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PMC:1382200 / 23720-24987 JSONTXT

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Id Subject Object Predicate Lexical cue
T14439 1266-1267 . denotes .
T14438 1252-1256 NN denotes cell
T14437 1257-1266 NNS denotes divisions
T14436 1249-1250 SYM denotes –
T14435 1250-1251 CD denotes 3
T14434 1248-1249 CD denotes 2
T14433 1240-1247 IN denotes through
T14432 1232-1239 NN denotes protein
T14431 1229-1231 CC denotes or
T14430 1228-1229 HYPH denotes /
T14429 1225-1228 CC denotes and
T14428 1220-1224 NN denotes mRNA
T14427 1211-1212 HYPH denotes -
T14426 1210-1211 NN denotes m
T14425 1201-1209 JJ denotes maternal
T14424 1212-1219 NN denotes calpain
T14423 1196-1200 DT denotes some
T14422 1193-1195 IN denotes of
T14421 1181-1192 NN denotes persistence
T14420 1177-1180 DT denotes the
T14419 1174-1176 IN denotes to
T14418 1170-1173 IN denotes due
T14417 1163-1169 RB denotes likely
T14416 1158-1162 RBS denotes most
T14415 1143-1144 HYPH denotes -
T14414 1144-1148 NN denotes cell
T14413 1142-1143 CD denotes 8
T14412 1149-1154 NN denotes stage
T14411 1138-1141 DT denotes the
T14410 1135-1137 IN denotes to
T14409 1125-1126 SYM denotes -
T14408 1124-1125 HYPH denotes /
T14407 1123-1124 SYM denotes -
T14406 1118-1123 NN denotes Capn2
T14405 1114-1117 JJ denotes few
T14404 1127-1134 NNS denotes embryos
T14403 1112-1113 DT denotes a
T14402 1109-1111 IN denotes of
T14401 1100-1108 NN denotes survival
T14400 1096-1099 DT denotes the
T14399 1094-1096 , denotes ,
T14398 1085-1094 NN denotes viability
T14397 1080-1084 NN denotes cell
T14396 1077-1079 IN denotes of
T14395 1070-1076 NN denotes aspect
T14394 1065-1069 DT denotes some
T14376 993-997 IN denotes into
T14375 988-992 VBZ denotes fits
T14374 973-978 NN denotes Capn2
T14373 979-987 NN denotes knockout
T14372 969-972 DT denotes The
T14371 968-1018 sentence denotes The Capn2 knockout fits into the latter category.
T14370 967-968 . denotes .
T14369 956-958 VB denotes be
T14368 952-955 RB denotes not
T14367 946-951 MD denotes could
T14366 959-967 VBN denotes isolated
T14365 937-939 NN denotes ES
T14364 930-936 NN denotes mutant
T14363 940-945 NNS denotes cells
T14362 919-929 JJ denotes homozygous
T14361 915-918 CC denotes and
T14360 901-905 RB denotes ever
T14359 897-900 VBP denotes are
T14358 884-888 JJ denotes null
T14357 880-883 JJ denotes few
T14356 878-879 DT denotes a
T14355 889-896 NNS denotes embryos
T14354 873-877 RB denotes only
T14353 871-873 , denotes ,
T14352 862-871 NNS denotes instances
T14351 856-861 DT denotes these
T14350 906-914 VBN denotes observed
T14349 853-855 IN denotes In
T14348 852-968 sentence denotes In these instances, only a few null embryos are ever observed and homozygous mutant ES cells could not be isolated.
T14347 851-852 . denotes .
