -LRB- denotes (
T8809 178-183 NN denotes C57BL
T8810 183-184 HYPH denotes /
T8811 184-185 CD denotes 6
T8812 186-187 SYM denotes ×
T8813 188-191 NN denotes 129
T8815 191-192 HYPH denotes /
T8814 192-194 NN denotes Sv
T8816 194-195 -RRB- denotes )
T8817 195-197 NN denotes F2
T8818 198-204 NN denotes hybrid
T8807 205-211 NN denotes strain
T8819 212-216 IN denotes into
T8820 217-220 PRP$ denotes its
T8822 221-231 JJ denotes individual
T8823 232-239 JJ denotes genetic
T8821 240-250 NNS denotes components
T8824 250-251 . denotes .
T8825 251-438 sentence denotes The 129 interval was backcrossed seven times onto C57BL/6, and at each generation the presence or absence of the Chromosome 1 interval was determined with several microsatellite markers.
T8826 252-255 DT denotes The
T8828 256-259 CD denotes 129
T8827 260-268 NN denotes interval
T8830 269-272 VBD denotes was
T8829 273-284 VBN denotes backcrossed
T8831 285-290 CD denotes seven
T8832 291-296 NNS denotes times
T8833 297-301 IN denotes onto
T8834 302-307 NN denotes C57BL
T8835 307-308 HYPH denotes /
T8836 308-309 CD denotes 6
T8837 309-311 , denotes ,
T8838 311-314 CC denotes and
T8839 315-317 IN denotes at
T8841 318-322 DT denotes each
T8842 323-333 NN denotes generation
T8843 334-337 DT denotes the
T8844 338-346 NN denotes presence
T8845 347-349 CC denotes or
T8846 350-357 NN denotes absence
T8847 358-360 IN denotes of
T8848 361-364 DT denotes the
T8850 365-375 NN denotes Chromosome
T8851 376-377 CD denotes 1
T8849 378-386 NN denotes interval
T8852 387-390 VBD denotes was
T8840 391-401 VBN denotes determined
T8853 402-406 IN denotes with
T8854 407-414 JJ denotes several
T8856 415-429 NN denotes microsatellite
T8855 430-437 NNS denotes markers
T8857 437-438 . denotes .
T8858 438-584 sentence denotes Each backcrossed generation was screened with more than three markers per chromosome to facilitate the removal of unselected 129 genomic regions.
T8859 439-443 DT denotes Each
T8861 444-455 VBN denotes backcrossed
T8860 456-466 NN denotes generation
T8863 467-470 VBD denotes was
T8862 471-479 VBN denotes screened
T8864 480-484 IN denotes with
T8865 485-489 JJR denotes more
T8867 490-494 IN denotes than
T8866 495-500 CD denotes three
T8868 501-508 NNS denotes markers
T8869 509-512 IN denotes per
T8870 513-523 NN denotes chromosome
T8871 524-526 TO denotes to
T8872 527-537 VB denotes facilitate
T8873 538-541 DT denotes the
T8874 542-549 NN denotes removal
T8875 550-552 IN denotes of
T8876 553-563 JJ denotes unselected
T8878 564-567 CD denotes 129
T8879 568-575 JJ denotes genomic
T8877 576-583 NNS denotes regions
T8880 583-584 . denotes .
T8881 584-863 sentence denotes At the end of the backcrossing, the 129-derived Chromosome 1 interval in the congenic mice extended from microsatellite marker D1Mit105 to D1Mit223 (80–106 cM), which encompasses the most important 129 interval identified by the linkage studies in the (C57BL/6 × 129/Sv)F2 mice.
