> top > docs > PMC:1584416 > spans > 2524-3183 > annotations

PMC:1584416 / 2524-3183 JSONTXT

Annnotations TAB JSON ListView MergeView

craft-sa-dev

Id Subject Object Predicate Lexical cue
T676 0-8 JJ denotes Compound
T677 9-22 NNS denotes heterozygotes
T678 23-26 VBP denotes are
T679 27-38 NNS denotes individuals
T680 39-47 VBG denotes carrying
T681 48-51 CD denotes two
T682 69-76 NNS denotes alleles
T683 52-61 JJ denotes different
T684 62-68 JJ denotes mutant
T685 77-79 IN denotes of
T686 80-83 DT denotes the
T687 89-93 NN denotes gene
T688 84-88 JJ denotes same
T689 93-94 . denotes .
T690 94-323 sentence denotes In the absence of a dominant (wild-type [wt]) allele, genetic interactions between recessive alleles (referred to here as “biallelic” effects) could result in different phenotypic outcomes including interallelic complementation.
T691 95-97 IN denotes In
T692 244-250 VB denotes result
T693 98-101 DT denotes the
T694 102-109 NN denotes absence
T695 110-112 IN denotes of
T696 113-114 DT denotes a
T697 141-147 NN denotes allele
T698 115-123 JJ denotes dominant
T699 124-125 -LRB- denotes (
T700 125-129 JJ denotes wild
T701 130-134 NN denotes type
T702 129-130 HYPH denotes -
T703 135-136 -LRB- denotes [
T704 136-138 NN denotes wt
T705 138-139 -RRB- denotes ]
T706 139-140 -RRB- denotes )
T707 147-149 , denotes ,
T708 149-156 JJ denotes genetic
T709 157-169 NNS denotes interactions
T710 170-177 IN denotes between
T711 178-187 JJ denotes recessive
T712 188-195 NNS denotes alleles
T713 196-197 -LRB- denotes (
T714 197-205 VBN denotes referred
T715 206-208 IN denotes to
T716 209-213 RB denotes here
T717 214-216 IN denotes as
T718 217-218 `` denotes “
T719 218-227 JJ denotes biallelic
T720 229-236 NNS denotes effects
T721 227-228 '' denotes ”
T722 236-237 -RRB- denotes )
T723 238-243 MD denotes could
T724 251-253 IN denotes in
T725 254-263 JJ denotes different
T726 275-283 NNS denotes outcomes
T727 264-274 JJ denotes phenotypic
T728 284-293 VBG denotes including
T729 294-306 JJ denotes interallelic
T730 307-322 NN denotes complementation
T731 322-323 . denotes .
T732 323-659 sentence denotes Although amelioration of disease symptoms by interallelic complementation would create an ascertainment bias in the clinic, the lack of evidence concerning interallelic complementation or other biallelic effects in human disease is likely caused by the difficulty in distinguishing such effects from environment and genetic background.
T733 324-332 IN denotes Although
T734 404-410 VB denotes create
T735 333-345 NN denotes amelioration
T736 346-348 IN denotes of
T737 349-356 NN denotes disease
T738 357-365 NNS denotes symptoms
T739 366-368 IN denotes by
T740 369-381 JJ denotes interallelic
T741 382-397 NN denotes complementation
T742 398-403 MD denotes would
T743 563-569 VBN denotes caused
T744 411-413 DT denotes an
T745 428-432 NN denotes bias
T746 414-427 NN denotes ascertainment
T747 433-435 IN denotes in
T748 436-439 DT denotes the
T749 440-446 NN denotes clinic
T750 446-448 , denotes ,
T751 448-451 DT denotes the
T752 452-456 NN denotes lack
T753 457-459 IN denotes of
T754 460-468 NN denotes evidence
T755 469-479 VBG denotes concerning
T756 480-492 JJ denotes interallelic
T757 493-508 NN denotes complementation
T758 509-511 CC denotes or
T759 512-517 JJ denotes other
T760 528-535 NNS denotes effects
T761 518-527 JJ denotes biallelic
T762 536-538 IN denotes in
T763 539-544 JJ denotes human
T764 545-552 NN denotes disease
T765 553-555 VBZ denotes is
T766 556-562 RB denotes likely
T767 570-572 IN denotes by
T768 573-576 DT denotes the
T769 577-587 NN denotes difficulty
T770 588-590 IN denotes in
T771 591-605 VBG denotes distinguishing
T772 606-610 JJ denotes such
T773 611-618 NNS denotes effects
T774 619-623 IN denotes from
T775 624-635 NN denotes environment
T776 636-639 CC denotes and
T777 640-647 JJ denotes genetic
T778 648-658 NN denotes background
T779 658-659 . denotes .
R351 T676 T677 amod Compound,heterozygotes
R352 T677 T678 nsubj heterozygotes,are
R353 T679 T678 attr individuals,are
R354 T680 T679 acl carrying,individuals
R355 T681 T682 nummod two,alleles
R356 T682 T680 dobj alleles,carrying
R357 T683 T682 amod different,alleles
R358 T684 T682 amod mutant,alleles
R359 T685 T682 prep of,alleles
R360 T686 T687 det the,gene
R362 T688 T687 amod same,gene
R363 T689 T678 punct .,are
R364 T691 T692 prep In,result
R365 T693 T694 det the,absence
R366 T694 T691 pobj absence,In
R367 T695 T694 prep of,absence
R368 T696 T697 det a,allele
R369 T697 T695 pobj allele,of
R370 T698 T697 amod dominant,allele
R371 T699 T697 punct (,allele
R372 T700 T701 amod wild,type
R373 T701 T697 nmod type,allele
R374 T702 T701 punct -,type
R375 T703 T701 punct [,type
R376 T704 T701 appos wt,type
R377 T705 T697 punct ],allele
R378 T706 T697 punct ),allele
R379 T707 T692 punct ", ",result
R380 T708 T709 amod genetic,interactions
R381 T709 T692 nsubj interactions,result
R382 T710 T709 prep between,interactions
R383 T711 T712 amod recessive,alleles
R384 T712 T710 pobj alleles,between
R385 T713 T709 punct (,interactions
R386 T714 T709 acl referred,interactions
R387 T715 T714 prep to,referred
R388 T716 T714 advmod here,referred
R389 T717 T714 prep as,referred
R390 T718 T717 punct “,as
R391 T719 T720 amod biallelic,effects
R393 T721 T720 punct ”,effects
R394 T722 T692 punct ),result
R395 T723 T692 aux could,result
R396 T724 T692 prep in,result
R397 T725 T726 amod different,outcomes
R399 T727 T726 amod phenotypic,outcomes
R400 T728 T726 prep including,outcomes
R401 T729 T730 amod interallelic,complementation
R402 T730 T728 pobj complementation,including
R403 T731 T692 punct .,result
R404 T733 T734 mark Although,create
R405 T734 T743 advcl create,caused
R406 T735 T734 nsubj amelioration,create
R407 T736 T735 prep of,amelioration
R408 T737 T738 compound disease,symptoms
R409 T738 T736 pobj symptoms,of
R410 T739 T735 prep by,amelioration
R411 T740 T741 amod interallelic,complementation
R412 T741 T739 pobj complementation,by
R413 T742 T734 aux would,create
R414 T744 T745 det an,bias
R416 T746 T745 compound ascertainment,bias
R417 T747 T734 prep in,create
R418 T748 T749 det the,clinic
R419 T749 T747 pobj clinic,in
R420 T750 T743 punct ", ",caused
R421 T751 T752 det the,lack
R422 T752 T743 nsubjpass lack,caused
R423 T753 T752 prep of,lack
R424 T754 T753 pobj evidence,of
R425 T755 T754 prep concerning,evidence
R426 T756 T757 amod interallelic,complementation
R427 T757 T755 pobj complementation,concerning
R428 T758 T757 cc or,complementation
R429 T759 T760 amod other,effects
R431 T761 T760 amod biallelic,effects
R432 T762 T757 prep in,complementation
R433 T763 T764 amod human,disease
R434 T764 T762 pobj disease,in
R435 T765 T743 auxpass is,caused
R436 T766 T743 advmod likely,caused
R437 T767 T743 agent by,caused
R438 T768 T769 det the,difficulty
R439 T769 T767 pobj difficulty,by
R440 T770 T769 prep in,difficulty
R441 T771 T770 pcomp distinguishing,in
R442 T772 T773 amod such,effects
R443 T773 T771 dobj effects,distinguishing
R444 T774 T771 prep from,distinguishing
R445 T775 T774 pobj environment,from
R446 T776 T775 cc and,environment
R447 T777 T778 amod genetic,background
R448 T778 T775 conj background,environment
R449 T779 T743 punct .,caused
R361 T687 T685 pobj gene,of
R392 T720 T717 pobj effects,as
R398 T726 T724 pobj outcomes,in
R415 T745 T734 dobj bias,create
R430 T760 T757 conj effects,complementation