T14346 850-851 -RRB- denotes ]
T14345 848-850 CD denotes 43
T14344 847-848 SYM denotes -
T14343 844-845 , denotes ,
T14342 843-844 CD denotes 3
T14341 845-847 CD denotes 39
T14340 842-843 -LRB- denotes [
T14339 829-834 JJ denotes early
T14338 835-841 NN denotes embryo
T14337 825-828 DT denotes the
T14336 822-824 IN denotes in
T14335 816-821 NNS denotes cells
T14334 813-815 IN denotes of
T14333 803-812 NN denotes viability
T14332 799-802 DT denotes the
T14331 791-798 RB denotes fatally
T14330 780-790 VB denotes compromise
T14329 777-779 TO denotes to
T14328 766-768 VBZ denotes is
T14327 750-754 NN denotes gene
T14326 755-765 NN denotes disruption
T14325 746-749 DT denotes the
T14324 744-746 , denotes ,
T14323 737-744 RB denotes however
T14322 735-737 , denotes ,
T14321 730-735 NNS denotes cases
T14320 724-729 JJ denotes other
T14319 769-776 VBN denotes thought
T14318 721-723 IN denotes In
T14317 720-852 sentence denotes In other cases, however, the gene disruption is thought to compromise fatally the viability of cells in the early embryo [3,39-43].
T14316 719-720 . denotes .
T14315 706-713 RB denotes usually
T14314 703-705 VBZ denotes is
T14313 693-702 NNS denotes genotypes
T14312 683-692 JJ denotes embryonic
T14311 680-682 IN denotes of
T14310 714-719 VBN denotes noted
T14309 657-666 JJ denotes Mendelian
T14308 667-679 NN denotes distribution
T14307 655-656 DT denotes a
T14306 651-654 CC denotes and
T14305 649-651 , denotes ,
T14304 637-643 NN denotes morula
T14303 644-649 NN denotes stage
T14302 633-636 DT denotes the
T14301 626-632 IN denotes beyond
T14300 612-617 RB denotes often
T14299 607-611 NN denotes type
T14298 602-606 DT denotes this
T14297 599-601 IN denotes of
T14296 618-625 VBP denotes survive
T14295 591-598 NNS denotes embryos
T14294 586-590 JJ denotes Null
T14293 585-720 sentence denotes Null embryos of this type often survive beyond the morula stage, and a Mendelian distribution of embryonic genotypes is usually noted.
T14292 584-585 . denotes .
T14291 583-584 -RRB- denotes ]
T14290 581-583 CD denotes 38
T14289 580-581 -LRB- denotes [
T14288 564-579 RB denotes morphologically
T14287 552-554 VB denotes be
T14286 546-551 RB denotes often
T14285 542-545 MD denotes can
T14284 555-563 VBN denotes observed
T14283 536-541 WDT denotes which
T14282 512-527 NN denotes differentiation
T14281 502-511 JJ denotes embryonic
T14280 528-535 NN denotes program
T14279 498-501 DT denotes the
T14278 495-497 IN denotes in
T14277 482-485 VBP denotes are
T14276 474-481 NNS denotes defects
T14275 472-474 , denotes ,
T14274 467-472 NNS denotes cases
T14273 462-466 DT denotes some
T14272 486-494 VBN denotes incurred
T14271 459-461 IN denotes In
T14270 458-585 sentence denotes In some cases, defects are incurred in the embryonic differentiation program which can often be observed morphologically [38].
T14269 457-458 . denotes .
T14268 443-450 JJ denotes general
T14267 451-457 NNS denotes causes
T14266 439-442 CD denotes two
T14265 436-438 IN denotes to
T14264 422-424 VB denotes be
T14263 412-421 RB denotes typically
T14262 408-411 MD denotes can
T14261 398-407 NNS denotes knockouts
T14260 393-397 NN denotes gene
T14259 388-392 IN denotes from
T14258 378-387 VBG denotes resulting
T14257 425-435 VBN denotes attributed
T14256 368-377 NN denotes lethality
T14255 352-367 NN denotes Preimplantation
T14254 351-458 sentence denotes Preimplantation lethality resulting from gene knockouts can typically be attributed to two general causes.
T14253 350-351 . denotes .
