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PMC:1584416 / 24817-25364 JSONTXT 4 Projects

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Id Subject Object Predicate Lexical cue
T4339 0-3 DT denotes The
T4341 4-12 VBN denotes observed
T4342 13-22 JJ denotes biallelic
T4340 23-30 NNS denotes effects
T4343 31-35 VBD denotes were
T4344 36-38 IN denotes of
T4345 39-44 CD denotes three
T4347 45-52 JJ denotes general
T4346 53-58 NNS denotes types
T4348 58-59 . denotes .
T4349 59-247 sentence denotes In the first, the allele associated in a homozygous state with a phenotype closer to wt singularly determined the phenotypic outcome, a phenomenon widely known in human recessive disease.
T4350 60-62 IN denotes In
T4352 63-66 DT denotes the
T4353 67-72 JJ denotes first
T4354 72-74 , denotes ,
T4355 74-77 DT denotes the
T4356 78-84 NN denotes allele
T4357 85-95 VBN denotes associated
T4358 96-98 IN denotes in
T4359 99-100 DT denotes a
T4361 101-111 JJ denotes homozygous
T4360 112-117 NN denotes state
T4362 118-122 IN denotes with
T4363 123-124 DT denotes a
T4364 125-134 NN denotes phenotype
T4365 135-141 RBR denotes closer
T4366 142-144 IN denotes to
T4367 145-147 NN denotes wt
T4368 148-158 RB denotes singularly
T4351 159-169 VBN denotes determined
T4369 170-173 DT denotes the
T4371 174-184 JJ denotes phenotypic
T4370 185-192 NN denotes outcome
T4372 192-194 , denotes ,
T4373 194-195 DT denotes a
T4374 196-206 NN denotes phenomenon
T4375 207-213 RB denotes widely
T4376 214-219 VBN denotes known
T4377 220-222 IN denotes in
T4378 223-228 JJ denotes human
T4380 229-238 JJ denotes recessive
T4379 239-246 NN denotes disease
T4381 246-247 . denotes .
T4382 247-378 sentence denotes Because these Xpd alleles functioned at or near wt levels with respect to a particular function, we call these effects “dominant”.
T4383 248-255 IN denotes Because
T4385 256-261 DT denotes these
T4387 262-265 NN denotes Xpd
T4386 266-273 NNS denotes alleles
T4384 274-284 VBD denotes functioned
T4389 285-287 IN denotes at
T4390 288-290 CC denotes or
T4391 291-295 IN denotes near
T4392 296-298 NN denotes wt
T4393 299-305 NNS denotes levels
T4394 306-310 IN denotes with
T4395 311-318 NN denotes respect
T4396 319-321 IN denotes to
T4397 322-323 DT denotes a
T4399 324-334 JJ denotes particular
T4398 335-343 NN denotes function
T4400 343-345 , denotes ,
T4401 345-347 PRP denotes we
T4388 348-352 VBP denotes call
T4402 353-358 DT denotes these
T4403 359-366 NNS denotes effects
T4404 367-368 `` denotes “
T4405 368-376 JJ denotes dominant
T4406 376-377 '' denotes ”
T4407 377-378 . denotes .
T4408 378-547 sentence denotes Such alleles can also be referred to as “separation of function” alleles, because they allow dissection of the roles of multifunctional proteins in specific phenotypes.
T4409 379-383 JJ denotes Such
T4410 384-391 NNS denotes alleles
T4412 392-395 MD denotes can
T4413 396-400 RB denotes also
T4414 401-403 VB denotes be
T4411 404-412 VBN denotes referred
T4415 413-415 IN denotes to
T4416 416-418 IN denotes as
T4417 419-420 `` denotes “
T4419 420-430 NN denotes separation
T4420 431-433 IN denotes of
T4421 434-442 NN denotes function
T4422 442-443 '' denotes ”
T4418 444-451 NNS denotes alleles
T4423 451-453 , denotes ,
T4424 453-460 IN denotes because
T4426 461-465 PRP denotes they
T4425 466-471 VBP denotes allow
T4427 472-482 NN denotes dissection
T4428 483-485 IN denotes of
T4429 486-489 DT denotes the
T4430 490-495 NNS denotes roles
T4431 496-498 IN denotes of
T4432 499-514 JJ denotes multifunctional
T4433 515-523 NN denotes proteins
T4434 524-526 IN denotes in
T4435 527-535 JJ denotes specific
T4436 536-546 NNS denotes phenotypes
T4437 546-547 . denotes .
