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PMC:1440874 / 2868-3662 JSONTXT 5 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue
T722 0-3 NN denotes ATR
T724 3-4 HYPH denotes -
T723 4-5 NN denotes X
T725 6-14 NN denotes syndrome
T726 15-17 VBZ denotes is
T727 18-19 DT denotes a
T729 20-26 JJ denotes severe
T730 26-28 , denotes ,
T731 28-42 JJ denotes nonprogressive
T728 43-47 NN denotes form
T732 48-50 IN denotes of
T733 51-52 NN denotes X
T735 52-53 HYPH denotes -
T734 53-59 VBN denotes linked
T737 60-66 JJ denotes mental
T736 67-78 NN denotes retardation
T738 79-83 WDT denotes that
T740 84-86 VBZ denotes is
T741 87-97 RB denotes frequently
T739 98-108 VBN denotes associated
T742 109-113 IN denotes with
T743 114-122 JJ denotes multiple
T745 123-133 JJ denotes congenital
T744 134-147 NNS denotes abnormalities
T746 148-149 -LRB- denotes [
T747 149-150 CD denotes 1
T748 150-151 -RRB- denotes ]
T749 151-152 . denotes .
T750 152-401 sentence denotes It is usually associated with a mild form of α-thalassaemia, caused by reduced expression of structurally intact α-globin genes, and characterised by the presence of β-globin tetramers (haemoglobin H inclusion bodies) in peripheral red blood cells.
T751 153-155 PRP denotes It
T753 156-158 VBZ denotes is
T754 159-166 RB denotes usually
T752 167-177 VBN denotes associated
T755 178-182 IN denotes with
T756 183-184 DT denotes a
T758 185-189 JJ denotes mild
T757 190-194 NN denotes form
T759 195-197 IN denotes of
T760 198-199 NN denotes α
T762 199-200 HYPH denotes -
T761 200-212 NN denotes thalassaemia
T763 212-214 , denotes ,
T764 214-220 VBN denotes caused
T765 221-223 IN denotes by
T766 224-231 VBN denotes reduced
T767 232-242 NN denotes expression
T768 243-245 IN denotes of
T769 246-258 RB denotes structurally
T770 259-265 JJ denotes intact
T772 266-267 NN denotes α
T774 267-268 HYPH denotes -
T773 268-274 NN denotes globin
T771 275-280 NNS denotes genes
T775 280-282 , denotes ,
T776 282-285 CC denotes and
T777 286-299 VBN denotes characterised
T778 300-302 IN denotes by
T779 303-306 DT denotes the
T780 307-315 NN denotes presence
T781 316-318 IN denotes of
T782 319-320 NN denotes β
T784 320-321 HYPH denotes -
T783 321-327 NN denotes globin
T785 328-337 NNS denotes tetramers
T786 338-339 -LRB- denotes (
T787 339-350 NN denotes haemoglobin
T788 351-352 NN denotes H
T790 353-362 NN denotes inclusion
T789 363-369 NNS denotes bodies
T791 369-370 -RRB- denotes )
T792 371-373 IN denotes in
T793 374-384 JJ denotes peripheral
T795 385-388 JJ denotes red
T796 389-394 NN denotes blood
T794 395-400 NNS denotes cells
T797 400-401 . denotes .
T798 401-521 sentence denotes Carrier females occasionally manifest haemoglobin H inclusions, but are otherwise intellectually and physically normal.
T799 402-409 NN denotes Carrier
T800 410-417 NNS denotes females
T802 418-430 RB denotes occasionally
T801 431-439 VBP denotes manifest
T803 440-451 NN denotes haemoglobin
T804 452-453 NN denotes H
T805 454-464 NNS denotes inclusions
T806 464-466 , denotes ,
T807 466-469 CC denotes but
T808 470-473 VBP denotes are
T809 474-483 RB denotes otherwise
T810 484-498 RB denotes intellectually
T812 499-502 CC denotes and
T813 503-513 RB denotes physically
T811 514-520 JJ denotes normal
T814 520-521 . denotes .