T14252 341-350 VBG denotes revealing
T14251 334-340 PRP denotes itself
T14250 331-333 IN denotes in
T14249 326-327 SYM denotes -
T14248 325-326 HYPH denotes /
T14247 324-325 SYM denotes -
T14246 319-324 NN denotes Capn2
T14245 316-318 VB denotes be
T14244 313-315 TO denotes to
T14243 281-297 JJ denotes pre-implantation
T14242 271-280 VBN denotes genotyped
T14241 258-270 RB denotes successfully
T14240 252-254 IN denotes of
T14239 248-251 IN denotes out
T14238 255-257 CD denotes 90
T14237 244-247 CD denotes two
T14236 298-305 NNS denotes embryos
T14235 239-243 RB denotes only
T14234 306-312 VBD denotes proved
T14233 234-238 IN denotes that
T14232 229-233 NN denotes fact
T14231 225-228 DT denotes the
T14230 223-225 , denotes ,
T14229 328-330 VBZ denotes is
T14228 216-223 RB denotes However
T14227 215-351 sentence denotes However, the fact that only two out of 90 successfully genotyped pre-implantation embryos proved to be Capn2-/- is in itself revealing.
T14226 214-215 . denotes .
T14225 193-206 JJ denotes morphological
T14224 185-192 JJ denotes obvious
T14223 207-214 NNS denotes defects
T14222 181-184 DT denotes any
T14221 169-172 RB denotes not
T14220 165-168 VBD denotes did
T14219 153-154 HYPH denotes -
T14218 154-158 NN denotes cell
T14217 152-153 CD denotes 8
T14216 159-164 NN denotes stage
T14215 148-151 DT denotes the
T14214 145-147 IN denotes at
T14213 134-144 VBN denotes identified
T14212 173-180 VB denotes present
T14211 121-125 JJ denotes null
T14210 110-120 JJ denotes homozygous
T14209 106-109 CD denotes two
T14208 126-133 NNS denotes embryos
T14207 102-105 DT denotes The
T14206 101-215 sentence denotes The two homozygous null embryos identified at the 8-cell stage did not present any obvious morphological defects.
T14205 100-101 . denotes .
T14204 86-90 VBN denotes been
T14203 82-85 RB denotes yet
T14202 78-81 RB denotes not
T14201 74-77 VBZ denotes has
T14200 64-65 SYM denotes -
T14199 63-64 HYPH denotes /
T14198 62-63 SYM denotes -
T14197 66-73 NNS denotes embryos
T14196 57-62 NN denotes Capn2
T14195 54-56 IN denotes in
T14194 28-43 NN denotes preimplantation
T14193 44-53 NN denotes lethality
T14192 24-27 DT denotes the
T14191 21-23 IN denotes of
T14190 91-100 VBN denotes clarified
T14189 4-14 VBG denotes underlying
T14188 15-20 NN denotes cause
T14187 0-3 DT denotes The
T14393 1061-1064 IN denotes for
T14392 1051-1060 JJ denotes essential
T14391 1039-1040 HYPH denotes -
T14390 1040-1047 NN denotes calpain
T14389 1038-1039 NN denotes m
T14388 1048-1050 VBZ denotes is
T14387 1033-1037 IN denotes that
T14386 1028-1032 JJ denotes true
T14385 1155-1157 VBZ denotes is
T14384 1022-1024 PRP denotes it
T14383 1025-1027 VBZ denotes is
T14382 1019-1021 IN denotes If
T14381 1018-1267 sentence denotes If it is true that m-calpain is essential for some aspect of cell viability, the survival of a few Capn2-/- embryos to the 8-cell stage is most likely due to the persistence of some maternal m-calpain mRNA and/or protein through 2–3 cell divisions.
T14380 1017-1018 . denotes .
