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PMC:1584416 / 29607-30120 JSONTXT 5 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue
T5614 0-8 RB denotes Recently
T5616 8-10 , denotes ,
T5617 10-18 NN denotes proteins
T5618 19-30 VBG denotes originating
T5619 31-35 IN denotes from
T5620 36-44 VBN denotes presumed
T5622 45-49 JJ denotes null
T5621 50-57 NNS denotes alleles
T5623 58-62 VBD denotes were
T5624 63-76 RB denotes biochemically
T5615 77-90 VBN denotes characterised
T5625 91-93 IN denotes as
T5626 94-102 JJ denotes inactive
T5627 103-105 IN denotes in
T5628 106-111 JJ denotes basal
T5629 112-125 NN denotes transcription
T5630 126-127 -LRB- denotes [
T5631 127-129 CD denotes 27
T5632 129-130 -RRB- denotes ]
T5633 130-132 , denotes ,
T5634 132-141 VBG denotes providing
T5635 142-144 DT denotes an
T5636 145-156 NN denotes explanation
T5637 157-159 IN denotes as
T5638 160-162 IN denotes to
T5639 163-166 WRB denotes why
T5641 167-172 DT denotes these
T5642 173-180 NNS denotes alleles
T5640 181-187 VBD denotes failed
T5643 188-190 TO denotes to
T5644 191-197 VB denotes rescue
T5645 198-207 NN denotes lethality
T5646 208-210 IN denotes in
T5647 211-218 JJ denotes haploid
T5649 219-221 FW denotes S.
T5648 222-227 FW denotes pombe
T5650 228-232 IN denotes with
T5651 233-234 DT denotes a
T5653 235-239 JJ denotes null
T5652 240-248 NN denotes mutation
T5654 249-251 IN denotes in
T5655 252-255 DT denotes the
T5657 256-259 NN denotes XPD
T5656 260-269 NN denotes homologue
T5658 270-275 NN denotes rad15
T5659 276-277 -LRB- denotes [
T5660 277-279 CD denotes 19
T5661 279-280 -RRB- denotes ]
T5662 280-281 . denotes .
T5663 281-513 sentence denotes Our data suggest that certain presumed null alleles, although unable on their own to support basal transcription, may in fact have a substantial impact on disease outcome in compound heterozygous humans, as they do in mouse models.
T5664 282-285 PRP$ denotes Our
T5665 286-290 NNS denotes data
T5666 291-298 VBP denotes suggest
T5667 299-303 IN denotes that
T5669 304-311 JJ denotes certain
T5671 312-320 VBN denotes presumed
T5672 321-325 JJ denotes null
T5670 326-333 NNS denotes alleles
T5673 333-335 , denotes ,
T5674 335-343 IN denotes although
T5675 344-350 JJ denotes unable
T5676 351-353 IN denotes on
T5678 354-359 PRP$ denotes their
T5679 360-363 NN denotes own
T5680 364-366 TO denotes to
T5677 367-374 VB denotes support
T5681 375-380 JJ denotes basal
T5682 381-394 NN denotes transcription
T5683 394-396 , denotes ,
T5684 396-399 MD denotes may
T5685 400-402 IN denotes in
T5686 403-407 NN denotes fact
T5668 408-412 VB denotes have
T5687 413-414 DT denotes a
T5689 415-426 JJ denotes substantial
T5688 427-433 NN denotes impact
T5690 434-436 IN denotes on
T5691 437-444 NN denotes disease
T5692 445-452 NN denotes outcome
T5693 453-455 IN denotes in
T5694 456-464 NN denotes compound
T5696 465-477 JJ denotes heterozygous
T5695 478-484 NNS denotes humans
T5697 484-486 , denotes ,
T5698 486-488 IN denotes as
T5700 489-493 PRP denotes they
T5701 494-496 VBP denotes do
T5699 497-499 IN denotes in
T5702 500-505 NN denotes mouse
T5703 506-512 NNS denotes models
T5704 512-513 . denotes .