T8882 585-587 IN denotes At
T8884 588-591 DT denotes the
T8885 592-595 NN denotes end
T8886 596-598 IN denotes of
T8887 599-602 DT denotes the
T8888 603-615 NN denotes backcrossing
T8889 615-617 , denotes ,
T8890 617-620 DT denotes the
T8892 621-624 CD denotes 129
T8894 624-625 HYPH denotes -
T8893 625-632 VBN denotes derived
T8895 633-643 NN denotes Chromosome
T8896 644-645 CD denotes 1
T8891 646-654 NN denotes interval
T8897 655-657 IN denotes in
T8898 658-661 DT denotes the
T8900 662-670 JJ denotes congenic
T8899 671-675 NNS denotes mice
T8883 676-684 VBN denotes extended
T8901 685-689 IN denotes from
T8902 690-704 NN denotes microsatellite
T8903 705-711 NN denotes marker
T8904 712-720 NN denotes D1Mit105
T8905 721-723 IN denotes to
T8906 724-732 NN denotes D1Mit223
T8907 733-734 -LRB- denotes (
T8909 734-736 CD denotes 80
T8911 736-737 SYM denotes –
T8910 737-740 CD denotes 106
T8908 741-743 NNS denotes cM
T8912 743-744 -RRB- denotes )
T8913 744-746 , denotes ,
T8914 746-751 WDT denotes which
T8915 752-763 VBZ denotes encompasses
T8916 764-767 DT denotes the
T8918 768-772 RBS denotes most
T8919 773-782 JJ denotes important
T8920 783-786 CD denotes 129
T8917 787-795 NN denotes interval
T8921 796-806 VBN denotes identified
T8922 807-809 IN denotes by
T8923 810-813 DT denotes the
T8925 814-821 NN denotes linkage
T8924 822-829 NNS denotes studies
T8926 830-832 IN denotes in
T8927 833-836 DT denotes the
T8929 837-838 -LRB- denotes (
T8930 838-843 NN denotes C57BL
T8931 843-844 HYPH denotes /
T8932 844-845 CD denotes 6
T8933 846-847 SYM denotes ×
T8934 848-851 NN denotes 129
T8936 851-852 HYPH denotes /
T8935 852-854 NN denotes Sv
T8937 854-855 -RRB- denotes )
T8938 855-857 NN denotes F2
T8928 858-862 NNS denotes mice
T8939 862-863 . denotes .
R2531 T8775 T8776 nsubj We,generated
R2532 T8777 T8778 det a,line
R2533 T8778 T8776 dobj line,generated
R2534 T8779 T8778 nmod C57BL,line
R2535 T8780 T8779 punct /,C57BL
R2536 T8781 T8779 nummod 6,C57BL
R2537 T8782 T8778 amod congenic,line
R2538 T8783 T8778 acl carrying,line
R2539 T8784 T8785 det the,region
R2540 T8785 T8783 dobj region,carrying
R2541 T8786 T8785 amod telomeric,region
R2542 T8787 T8785 prep of,region
R2543 T8788 T8787 pobj Chromosome,of
R2544 T8789 T8788 nummod 1,Chromosome
R2545 T8790 T8783 prep from,carrying
R2546 T8791 T8792 det the,strain
R2547 T8792 T8790 pobj strain,from
R2548 T8793 T8792 nummod 129,strain
R2549 T8794 T8792 compound mouse,strain
R2550 T8795 T8776 punct ", ",generated
R2551 T8796 T8776 prep in,generated
R2552 T8797 T8796 pobj order,in
R2553 T8798 T8799 aux to,dissect
R2554 T8799 T8797 acl dissect,order
R2555 T8800 T8801 det the,phenotype
R2556 T8801 T8799 dobj phenotype,dissect
R2557 T8802 T8801 amod complex,phenotype
R2558 T8803 T8801 amod polygenic,phenotype
R2559 T8804 T8801 compound disease,phenotype
R2560 T8805 T8801 prep of,phenotype
R2561 T8806 T8807 det the,strain
R2562 T8807 T8805 pobj strain,of
R2563 T8808 T8807 punct (,strain
R2564 T8809 T8807 nmod C57BL,strain
R2565 T8810 T8809 punct /,C57BL
R2566 T8811 T8809 nummod 6,C57BL
R2567 T8812 T8809 punct ×,C57BL
R2568 T8813 T8814 compound 129,Sv
R2569 T8814 T8809 appos Sv,C57BL
R2570 T8815 T8814 punct /,Sv
R2571 T8816 T8807 punct ),strain
R2572 T8817 T8807 compound F2,strain
R2573 T8818 T8807 compound hybrid,strain
R2574 T8819 T8799 prep into,dissect
R2575 T8820 T8821 poss its,components
R2576 T8821 T8819 pobj components,into
R2577 T8822 T8821 amod individual,components
R2578 T8823 T8821 amod genetic,components
R2579 T8824 T8776 punct .,generated
R2580 T8826 T8827 det The,interval
R2581 T8827 T8829 nsubjpass interval,backcrossed
R2582 T8828 T8827 nummod 129,interval
R2583 T8830 T8829 auxpass was,backcrossed
R2584 T8831 T8832 nummod seven,times
R2585 T8832 T8829 npadvmod times,backcrossed
