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PMC:1440874 / 48535-49070 JSONTXT

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craft-sa-dev

Id Subject Object Predicate Lexical cue
T10729 0-7 DT denotes Another
T10730 17-26 NN denotes mechanism
T10731 8-16 JJ denotes possible
T10732 27-29 VBZ denotes is
T10733 30-34 IN denotes that
T10734 66-74 VBZ denotes proceeds
T10735 35-47 NN denotes inactivation
T10736 48-50 IN denotes of
T10737 51-54 DT denotes the
T10738 64-65 NN denotes X
T10739 55-63 JJ denotes paternal
T10740 75-83 RB denotes normally
T10741 84-86 IN denotes in
T10742 87-90 DT denotes all
T10743 91-96 NNS denotes cells
T10744 96-98 , denotes ,
T10745 98-101 CC denotes but
T10746 102-114 RB denotes subsequently
T10747 156-167 VBN denotes reactivated
T10748 115-118 DT denotes the
T10749 124-128 NN denotes gene
T10750 119-123 NN denotes Atrx
T10751 129-135 IN denotes within
T10752 136-146 JJ denotes individual
T10753 147-152 NNS denotes cells
T10754 153-155 VBZ denotes is
T10755 167-168 . denotes .
T10756 168-281 sentence denotes Alternatively, in the absence of Atrx, the paternal allele may partially escape the normal process of silencing.
T10757 169-182 RB denotes Alternatively
T10758 242-248 VB denotes escape
T10759 182-184 , denotes ,
T10760 184-186 IN denotes in
T10761 187-190 DT denotes the
T10762 191-198 NN denotes absence
T10763 199-201 IN denotes of
T10764 202-206 NN denotes Atrx
T10765 206-208 , denotes ,
T10766 208-211 DT denotes the
T10767 221-227 NN denotes allele
T10768 212-220 JJ denotes paternal
T10769 228-231 MD denotes may
T10770 232-241 RB denotes partially
T10771 249-252 DT denotes the
T10772 260-267 NN denotes process
T10773 253-259 JJ denotes normal
T10774 268-270 IN denotes of
T10775 271-280 NN denotes silencing
T10776 280-281 . denotes .
T10777 281-535 sentence denotes In both of these cases, other genes on the paternal X chromosome must be inactivated and remain so, since blocking inactivation of the entire Xp chromosome causes embryonic lethality due to biallelic expression of X-linked genes in the trophoblast [39].
T10778 282-284 IN denotes In
T10779 355-366 VBN denotes inactivated
T10780 285-289 DT denotes both
T10781 290-292 IN denotes of
T10782 293-298 DT denotes these
T10783 299-304 NNS denotes cases
T10784 304-306 , denotes ,
T10785 306-311 JJ denotes other
T10786 312-317 NNS denotes genes
T10787 318-320 IN denotes on
T10788 321-324 DT denotes the
T10789 336-346 NN denotes chromosome
T10790 325-333 JJ denotes paternal
T10791 334-335 NN denotes X
T10792 347-351 MD denotes must
T10793 352-354 VB denotes be
T10794 367-370 CC denotes and
T10795 371-377 VBP denotes remain
T10796 378-380 RB denotes so
T10797 380-382 , denotes ,
T10798 382-387 IN denotes since
T10799 438-444 VBZ denotes causes
T10800 388-396 VBG denotes blocking
T10801 397-409 NN denotes inactivation
T10802 410-412 IN denotes of
T10803 413-416 DT denotes the
T10804 427-437 NN denotes chromosome
T10805 417-423 JJ denotes entire
T10806 424-426 NN denotes Xp
T10807 445-454 JJ denotes embryonic
T10808 455-464 NN denotes lethality
T10809 465-468 IN denotes due
T10810 469-471 IN denotes to
T10811 472-481 JJ denotes biallelic
T10812 482-492 NN denotes expression
T10813 493-495 IN denotes of
T10814 496-497 NN denotes X
T10815 498-504 VBN denotes linked
T10816 497-498 HYPH denotes -
T10817 505-510 NNS denotes genes
T10818 511-513 IN denotes in
T10819 514-517 DT denotes the
T10820 518-529 NN denotes trophoblast
T10821 530-531 -LRB- denotes [
T10822 531-533 CD denotes 39
T10823 533-534 -RRB- denotes ]