T14379 1002-1008 JJ denotes latter
T14378 1009-1017 NN denotes category
T14377 998-1001 DT denotes the
R3606 T14187 T14188 det The,cause
R3608 T14188 T14190 nsubjpass cause,clarified
R3609 T14189 T14188 amod underlying,cause
R3611 T14191 T14188 prep of,cause
R3612 T14192 T14193 det the,lethality
R3613 T14193 T14191 pobj lethality,of
R3615 T14194 T14193 compound preimplantation,lethality
R3616 T14195 T14188 prep in,cause
R3617 T14196 T14197 nmod Capn2,embryos
R3619 T14197 T14195 pobj embryos,in
R3620 T14198 T14196 punct -,Capn2
R3622 T14199 T14196 punct /,Capn2
R3623 T14200 T14196 punct -,Capn2
R3624 T14201 T14190 aux has,clarified
R3626 T14202 T14190 neg not,clarified
R3627 T14203 T14190 advmod yet,clarified
R3628 T14204 T14190 auxpass been,clarified
R3630 T14205 T14190 punct .,clarified
R3632 T14207 T14208 det The,embryos
R3633 T14208 T14212 nsubj embryos,present
R3634 T14209 T14208 nummod two,embryos
R3636 T14210 T14211 amod homozygous,null
R3637 T14211 T14208 amod null,embryos
R3639 T14213 T14208 acl identified,embryos
R3640 T14214 T14213 prep at,identified
R3641 T14215 T14216 det the,stage
R3643 T14216 T14214 pobj stage,at
R3644 T14217 T14218 nummod 8,cell
R3645 T14218 T14216 compound cell,stage
R3647 T14219 T14218 punct -,cell
R3648 T14220 T14212 aux did,present
R3649 T14221 T14212 neg not,present
R3651 T14222 T14223 det any,defects
R3652 T14223 T14212 dobj defects,present
R3654 T14224 T14223 amod obvious,defects
R3655 T14225 T14223 amod morphological,defects
R3656 T14226 T14212 punct .,present
R3657 T14228 T14229 advmod However,is
R3659 T14230 T14229 punct ", ",is
R3660 T14231 T14232 det the,fact
R3661 T14232 T14229 nsubj fact,is
R3663 T14233 T14234 mark that,proved
R3664 T14234 T14232 acl proved,fact
R3665 T14235 T14236 advmod only,embryos
R3667 T14236 T14234 nsubj embryos,proved
R3668 T14237 T14238 quantmod two,90
R3669 T14238 T14236 nummod 90,embryos
R3671 T14239 T14238 quantmod out,90
R3672 T14240 T14238 quantmod of,90
R3673 T14241 T14242 advmod successfully,genotyped
R3675 T14242 T14236 amod genotyped,embryos
R3676 T14243 T14236 amod pre-implantation,embryos
R3677 T14244 T14245 aux to,be
R3679 T14245 T14234 xcomp be,proved
R3680 T14246 T14245 attr Capn2,be
R3681 T14247 T14246 punct -,Capn2
R3683 T14248 T14246 punct /,Capn2
R3684 T14249 T14246 punct -,Capn2
R3686 T14250 T14229 prep in,is
R3687 T14251 T14250 pobj itself,in
R3688 T14252 T14229 acomp revealing,is
R3692 T14253 T14229 punct .,is
R3694 T14255 T14256 compound Preimplantation,lethality
R3695 T14256 T14257 nsubjpass lethality,attributed
R3697 T14258 T14256 acl resulting,lethality
R3698 T14259 T14258 prep from,resulting
R3700 T14260 T14261 compound gene,knockouts
R3701 T14261 T14259 pobj knockouts,from
R3703 T14262 T14257 aux can,attributed
R3704 T14263 T14257 advmod typically,attributed
R3705 T14264 T14257 auxpass be,attributed
R3706 T14265 T14257 prep to,attributed
R3707 T14266 T14267 nummod two,causes
R3708 T14267 T14265 pobj causes,to
R3710 T14268 T14267 amod general,causes
R3711 T14269 T14257 punct .,attributed
R3713 T14271 T14272 prep In,incurred
R3714 T14273 T14274 det some,cases
R3716 T14274 T14271 pobj cases,In
R3717 T14275 T14272 punct ", ",incurred
