craft-sa-dev Home  

PMC:314463 / 20324-21131 JSONTXT 5 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue
T4618 0-2 IN denotes As
T4620 3-4 DT denotes a
T4622 5-12 JJ denotes visible
T4621 13-19 NN denotes marker
T4623 19-21 , denotes ,
T4624 21-26 JJ denotes early
T4626 27-34 NN denotes linkage
T4625 35-42 NNS denotes studies
T4627 43-47 IN denotes with
T4628 48-51 DT denotes the
T4630 52-60 JJ denotes original
T4631 61-67 JJ denotes droopy
T4632 68-71 NN denotes ear
T4629 72-78 NN denotes allele
T4633 79-81 CC denotes or
T4634 82-85 DT denotes the
T4636 86-89 NN denotes deH
T4635 90-96 NN denotes allele
T4619 97-107 VBD denotes identified
T4637 108-109 DT denotes a
T4639 110-113 NN denotes map
T4638 114-122 NN denotes position
T4640 123-125 IN denotes in
T4641 126-129 DT denotes the
T4642 130-136 NN denotes middle
T4643 137-139 IN denotes of
T4644 140-150 NN denotes Chromosome
T4645 151-152 CD denotes 3
T4646 152-154 , denotes ,
T4647 154-160 JJ denotes distal
T4648 161-163 IN denotes to
T4649 164-170 JJ denotes matted
T4650 171-174 CC denotes and
T4651 175-183 JJ denotes proximal
T4652 184-186 IN denotes to
T4653 187-195 NNP denotes Varitint
T4655 195-196 HYPH denotes -
T4654 196-203 NNP denotes waddler
T4656 204-205 -LRB- denotes (
T4657 205-211 NNP denotes Carter
T4658 212-215 CC denotes and
T4659 216-224 NNP denotes Falconer
T4660 225-229 CD denotes 1951
T4661 229-230 : denotes ;
T4662 231-236 NNP denotes Curry
T4663 237-241 CD denotes 1959
T4664 241-242 : denotes ;
T4665 243-247 NNP denotes Lane
T4666 248-251 CC denotes and
T4667 252-258 NNP denotes Eicher
T4668 259-263 CD denotes 1979
T4669 263-264 : denotes ;
T4670 265-271 NNP denotes Holmes
T4671 272-274 FW denotes et
T4672 275-278 FW denotes al.
T4673 279-283 CD denotes 1981
T4674 283-284 -RRB- denotes )
T4675 284-285 . denotes .
T4676 285-584 sentence denotes We used an F2 intercross with CAST/Ei mice to localize deH to a 0.1 cM interval between D3Mit213 and 16.MMHAP32FLF1, which was refined by development of a bacterial artificial chromosome (BAC) contig and additional markers to a 1.4 Mb region that contained eight genes, including Tbx15 (Figure 3A).
T4677 286-288 PRP denotes We
T4678 289-293 VBD denotes used
T4679 294-296 DT denotes an
T4681 297-299 NN denotes F2
T4680 300-310 NN denotes intercross
T4682 311-315 IN denotes with
T4683 316-320 NN denotes CAST
T4685 320-321 HYPH denotes /
T4684 321-323 NN denotes Ei
T4686 324-328 NNS denotes mice
T4687 329-331 TO denotes to
T4688 332-340 VB denotes localize
T4689 341-344 NN denotes deH
T4690 345-347 IN denotes to
T4691 348-349 DT denotes a
T4693 350-353 CD denotes 0.1
T4694 354-356 NN denotes cM
T4692 357-365 NN denotes interval
T4695 366-373 IN denotes between
T4696 374-382 NN denotes D3Mit213
T4697 383-386 CC denotes and
T4698 387-401 NN denotes 16.MMHAP32FLF1
T4699 401-403 , denotes ,
T4700 403-408 WDT denotes which
T4702 409-412 VBD denotes was
T4701 413-420 VBN denotes refined
T4703 421-423 IN denotes by
T4704 424-435 NN denotes development
T4705 436-438 IN denotes of
T4706 439-440 DT denotes a
T4708 441-450 JJ denotes bacterial
T4710 451-461 JJ denotes artificial
T4709 462-472 NN denotes chromosome
T4711 473-474 -LRB- denotes (
T4712 474-477 NN denotes BAC
T4713 477-478 -RRB- denotes )
T4707 479-485 NN denotes contig
T4714 486-489 CC denotes and
T4715 490-500 JJ denotes additional
T4716 501-508 NNS denotes markers
T4717 509-511 IN denotes to
T4718 512-513 DT denotes a
T4720 514-517 CD denotes 1.4
T4721 518-520 NN denotes Mb
T4719 521-527 NN denotes region
T4722 528-532 WDT denotes that
T4723 533-542 VBD denotes contained
T4724 543-548 CD denotes eight
T4725 549-554 NNS denotes genes
T4726 554-556 , denotes ,
T4727 556-565 VBG denotes including
T4728 566-571 NN denotes Tbx15
T4729 572-573 -LRB- denotes (
T4730 573-579 NN denotes Figure
T4731 580-582 CD denotes 3A
T4732 582-583 -RRB- denotes )
T4733 583-584 . denotes .