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
T416 27-38 NCBITaxon:1 denotes individuals
T417 69-76 SO:0001023 denotes alleles
T418 89-93 SO:0000704 denotes gene
T419 141-147 SO:0001023 denotes allele
T420 149-156 SO:0000704 denotes genetic
T421 188-195 SO:0001023 denotes alleles
T422 220-227 SO:0001023 denotes allelic
T423 299-306 SO:0001023 denotes allelic
T424 374-381 SO:0001023 denotes allelic
T425 485-492 SO:0001023 denotes allelic
T426 520-527 SO:0001023 denotes allelic
T427 539-544 NCBITaxon:9606 denotes human
T428 640-647 SO:0000704 denotes genetic

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
T483 27-38 NCBITaxon:1 denotes individuals
T484 62-68 SO_EXT:sequence_altered_entity_or_alteration_process denotes mutant
T485 69-76 SO_EXT:0001023 denotes alleles
T486 89-93 SO_EXT:0000704 denotes gene
T487 125-134 SO_EXT:wild_type_entity_or_quality denotes wild-type
T488 136-138 SO_EXT:wild_type_entity_or_quality denotes wt
T489 141-147 SO_EXT:0001023 denotes allele
T490 149-156 SO_EXT:0000704 denotes genetic
T491 188-195 SO_EXT:0001023 denotes alleles
T492 220-227 SO_EXT:0001023 denotes allelic
T493 299-306 SO_EXT:0001023 denotes allelic
T494 374-381 SO_EXT:0001023 denotes allelic
T495 485-492 SO_EXT:0001023 denotes allelic
T496 520-527 SO_EXT:0001023 denotes allelic
T497 539-544 NCBITaxon:9606 denotes human
T498 640-647 SO_EXT:0000704 denotes genetic