R3719 T14276 T14272 nsubjpass defects,incurred
R3720 T14277 T14272 auxpass are,incurred
R3721 T14278 T14272 prep in,incurred
R3724 T14279 T14280 det the,program
R3726 T14280 T14278 pobj program,in
R3727 T14281 T14280 amod embryonic,program
R3728 T14282 T14280 compound differentiation,program
R3730 T14283 T14284 dep which,observed
R3731 T14284 T14280 relcl observed,program
R3732 T14285 T14284 aux can,observed
R3734 T14286 T14284 advmod often,observed
R3735 T14287 T14284 auxpass be,observed
R3737 T14288 T14284 advmod morphologically,observed
R3738 T14289 T14290 punct [,38
R3740 T14290 T14284 parataxis 38,observed
R3741 T14291 T14290 punct ],38
R3742 T14292 T14272 punct .,incurred
R3744 T14294 T14295 amod Null,embryos
R3745 T14295 T14296 nsubj embryos,survive
R3747 T14297 T14295 prep of,embryos
R3748 T14298 T14299 det this,type
R3750 T14299 T14297 pobj type,of
R3751 T14300 T14296 advmod often,survive
R3753 T14301 T14296 prep beyond,survive
R3754 T14302 T14303 det the,stage
R3755 T14303 T14301 pobj stage,beyond
R3757 T14304 T14303 compound morula,stage
R3758 T14305 T14296 punct ", ",survive
R3759 T14306 T14296 cc and,survive
R3760 T14307 T14308 det a,distribution
R3761 T14308 T14310 nsubjpass distribution,noted
R3763 T14309 T14308 amod Mendelian,distribution
R3764 T14310 T14296 conj noted,survive
R3765 T14311 T14308 prep of,distribution
R3767 T14312 T14313 amod embryonic,genotypes
R3768 T14313 T14311 pobj genotypes,of
R3769 T14314 T14310 auxpass is,noted
R3770 T14315 T14310 advmod usually,noted
R3772 T14316 T14310 punct .,noted
R3773 T14318 T14319 prep In,thought
R3775 T14320 T14321 amod other,cases
R3776 T14321 T14318 pobj cases,In
R3777 T14322 T14319 punct ", ",thought
R3779 T14323 T14319 advmod however,thought
R3780 T14324 T14319 punct ", ",thought
R3782 T14325 T14326 det the,disruption
R3783 T14326 T14319 nsubjpass disruption,thought
R3784 T14327 T14326 compound gene,disruption
R3786 T14328 T14319 auxpass is,thought
R3787 T14329 T14330 aux to,compromise
R3789 T14330 T14319 xcomp compromise,thought
R3790 T14331 T14330 advmod fatally,compromise
R3791 T14332 T14333 det the,viability
R3792 T14359 T14350 auxpass are,observed
R3793 T14333 T14330 dobj viability,compromise
R3794 T14334 T14333 prep of,viability
R3795 T14335 T14334 pobj cells,of
R3796 T14336 T14335 prep in,cells
R3797 T14360 T14350 advmod ever,observed
R3798 T14337 T14338 det the,embryo
R3799 T14338 T14336 pobj embryo,in
R3800 T14339 T14338 amod early,embryo
R3801 T14361 T14350 cc and,observed
R3802 T14340 T14341 punct [,39
R3803 T14341 T14330 parataxis 39,compromise
R3804 T14342 T14341 dep 3,39
R3805 T14362 T14363 amod homozygous,cells
R3806 T14343 T14341 punct ",",39
R3807 T14344 T14345 punct -,43
R3808 T14345 T14341 prep 43,39
R3809 T14363 T14366 nsubjpass cells,isolated
R3810 T14346 T14341 punct ],39
R3811 T14347 T14319 punct .,thought
R3812 T14349 T14350 prep In,observed
R3813 T14364 T14363 compound mutant,cells
R3814 T14351 T14352 det these,instances
R3815 T14352 T14349 pobj instances,In
R3816 T14353 T14350 punct ", ",observed
R3817 T14365 T14363 compound ES,cells
R3818 T14354 T14355 advmod only,embryos
R3819 T14355 T14350 nsubjpass embryos,observed