T4734 584-807 sentence denotes We considered Tbx15 as an excellent candidate for the skeletal abnormalities caused by deH, based on studies by Agulnik et al. (1998), who described its embryonic expression in the craniofacial region and developing limbs.
T4735 585-587 PRP denotes We
T4736 588-598 VBD denotes considered
T4737 599-604 NN denotes Tbx15
T4738 605-607 IN denotes as
T4739 608-610 DT denotes an
T4741 611-620 JJ denotes excellent
T4740 621-630 NN denotes candidate
T4742 631-634 IN denotes for
T4743 635-638 DT denotes the
T4745 639-647 JJ denotes skeletal
T4744 648-661 NNS denotes abnormalities
T4746 662-668 VBN denotes caused
T4747 669-671 IN denotes by
T4748 672-675 NN denotes deH
T4749 675-677 , denotes ,
T4750 677-682 VBN denotes based
T4751 683-685 IN denotes on
T4752 686-693 NNS denotes studies
T4753 694-696 IN denotes by
T4754 697-704 NNP denotes Agulnik
T4755 705-707 FW denotes et
T4756 708-711 FW denotes al.
T4757 712-713 -LRB- denotes (
T4758 713-717 CD denotes 1998
T4759 717-718 -RRB- denotes )
T4760 718-720 , denotes ,
T4761 720-723 WP denotes who
T4762 724-733 VBD denotes described
T4763 734-737 PRP$ denotes its
T4765 738-747 JJ denotes embryonic
T4764 748-758 NN denotes expression
T4766 759-761 IN denotes in
T4767 762-765 DT denotes the
T4769 766-778 JJ denotes craniofacial
T4768 779-785 NN denotes region
T4770 786-789 CC denotes and
T4771 790-800 VBG denotes developing
T4772 801-806 NNS denotes limbs
T4773 806-807 . denotes .
R3091 T4618 T4619 prep As,identified
R3092 T4620 T4621 det a,marker
R3093 T4621 T4618 pobj marker,As
R3094 T4622 T4621 amod visible,marker
R3095 T4623 T4619 punct ", ",identified
R3096 T4624 T4625 amod early,studies
R3097 T4625 T4619 nsubj studies,identified
R3098 T4626 T4625 compound linkage,studies
R3099 T4627 T4625 prep with,studies
R3100 T4628 T4629 det the,allele
R3101 T4629 T4627 pobj allele,with
R3102 T4630 T4629 amod original,allele
R3103 T4631 T4632 amod droopy,ear
R3104 T4632 T4629 compound ear,allele
R3105 T4633 T4629 cc or,allele
R3106 T4634 T4635 det the,allele
R3107 T4635 T4629 conj allele,allele
R3108 T4636 T4635 compound deH,allele
R3109 T4637 T4638 det a,position
R3110 T4638 T4619 dobj position,identified
R3111 T4639 T4638 compound map,position
R3112 T4640 T4638 prep in,position
R3113 T4641 T4642 det the,middle
R3114 T4642 T4640 pobj middle,in
R3115 T4643 T4642 prep of,middle
R3116 T4644 T4643 pobj Chromosome,of
R3117 T4645 T4644 nummod 3,Chromosome
R3118 T4646 T4638 punct ", ",position
R3119 T4647 T4638 amod distal,position
R3120 T4648 T4647 prep to,distal
R3121 T4649 T4648 amod matted,to
R3122 T4650 T4647 cc and,distal
R3123 T4651 T4647 conj proximal,distal
R3124 T4652 T4651 prep to,proximal
R3125 T4653 T4654 compound Varitint,waddler
R3126 T4654 T4652 pobj waddler,to
R3127 T4655 T4654 punct -,waddler
R3128 T4656 T4657 punct (,Carter
R3129 T4657 T4619 meta Carter,identified
R3130 T4658 T4657 cc and,Carter
R3131 T4659 T4657 conj Falconer,Carter
R3132 T4660 T4659 nummod 1951,Falconer
R3133 T4661 T4659 punct ;,Falconer
R3134 T4662 T4659 conj Curry,Falconer
R3135 T4663 T4662 nummod 1959,Curry
R3136 T4664 T4662 punct ;,Curry
R3137 T4665 T4662 conj Lane,Curry
R3138 T4666 T4665 cc and,Lane
R3139 T4667 T4665 conj Eicher,Lane
R3140 T4668 T4667 nummod 1979,Eicher
R3141 T4669 T4667 punct ;,Eicher
R3142 T4670 T4667 conj Holmes,Eicher
R3143 T4671 T4670 nmod et,Holmes
R3144 T4672 T4670 nmod al.,Holmes
R3145 T4673 T4670 nummod 1981,Holmes
R3146 T4674 T4670 punct ),Holmes