T815 521-794 sentence denotes Studies of X-chromosome inactivation in carrier females have demonstrated preferential inactivation of the chromosome bearing the abnormal allele in a variety of tissues [2], and this skewing of X-inactivation is thought to explain the mild phenotype observed in carriers.
T816 522-529 NNS denotes Studies
T818 530-532 IN denotes of
T819 533-534 NN denotes X
T821 534-535 HYPH denotes -
T820 535-545 NN denotes chromosome
T822 546-558 NN denotes inactivation
T823 559-561 IN denotes in
T824 562-569 NN denotes carrier
T825 570-577 NNS denotes females
T826 578-582 VBP denotes have
T817 583-595 VBN denotes demonstrated
T827 596-608 JJ denotes preferential
T828 609-621 NN denotes inactivation
T829 622-624 IN denotes of
T830 625-628 DT denotes the
T831 629-639 NN denotes chromosome
T832 640-647 VBG denotes bearing
T833 648-651 DT denotes the
T835 652-660 JJ denotes abnormal
T834 661-667 NN denotes allele
T836 668-670 IN denotes in
T837 671-672 DT denotes a
T838 673-680 NN denotes variety
T839 681-683 IN denotes of
T840 684-691 NNS denotes tissues
T841 692-693 -LRB- denotes [
T842 693-694 CD denotes 2
T843 694-695 -RRB- denotes ]
T844 695-697 , denotes ,
T845 697-700 CC denotes and
T846 701-705 DT denotes this
T847 706-713 NN denotes skewing
T849 714-716 IN denotes of
T850 717-718 NN denotes X
T852 718-719 HYPH denotes -
T851 719-731 NN denotes inactivation
T853 732-734 VBZ denotes is
T848 735-742 VBN denotes thought
T854 743-745 TO denotes to
T855 746-753 VB denotes explain
T856 754-757 DT denotes the
T858 758-762 JJ denotes mild
T857 763-772 NN denotes phenotype
T859 773-781 VBN denotes observed
T860 782-784 IN denotes in
T861 785-793 NNS denotes carriers
T862 793-794 . denotes .
R249 T722 T723 compound ATR,X
R250 T723 T725 compound X,syndrome
R251 T724 T723 punct -,X
R252 T725 T726 nsubj syndrome,is
R253 T727 T728 det a,form
R254 T728 T726 attr form,is
R255 T729 T728 amod severe,form
R256 T730 T728 punct ", ",form
R257 T731 T728 amod nonprogressive,form
R258 T732 T728 prep of,form
R259 T733 T734 npadvmod X,linked
R260 T734 T736 amod linked,retardation
R261 T735 T734 punct -,linked
R262 T736 T732 pobj retardation,of
R263 T737 T736 amod mental,retardation
R264 T738 T739 dep that,associated
R265 T739 T728 relcl associated,form
R266 T740 T739 auxpass is,associated
R267 T741 T739 advmod frequently,associated
R268 T742 T739 prep with,associated
R269 T743 T744 amod multiple,abnormalities
R270 T744 T742 pobj abnormalities,with
R271 T745 T744 amod congenital,abnormalities
R272 T746 T747 punct [,1
R273 T747 T726 parataxis 1,is
R274 T748 T747 punct ],1
R275 T749 T726 punct .,is
R276 T751 T752 nsubjpass It,associated
R277 T753 T752 auxpass is,associated
R278 T754 T752 advmod usually,associated
R279 T755 T752 prep with,associated
R280 T756 T757 det a,form
R281 T757 T755 pobj form,with
R282 T758 T757 amod mild,form
R283 T759 T757 prep of,form
R284 T760 T761 compound α,thalassaemia
R285 T761 T759 pobj thalassaemia,of
R286 T762 T761 punct -,thalassaemia
R287 T763 T757 punct ", ",form
R288 T764 T757 acl caused,form
R289 T765 T764 agent by,caused
R290 T766 T767 amod reduced,expression
R291 T767 T765 pobj expression,by
R292 T768 T767 prep of,expression