R2951 T4339 T4340 det The,effects
R2952 T4340 T4343 nsubj effects,were
R2953 T4341 T4340 amod observed,effects
R2954 T4342 T4340 amod biallelic,effects
R2955 T4344 T4343 prep of,were
R2956 T4345 T4346 nummod three,types
R2957 T4346 T4344 pobj types,of
R2958 T4347 T4346 amod general,types
R2959 T4348 T4343 punct .,were
R2960 T4350 T4351 prep In,determined
R2961 T4352 T4353 det the,first
R2962 T4353 T4350 pobj first,In
R2963 T4354 T4351 punct ", ",determined
R2964 T4355 T4356 det the,allele
R2965 T4356 T4351 nsubj allele,determined
R2966 T4357 T4356 acl associated,allele
R2967 T4358 T4357 prep in,associated
R2968 T4359 T4360 det a,state
R2969 T4360 T4358 pobj state,in
R2970 T4361 T4360 amod homozygous,state
R2971 T4362 T4357 prep with,associated
R2972 T4363 T4364 det a,phenotype
R2973 T4364 T4362 pobj phenotype,with
R2974 T4365 T4366 advmod closer,to
R2975 T4366 T4364 amod to,phenotype
R2976 T4367 T4366 pobj wt,to
R2977 T4368 T4351 advmod singularly,determined
R2978 T4369 T4370 det the,outcome
R2979 T4370 T4351 dobj outcome,determined
R2980 T4371 T4370 amod phenotypic,outcome
R2981 T4372 T4351 punct ", ",determined
R2982 T4373 T4374 det a,phenomenon
R2983 T4374 T4351 npadvmod phenomenon,determined
R2984 T4375 T4376 advmod widely,known
R2985 T4376 T4374 acl known,phenomenon
R2986 T4377 T4376 prep in,known
R2987 T4378 T4379 amod human,disease
R2988 T4379 T4377 pobj disease,in
R2989 T4380 T4379 amod recessive,disease
R2990 T4381 T4351 punct .,determined
R2991 T4383 T4384 mark Because,functioned
R2992 T4384 T4388 advcl functioned,call
R2993 T4385 T4386 det these,alleles
R2994 T4386 T4384 nsubj alleles,functioned
R2995 T4387 T4386 compound Xpd,alleles
R2996 T4389 T4384 prep at,functioned
R2997 T4390 T4389 cc or,at
R2998 T4391 T4389 conj near,at
R2999 T4392 T4393 compound wt,levels
R3000 T4393 T4391 pobj levels,near
R3001 T4394 T4384 prep with,functioned
R3002 T4395 T4394 pobj respect,with
R3003 T4396 T4395 prep to,respect
R3004 T4397 T4398 det a,function
R3005 T4398 T4396 pobj function,to
R3006 T4399 T4398 amod particular,function
R3007 T4400 T4388 punct ", ",call
R3008 T4401 T4388 nsubj we,call
R3009 T4402 T4403 det these,effects
R3010 T4403 T4388 dobj effects,call
R3011 T4404 T4388 punct “,call
R3012 T4405 T4388 oprd dominant,call
R3013 T4406 T4388 punct ”,call
R3014 T4407 T4388 punct .,call
R3015 T4409 T4410 amod Such,alleles
R3016 T4410 T4411 nsubjpass alleles,referred
R3017 T4412 T4411 aux can,referred
R3018 T4413 T4411 advmod also,referred
R3019 T4414 T4411 auxpass be,referred
R3020 T4415 T4411 prep to,referred
R3021 T4416 T4411 prep as,referred
R3022 T4417 T4418 punct “,alleles
R3023 T4418 T4416 pobj alleles,as
R3024 T4419 T4418 nmod separation,alleles
R3025 T4420 T4419 prep of,separation
R3026 T4421 T4420 pobj function,of
R3027 T4422 T4418 punct ”,alleles
R3028 T4423 T4411 punct ", ",referred
R3029 T4424 T4425 mark because,allow
R3030 T4425 T4411 advcl allow,referred
R3031 T4426 T4425 nsubj they,allow
R3032 T4427 T4425 dobj dissection,allow
R3033 T4428 T4427 prep of,dissection
R3034 T4429 T4430 det the,roles
R3035 T4430 T4428 pobj roles,of
R3036 T4431 T4430 prep of,roles
R3037 T4432 T4433 amod multifunctional,proteins
R3038 T4433 T4431 pobj proteins,of
R3039 T4434 T4425 prep in,allow
R3040 T4435 T4436 amod specific,phenotypes
R3041 T4436 T4434 pobj phenotypes,in
R3042 T4437 T4411 punct .,referred