R3820 T14356 T14355 det a,embryos
R3821 T14366 T14350 conj isolated,observed
R3822 T14357 T14355 amod few,embryos
R3823 T14358 T14355 amod null,embryos
R3824 T14367 T14366 aux could,isolated
R3825 T14368 T14366 neg not,isolated
R3826 T14369 T14366 auxpass be,isolated
R3827 T14370 T14366 punct .,isolated
R3828 T14372 T14373 det The,knockout
R3830 T14373 T14375 nsubj knockout,fits
R3834 T14374 T14373 compound Capn2,knockout
R3837 T14376 T14375 prep into,fits
R3842 T14377 T14378 det the,category
R3846 T14378 T14376 pobj category,into
R3850 T14379 T14378 amod latter,category
R3853 T14380 T14375 punct .,fits
R3857 T14382 T14383 mark If,is
R3865 T14383 T14385 advcl is,is
R3869 T14384 T14383 nsubj it,is
R3871 T14386 T14383 acomp true,is
R3875 T14387 T14388 mark that,is
R3879 T14388 T14383 ccomp is,is
R3883 T14389 T14390 compound m,calpain
R3886 T14390 T14388 nsubj calpain,is
R3890 T14391 T14390 punct -,calpain
R3894 T14392 T14388 acomp essential,is
R3896 T14393 T14392 prep for,essential
R3900 T14394 T14395 det some,aspect
R3903 T14395 T14393 pobj aspect,for
R3905 T14396 T14395 prep of,aspect
R3908 T14397 T14398 compound cell,viability
R3912 T14398 T14396 pobj viability,of
R3920 T14399 T14385 punct ", ",is
R3923 T14400 T14401 det the,survival
R3924 T14401 T14385 nsubj survival,is
R3928 T14402 T14401 prep of,survival
R3931 T14403 T14404 det a,embryos
R3934 T14404 T14402 pobj embryos,of
R3937 T14405 T14404 amod few,embryos
R3941 T14406 T14404 nmod Capn2,embryos
R3944 T14407 T14406 punct -,Capn2
R3947 T14408 T14406 punct /,Capn2
R3951 T14409 T14406 punct -,Capn2
R3954 T14410 T14401 prep to,survival
R3958 T14411 T14412 det the,stage
R3962 T14412 T14410 pobj stage,to
R3967 T14413 T14414 nummod 8,cell
R3968 T14414 T14412 compound cell,stage
R3972 T14415 T14414 punct -,cell
R3974 T14416 T14417 advmod most,likely
R3977 T14417 T14418 advmod likely,due
R3981 T14418 T14385 prep due,is
R3985 T14419 T14418 pcomp to,due
R3988 T14420 T14421 det the,persistence
R3992 T14421 T14418 pobj persistence,due
R3996 T14422 T14421 prep of,persistence
R4000 T14423 T14424 det some,calpain
R4004 T14424 T14422 pobj calpain,of
R4008 T14425 T14424 amod maternal,calpain
R4011 T14426 T14424 compound m,calpain
R4014 T14427 T14424 punct -,calpain
R4016 T14428 T14424 appos mRNA,calpain
R4022 T14429 T14428 cc and,mRNA
R4026 T14430 T14429 punct /,and
R4029 T14431 T14429 cc or,and
R4033 T14432 T14428 conj protein,mRNA
R4037 T14433 T14421 prep through,persistence
R4038 T14434 T14435 quantmod 2,3
R4040 T14435 T14437 nummod 3,divisions
R4042 T14436 T14435 punct –,3
R4046 T14437 T14433 pobj divisions,through
R4049 T14438 T14437 compound cell,divisions
R4053 T14439 T14385 punct .,is

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
T12338 1252-1266 GO:0051301 denotes cell divisions
T12337 1142-1154 UBERON:0019252 denotes 8-cell stage
T12336 1127-1134 UBERON:0000922 denotes embryos
T12335 1118-1123 PR:000005015 denotes Capn2
T12334 973-978 PR:000005015 denotes Capn2
T12333 937-945 CL:0002322 denotes ES cells
T12332 889-896 UBERON:0000922 denotes embryos
T12331 829-841 UBERON:0019248 denotes early embryo
T12330 750-754 SO:0000704 denotes gene
T12329 683-692 UBERON:0000922 denotes embryonic