R3760 T5614 T5615 advmod Recently,characterised
R3761 T5616 T5615 punct ", ",characterised
R3762 T5617 T5615 nsubjpass proteins,characterised
R3763 T5618 T5617 acl originating,proteins
R3764 T5619 T5618 prep from,originating
R3765 T5620 T5621 amod presumed,alleles
R3766 T5621 T5619 pobj alleles,from
R3767 T5622 T5621 amod null,alleles
R3768 T5623 T5615 auxpass were,characterised
R3769 T5624 T5615 advmod biochemically,characterised
R3770 T5625 T5615 prep as,characterised
R3771 T5626 T5625 amod inactive,as
R3772 T5627 T5615 prep in,characterised
R3773 T5628 T5629 amod basal,transcription
R3774 T5629 T5627 pobj transcription,in
R3775 T5630 T5631 punct [,27
R3776 T5631 T5615 parataxis 27,characterised
R3777 T5632 T5631 punct ],27
R3778 T5633 T5615 punct ", ",characterised
R3779 T5634 T5615 advcl providing,characterised
R3780 T5635 T5636 det an,explanation
R3781 T5636 T5634 dobj explanation,providing
R3782 T5637 T5636 prep as,explanation
R3783 T5638 T5637 prep to,as
R3784 T5639 T5640 advmod why,failed
R3785 T5640 T5638 pcomp failed,to
R3786 T5641 T5642 det these,alleles
R3787 T5642 T5640 nsubj alleles,failed
R3788 T5643 T5644 aux to,rescue
R3789 T5644 T5640 xcomp rescue,failed
R3790 T5645 T5644 dobj lethality,rescue
R3791 T5646 T5644 prep in,rescue
R3792 T5647 T5648 amod haploid,pombe
R3793 T5648 T5646 pobj pombe,in
R3794 T5649 T5648 nmod S.,pombe
R3795 T5650 T5648 prep with,pombe
R3796 T5651 T5652 det a,mutation
R3797 T5652 T5650 pobj mutation,with
R3798 T5653 T5652 amod null,mutation
R3799 T5654 T5652 prep in,mutation
R3800 T5655 T5656 det the,homologue
R3801 T5656 T5654 pobj homologue,in
R3802 T5657 T5656 compound XPD,homologue
R3803 T5658 T5656 appos rad15,homologue
R3804 T5659 T5660 punct [,19
R3805 T5660 T5640 parataxis 19,failed
R3806 T5661 T5660 punct ],19
R3807 T5662 T5615 punct .,characterised
R3808 T5664 T5665 poss Our,data
R3809 T5665 T5666 nsubj data,suggest
R3810 T5667 T5668 mark that,have
R3811 T5668 T5666 ccomp have,suggest
R3812 T5669 T5670 amod certain,alleles
R3813 T5670 T5668 nsubj alleles,have
R3814 T5671 T5672 advmod presumed,null
R3815 T5672 T5670 amod null,alleles
R3816 T5673 T5668 punct ", ",have
R3817 T5674 T5675 mark although,unable
R3818 T5675 T5668 advcl unable,have
R3819 T5676 T5677 prep on,support
R3820 T5677 T5675 xcomp support,unable
R3821 T5678 T5679 poss their,own
R3822 T5679 T5676 pobj own,on
R3823 T5680 T5677 aux to,support
R3824 T5681 T5682 amod basal,transcription
R3825 T5682 T5677 dobj transcription,support
R3826 T5683 T5668 punct ", ",have
R3827 T5684 T5668 aux may,have
R3828 T5685 T5668 prep in,have
R3829 T5686 T5685 pobj fact,in
R3830 T5687 T5688 det a,impact
R3831 T5688 T5668 dobj impact,have
R3832 T5689 T5688 amod substantial,impact
R3833 T5690 T5688 prep on,impact
R3834 T5691 T5692 compound disease,outcome
R3835 T5692 T5690 pobj outcome,on
R3836 T5693 T5688 prep in,impact
R3837 T5694 T5695 nmod compound,humans
R3838 T5695 T5693 pobj humans,in
R3839 T5696 T5695 amod heterozygous,humans
R3840 T5697 T5668 punct ", ",have
R3841 T5698 T5699 mark as,in
R3842 T5699 T5668 advcl in,have
R3843 T5700 T5699 nsubj they,in
R3844 T5701 T5699 aux do,in
R3845 T5702 T5703 compound mouse,models
R3846 T5703 T5699 pobj models,in
R3847 T5704 T5666 punct .,suggest