R293 T769 T770 advmod structurally,intact
R294 T770 T771 amod intact,genes
R295 T771 T768 pobj genes,of
R296 T772 T773 compound α,globin
R297 T773 T771 compound globin,genes
R298 T774 T773 punct -,globin
R299 T775 T752 punct ", ",associated
R300 T776 T752 cc and,associated
R301 T777 T752 conj characterised,associated
R302 T778 T777 prep by,characterised
R303 T779 T780 det the,presence
R304 T780 T778 pobj presence,by
R305 T781 T780 prep of,presence
R306 T782 T783 compound β,globin
R307 T783 T785 compound globin,tetramers
R308 T784 T783 punct -,globin
R309 T785 T781 pobj tetramers,of
R310 T786 T785 punct (,tetramers
R311 T787 T788 compound haemoglobin,H
R312 T788 T789 compound H,bodies
R313 T789 T785 appos bodies,tetramers
R314 T790 T789 compound inclusion,bodies
R315 T791 T780 punct ),presence
R316 T792 T780 prep in,presence
R317 T793 T794 amod peripheral,cells
R318 T794 T792 pobj cells,in
R319 T795 T794 amod red,cells
R320 T796 T794 compound blood,cells
R321 T797 T752 punct .,associated
R322 T799 T800 compound Carrier,females
R323 T800 T801 nsubj females,manifest
R324 T802 T801 advmod occasionally,manifest
R325 T803 T804 compound haemoglobin,H
R326 T804 T805 compound H,inclusions
R327 T805 T801 dobj inclusions,manifest
R328 T806 T801 punct ", ",manifest
R329 T807 T801 cc but,manifest
R330 T808 T801 conj are,manifest
R331 T809 T808 advmod otherwise,are
R332 T810 T811 advmod intellectually,normal
R333 T811 T808 acomp normal,are
R334 T812 T810 cc and,intellectually
R335 T813 T810 conj physically,intellectually
R336 T814 T801 punct .,manifest
R337 T816 T817 nsubj Studies,demonstrated
R338 T818 T816 prep of,Studies
R339 T819 T820 compound X,chromosome
R340 T820 T822 compound chromosome,inactivation
R341 T821 T820 punct -,chromosome
R342 T822 T818 pobj inactivation,of
R343 T823 T822 prep in,inactivation
R344 T824 T825 compound carrier,females
R345 T825 T823 pobj females,in
R346 T826 T817 aux have,demonstrated
R347 T827 T828 amod preferential,inactivation
R348 T828 T817 dobj inactivation,demonstrated
R349 T829 T828 prep of,inactivation
R350 T830 T831 det the,chromosome
R351 T831 T829 pobj chromosome,of
R352 T832 T831 acl bearing,chromosome
R353 T833 T834 det the,allele
R354 T834 T832 dobj allele,bearing
R355 T835 T834 amod abnormal,allele
R356 T836 T817 prep in,demonstrated
R357 T837 T838 det a,variety
R358 T838 T836 pobj variety,in
R359 T839 T838 prep of,variety
R360 T840 T839 pobj tissues,of
R361 T841 T842 punct [,2
R362 T842 T817 parataxis 2,demonstrated
R363 T843 T842 punct ],2
R364 T844 T817 punct ", ",demonstrated
R365 T845 T817 cc and,demonstrated
R366 T846 T847 det this,skewing
R367 T847 T848 nsubjpass skewing,thought
R368 T848 T817 conj thought,demonstrated
R369 T849 T847 prep of,skewing
R370 T850 T851 compound X,inactivation
R371 T851 T849 pobj inactivation,of
R372 T852 T851 punct -,inactivation
R373 T853 T848 auxpass is,thought
R374 T854 T855 aux to,explain
R375 T855 T848 xcomp explain,thought
R376 T856 T857 det the,phenotype
R377 T857 T855 dobj phenotype,explain
R378 T858 T857 amod mild,phenotype
R379 T859 T857 acl observed,phenotype
R380 T860 T859 prep in,observed
R381 T861 T860 pobj carriers,in
R382 T862 T848 punct .,thought