T10824 534-535 . denotes .
R6682 T10729 T10730 det Another,mechanism
R6683 T10730 T10732 nsubj mechanism,is
R6684 T10731 T10730 amod possible,mechanism
R6685 T10733 T10734 mark that,proceeds
R6686 T10734 T10732 ccomp proceeds,is
R6687 T10735 T10734 nsubj inactivation,proceeds
R6688 T10736 T10735 prep of,inactivation
R6689 T10737 T10738 det the,X
R6690 T10738 T10736 pobj X,of
R6691 T10739 T10738 amod paternal,X
R6692 T10740 T10734 advmod normally,proceeds
R6693 T10741 T10734 prep in,proceeds
R6694 T10742 T10743 det all,cells
R6695 T10743 T10741 pobj cells,in
R6696 T10744 T10734 punct ", ",proceeds
R6697 T10745 T10734 cc but,proceeds
R6698 T10746 T10747 advmod subsequently,reactivated
R6699 T10747 T10734 conj reactivated,proceeds
R6700 T10748 T10749 det the,gene
R6701 T10749 T10747 nsubjpass gene,reactivated
R6702 T10750 T10749 compound Atrx,gene
R6703 T10751 T10749 prep within,gene
R6704 T10752 T10753 amod individual,cells
R6705 T10753 T10751 pobj cells,within
R6706 T10754 T10747 auxpass is,reactivated
R6707 T10755 T10732 punct .,is
R6708 T10757 T10758 advmod Alternatively,escape
R6709 T10759 T10758 punct ", ",escape
R6710 T10760 T10758 prep in,escape
R6711 T10761 T10762 det the,absence
R6712 T10762 T10760 pobj absence,in
R6713 T10763 T10762 prep of,absence
R6714 T10764 T10763 pobj Atrx,of
R6715 T10765 T10758 punct ", ",escape
R6716 T10766 T10767 det the,allele
R6717 T10767 T10758 nsubj allele,escape
R6718 T10768 T10767 amod paternal,allele
R6719 T10769 T10758 aux may,escape
R6720 T10770 T10758 advmod partially,escape
R6721 T10771 T10772 det the,process
R6722 T10772 T10758 dobj process,escape
R6723 T10773 T10772 amod normal,process
R6724 T10774 T10772 prep of,process
R6725 T10775 T10774 pobj silencing,of
R6726 T10776 T10758 punct .,escape
R6727 T10778 T10779 prep In,inactivated
R6728 T10780 T10778 pobj both,In
R6729 T10781 T10780 prep of,both
R6730 T10782 T10783 det these,cases
R6731 T10783 T10781 pobj cases,of
R6732 T10784 T10779 punct ", ",inactivated
R6733 T10785 T10786 amod other,genes
R6734 T10786 T10779 nsubjpass genes,inactivated
R6735 T10787 T10786 prep on,genes
R6736 T10788 T10789 det the,chromosome
R6737 T10789 T10787 pobj chromosome,on
R6738 T10790 T10789 amod paternal,chromosome
R6739 T10791 T10789 compound X,chromosome
R6740 T10792 T10779 aux must,inactivated
R6741 T10793 T10779 auxpass be,inactivated
R6742 T10794 T10779 cc and,inactivated
R6743 T10795 T10779 conj remain,inactivated
R6744 T10796 T10795 advmod so,remain
R6745 T10797 T10779 punct ", ",inactivated
R6746 T10798 T10799 mark since,causes
R6747 T10799 T10779 advcl causes,inactivated
R6748 T10800 T10801 amod blocking,inactivation
R6749 T10801 T10799 nsubj inactivation,causes
R6750 T10802 T10801 prep of,inactivation
R6751 T10803 T10804 det the,chromosome
R6752 T10804 T10802 pobj chromosome,of
R6753 T10805 T10804 amod entire,chromosome
R6754 T10806 T10804 compound Xp,chromosome
R6755 T10807 T10808 amod embryonic,lethality
R6756 T10808 T10799 dobj lethality,causes
R6757 T10809 T10799 prep due,causes
R6758 T10810 T10809 pcomp to,due
R6759 T10811 T10812 amod biallelic,expression
R6760 T10812 T10809 pobj expression,due
R6761 T10813 T10812 prep of,expression
R6762 T10814 T10815 npadvmod X,linked
R6763 T10815 T10817 amod linked,genes
R6764 T10816 T10815 punct -,linked
R6765 T10817 T10813 pobj genes,of
R6766 T10818 T10812 prep in,expression
R6767 T10819 T10820 det the,trophoblast
R6768 T10820 T10818 pobj trophoblast,in
R6769 T10821 T10822 punct [,39
R6770 T10822 T10779 parataxis 39,inactivated
R6771 T10823 T10822 punct ],39
R6772 T10824 T10779 punct .,inactivated