R2586 T8833 T8829 prep onto,backcrossed
R2587 T8834 T8833 pobj C57BL,onto
R2588 T8835 T8834 punct /,C57BL
R2589 T8836 T8834 nummod 6,C57BL
R2590 T8837 T8829 punct ", ",backcrossed
R2591 T8838 T8829 cc and,backcrossed
R2592 T8839 T8840 prep at,determined
R2593 T8840 T8829 conj determined,backcrossed
R2594 T8841 T8842 det each,generation
R2595 T8842 T8839 pobj generation,at
R2596 T8843 T8844 det the,presence
R2597 T8844 T8840 nsubjpass presence,determined
R2598 T8845 T8844 cc or,presence
R2599 T8846 T8844 conj absence,presence
R2600 T8847 T8844 prep of,presence
R2601 T8848 T8849 det the,interval
R2602 T8849 T8847 pobj interval,of
R2603 T8850 T8849 nmod Chromosome,interval
R2604 T8851 T8850 nummod 1,Chromosome
R2605 T8852 T8840 auxpass was,determined
R2606 T8853 T8840 prep with,determined
R2607 T8854 T8855 amod several,markers
R2608 T8855 T8853 pobj markers,with
R2609 T8856 T8855 compound microsatellite,markers
R2610 T8857 T8840 punct .,determined
R2611 T8859 T8860 det Each,generation
R2612 T8860 T8862 nsubjpass generation,screened
R2613 T8861 T8860 amod backcrossed,generation
R2614 T8863 T8862 auxpass was,screened
R2615 T8864 T8862 prep with,screened
R2616 T8865 T8866 amod more,three
R2617 T8866 T8868 nummod three,markers
R2618 T8867 T8866 quantmod than,three
R2619 T8868 T8864 pobj markers,with
R2620 T8869 T8868 prep per,markers
R2621 T8870 T8869 pobj chromosome,per
R2622 T8871 T8872 aux to,facilitate
R2623 T8872 T8862 advcl facilitate,screened
R2624 T8873 T8874 det the,removal
R2625 T8874 T8872 dobj removal,facilitate
R2626 T8875 T8874 prep of,removal
R2627 T8876 T8877 amod unselected,regions
R2628 T8877 T8875 pobj regions,of
R2629 T8878 T8877 nummod 129,regions
R2630 T8879 T8877 amod genomic,regions
R2631 T8880 T8862 punct .,screened
R2632 T8882 T8883 prep At,extended
R2633 T8884 T8885 det the,end
R2634 T8885 T8882 pobj end,At
R2635 T8886 T8885 prep of,end
R2636 T8887 T8888 det the,backcrossing
R2637 T8888 T8886 pobj backcrossing,of
R2638 T8889 T8883 punct ", ",extended
R2639 T8890 T8891 det the,interval
R2640 T8891 T8883 nsubj interval,extended
R2641 T8892 T8893 advmod 129,derived
R2642 T8893 T8891 amod derived,interval
R2643 T8894 T8893 punct -,derived
R2644 T8895 T8891 nmod Chromosome,interval
R2645 T8896 T8895 nummod 1,Chromosome
R2646 T8897 T8891 prep in,interval
R2647 T8898 T8899 det the,mice
R2648 T8899 T8897 pobj mice,in
R2649 T8900 T8899 amod congenic,mice
R2650 T8901 T8883 prep from,extended
R2651 T8902 T8903 compound microsatellite,marker
R2652 T8903 T8901 pobj marker,from
R2653 T8904 T8903 appos D1Mit105,marker
R2654 T8905 T8901 prep to,from
R2655 T8906 T8905 pobj D1Mit223,to
R2656 T8907 T8908 punct (,cM
R2657 T8908 T8906 parataxis cM,D1Mit223
R2658 T8909 T8910 quantmod 80,106
R2659 T8910 T8908 nummod 106,cM
R2660 T8911 T8910 punct –,106
R2661 T8912 T8908 punct ),cM
R2662 T8913 T8883 punct ", ",extended
R2663 T8914 T8915 dep which,encompasses
R2664 T8915 T8883 advcl encompasses,extended
R2665 T8916 T8917 det the,interval
R2666 T8917 T8915 dobj interval,encompasses
R2667 T8918 T8919 advmod most,important
R2668 T8919 T8917 amod important,interval
R2669 T8920 T8917 nummod 129,interval
R2670 T8921 T8917 acl identified,interval
R2671 T8922 T8921 agent by,identified
R2672 T8923 T8924 det the,studies
R2673 T8924 T8922 pobj studies,by
R2674 T8925 T8924 compound linkage,studies
R2675 T8926 T8921 prep in,identified
R2676 T8927 T8928 det the,mice
R2677 T8928 T8926 pobj mice,in
R2678 T8929 T8928 punct (,mice
R2679 T8930 T8928 nmod C57BL,mice
R2680 T8931 T8930 punct /,C57BL
R2681 T8932 T8930 nummod 6,C57BL
R2682 T8933 T8930 punct ×,C57BL
R2683 T8934 T8935 compound 129,Sv
R2684 T8935 T8930 appos Sv,C57BL
R2685 T8936 T8935 punct /,Sv
R2686 T8937 T8928 punct ),mice
R2687 T8938 T8928 compound F2,mice
R2688 T8939 T8883 punct .,extended