R3147 T4675 T4619 punct .,identified
R3148 T4677 T4678 nsubj We,used
R3149 T4679 T4680 det an,intercross
R3150 T4680 T4678 dobj intercross,used
R3151 T4681 T4680 compound F2,intercross
R3152 T4682 T4680 prep with,intercross
R3153 T4683 T4684 compound CAST,Ei
R3154 T4684 T4686 compound Ei,mice
R3155 T4685 T4684 punct /,Ei
R3156 T4686 T4682 pobj mice,with
R3157 T4687 T4688 aux to,localize
R3158 T4688 T4678 advcl localize,used
R3159 T4689 T4688 dobj deH,localize
R3160 T4690 T4688 prep to,localize
R3161 T4691 T4692 det a,interval
R3162 T4692 T4690 pobj interval,to
R3163 T4693 T4694 nummod 0.1,cM
R3164 T4694 T4692 compound cM,interval
R3165 T4695 T4692 prep between,interval
R3166 T4696 T4695 pobj D3Mit213,between
R3167 T4697 T4696 cc and,D3Mit213
R3168 T4698 T4696 conj 16.MMHAP32FLF1,D3Mit213
R3169 T4699 T4692 punct ", ",interval
R3170 T4700 T4701 dep which,refined
R3171 T4701 T4692 relcl refined,interval
R3172 T4702 T4701 auxpass was,refined
R3173 T4703 T4701 prep by,refined
R3174 T4704 T4703 pobj development,by
R3175 T4705 T4704 prep of,development
R3176 T4706 T4707 det a,contig
R3177 T4707 T4705 pobj contig,of
R3178 T4708 T4709 amod bacterial,chromosome
R3179 T4709 T4707 nmod chromosome,contig
R3180 T4710 T4709 amod artificial,chromosome
R3181 T4711 T4709 punct (,chromosome
R3182 T4712 T4709 appos BAC,chromosome
R3183 T4713 T4707 punct ),contig
R3184 T4714 T4707 cc and,contig
R3185 T4715 T4716 amod additional,markers
R3186 T4716 T4707 conj markers,contig
R3187 T4717 T4716 prep to,markers
R3188 T4718 T4719 det a,region
R3189 T4719 T4717 pobj region,to
R3190 T4720 T4721 nummod 1.4,Mb
R3191 T4721 T4719 compound Mb,region
R3192 T4722 T4723 dep that,contained
R3193 T4723 T4719 relcl contained,region
R3194 T4724 T4725 nummod eight,genes
R3195 T4725 T4723 dobj genes,contained
R3196 T4726 T4725 punct ", ",genes
R3197 T4727 T4725 prep including,genes
R3198 T4728 T4727 pobj Tbx15,including
R3199 T4729 T4730 punct (,Figure
R3200 T4730 T4688 parataxis Figure,localize
R3201 T4731 T4730 nummod 3A,Figure
R3202 T4732 T4730 punct ),Figure
R3203 T4733 T4678 punct .,used
R3204 T4735 T4736 nsubj We,considered
R3205 T4737 T4736 dobj Tbx15,considered
R3206 T4738 T4736 prep as,considered
R3207 T4739 T4740 det an,candidate
R3208 T4740 T4738 pobj candidate,as
R3209 T4741 T4740 amod excellent,candidate
R3210 T4742 T4740 prep for,candidate
R3211 T4743 T4744 det the,abnormalities
R3212 T4744 T4742 pobj abnormalities,for
R3213 T4745 T4744 amod skeletal,abnormalities
R3214 T4746 T4744 acl caused,abnormalities
R3215 T4747 T4746 agent by,caused
R3216 T4748 T4747 pobj deH,by
R3217 T4749 T4736 punct ", ",considered
R3218 T4750 T4736 prep based,considered
R3219 T4751 T4750 prep on,based
R3220 T4752 T4751 pobj studies,on
R3221 T4753 T4752 prep by,studies
R3222 T4754 T4753 pobj Agulnik,by
R3223 T4755 T4756 advmod et,al.
R3224 T4756 T4754 advmod al.,Agulnik
R3225 T4757 T4754 punct (,Agulnik
R3226 T4758 T4754 npadvmod 1998,Agulnik
R3227 T4759 T4754 punct ),Agulnik
R3228 T4760 T4754 punct ", ",Agulnik
R3229 T4761 T4762 dep who,described
R3230 T4762 T4754 relcl described,Agulnik
R3231 T4763 T4764 poss its,expression
R3232 T4764 T4762 dobj expression,described
R3233 T4765 T4764 amod embryonic,expression
R3234 T4766 T4764 prep in,expression
R3235 T4767 T4768 det the,region
R3236 T4768 T4766 pobj region,in
R3237 T4769 T4768 amod craniofacial,region
R3238 T4770 T4768 cc and,region
R3239 T4771 T4772 amod developing,limbs
R3240 T4772 T4768 conj limbs,region
R3241 T4773 T4736 punct .,considered