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
T9909 35-50 _FRAGMENT denotes inactivation of
T9910 55-65 GO:0060817 denotes paternal X
T9911 64-65 GO:0000805 denotes X
T9912 91-96 CL_GO_EXT:cell denotes cells
T9913 119-123 PR_EXT:000004503 denotes Atrx
T9914 124-128 SO_EXT:0000704 denotes gene
T9915 147-152 CL_GO_EXT:cell denotes cells
T9916 202-206 PR_EXT:000004503 denotes Atrx
T9917 221-227 SO_EXT:0001023 denotes allele
T9918 271-280 GO:0016458 denotes silencing
T9919 312-317 SO_EXT:0000704 denotes genes
T9920 334-346 GO:0000805 denotes X chromosome
T9921 336-346 GO_SO_EXT:chromosome denotes chromosome
T9922 397-412 _FRAGMENT denotes inactivation of
T9923 424-437 GO:0060817 denotes Xp chromosome
T9924 427-437 GO_SO_EXT:chromosome denotes chromosome
T9925 445-454 UBERON:0000922 denotes embryonic
T9926 455-464 GO_EXT:fatality_or_lethality denotes lethality
T9927 474-481 SO_EXT:0001023 denotes allelic
T9928 482-492 GO:0010467 denotes expression
T9929 496-497 GO:0000805 denotes X
T9930 505-510 SO_EXT:0000704 denotes genes
T9931 518-529 UBERON:0000088 denotes trophoblast
R5925 T9910 T9909 _lexicallyChainedTo paternal X,inactivation of
R5926 T9923 T9922 _lexicallyChainedTo Xp chromosome,inactivation of

2_test

Id Subject Object Predicate Lexical cue
16628246-9009199-85799783 531-533 9009199 denotes 39
T9506 531-533 9009199 denotes 39

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
T9710 35-50 _FRAGMENT denotes inactivation of
T9711 55-65 GO:0060817 denotes paternal X
T9712 64-65 GO:0000805 denotes X
T9713 119-123 PR:000004503 denotes Atrx
T9714 124-128 SO:0000704 denotes gene
T9715 202-206 PR:000004503 denotes Atrx
T9716 221-227 SO:0001023 denotes allele
T9717 271-280 GO:0016458 denotes silencing
T9718 312-317 SO:0000704 denotes genes
T9719 334-346 GO:0000805 denotes X chromosome
T9720 397-412 _FRAGMENT denotes inactivation of
T9721 424-437 GO:0060817 denotes Xp chromosome
T9722 445-454 UBERON:0000922 denotes embryonic
T9723 474-481 SO:0001023 denotes allelic
T9724 482-492 GO:0010467 denotes expression
T9725 496-497 GO:0000805 denotes X
T9726 505-510 SO:0000704 denotes genes
T9727 518-529 UBERON:0000088 denotes trophoblast
R5916 T9711 T9710 _lexicallyChainedTo paternal X,inactivation of
R5917 T9721 T9720 _lexicallyChainedTo Xp chromosome,inactivation of