T12328 637-643 UBERON:0000085 denotes morula
T12327 591-598 UBERON:0000922 denotes embryos
T12326 502-511 UBERON:0000922 denotes embryonic
T12325 393-397 SO:0000704 denotes gene
T12324 355-367 GO:0007566 denotes implantation
T12323 319-324 PR:000005015 denotes Capn2
T12322 298-305 UBERON:0000922 denotes embryos
T12321 285-297 GO:0007566 denotes implantation
T12320 152-164 UBERON:0019252 denotes 8-cell stage
T12319 126-133 UBERON:0000922 denotes embryos
T12318 66-73 UBERON:0000922 denotes embryos
T12317 57-62 PR:000005015 denotes Capn2
T12316 31-43 GO:0007566 denotes implantation

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
T12673 1252-1266 GO:0051301 denotes cell divisions
T12672 1252-1256 CL_GO_EXT:cell denotes cell
T12671 1232-1239 CHEBI_PR_EXT:protein denotes protein
T12670 1220-1224 CHEBI_SO_EXT:mRNA denotes mRNA
T12669 1210-1219 GO_PR_EXT:calpain_2_complex denotes m-calpain
T12668 1144-1148 CL_GO_EXT:cell denotes cell
T12667 1142-1154 UBERON:0019252 denotes 8-cell stage
T12666 1127-1134 UBERON:0000922 denotes embryos
T12665 1125-1126 SO_EXT:sequence_nullness_or_absence denotes -
T12664 1123-1124 SO_EXT:sequence_nullness_or_absence denotes -
T12663 1118-1123 PR_EXT:000005015 denotes Capn2
T12662 1080-1084 CL_GO_EXT:cell denotes cell
T12661 1038-1047 GO_PR_EXT:calpain_2_complex denotes m-calpain
T12660 973-978 PR_EXT:000005015 denotes Capn2
T12659 940-945 CL_GO_EXT:cell denotes cells
T12658 937-945 CL:0002322 denotes ES cells
T12657 930-936 SO_EXT:sequence_altered_entity_or_alteration_process denotes mutant
T12656 889-896 UBERON:0000922 denotes embryos
T12655 884-888 SO_EXT:sequence_nullness denotes null
T12654 829-841 UBERON:0019248 denotes early embryo
T12653 816-821 CL_GO_EXT:cell denotes cells
T12652 791-798 GO_EXT:fatality_or_lethality denotes fatally
T12651 750-754 SO_EXT:0000704 denotes gene
T12650 693-702 SO_EXT:genotype_or_entity_with_genotype denotes genotypes
T12649 683-692 UBERON:0000922 denotes embryonic
T12648 637-643 UBERON:0000085 denotes morula
T12647 591-598 UBERON:0000922 denotes embryos
T12646 586-590 SO_EXT:sequence_nullness denotes Null
T12645 512-527 GO_RO_EXT:developmental_differentiation_process denotes differentiation
T12644 502-511 UBERON:0000922 denotes embryonic
T12643 393-397 SO_EXT:0000704 denotes gene
T12642 368-377 GO_EXT:fatality_or_lethality denotes lethality
T12641 355-367 GO:0007566 denotes implantation
T12640 326-327 SO_EXT:sequence_nullness_or_absence denotes -
T12639 324-325 SO_EXT:sequence_nullness_or_absence denotes -
T12638 319-324 PR_EXT:000005015 denotes Capn2
T12637 298-305 UBERON:0000922 denotes embryos
T12636 285-297 GO:0007566 denotes implantation
T12635 154-158 CL_GO_EXT:cell denotes cell
T12634 152-164 UBERON:0019252 denotes 8-cell stage
T12633 126-133 UBERON:0000922 denotes embryos
T12632 121-125 SO_EXT:sequence_nullness denotes null
T12631 66-73 UBERON:0000922 denotes embryos
T12630 64-65 SO_EXT:sequence_nullness_or_absence denotes -
T12629 62-63 SO_EXT:sequence_nullness_or_absence denotes -
T12628 57-62 PR_EXT:000005015 denotes Capn2
T12627 44-53 GO_EXT:fatality_or_lethality denotes lethality
T12626 31-43 GO:0007566 denotes implantation