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PMC:1440874 / 155-1506 JSONTXT

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craft-sa-dev

Id Subject Object Predicate Lexical cue
T226 294-296 IN denotes of
T170 0-149 sentence denotes ATRX is an X-encoded member of the SNF2 family of ATPase/helicase proteins thought to regulate gene expression by modifying chromatin at target loci.
T171 0-4 NN denotes ATRX
T172 5-7 VBZ denotes is
T173 8-10 DT denotes an
T174 21-27 NN denotes member
T175 11-12 NN denotes X
T176 12-13 HYPH denotes -
T177 13-20 VBN denotes encoded
T178 28-30 IN denotes of
T179 31-34 DT denotes the
T180 40-46 NN denotes family
T181 35-39 NN denotes SNF2
T182 47-49 IN denotes of
T183 50-56 NN denotes ATPase
T184 57-65 NN denotes helicase
T185 56-57 HYPH denotes /
T186 66-74 NN denotes proteins
T187 75-82 VBN denotes thought
T188 83-85 TO denotes to
T189 86-94 VB denotes regulate
T190 95-99 NN denotes gene
T191 100-110 NN denotes expression
T192 111-113 IN denotes by
T193 114-123 VBG denotes modifying
T194 124-133 NN denotes chromatin
T195 134-136 IN denotes at
T196 137-143 NN denotes target
T197 144-148 NNS denotes loci
T198 148-149 . denotes .
T199 149-263 sentence denotes Mutations in ATRX provided the first example of a human genetic disease associated with defects in such proteins.
T200 150-159 NNS denotes Mutations
T201 168-176 VBD denotes provided
T202 160-162 IN denotes in
T203 163-167 NN denotes ATRX
T204 177-180 DT denotes the
T205 187-194 NN denotes example
T206 181-186 JJ denotes first
T207 195-197 IN denotes of
T208 198-199 DT denotes a
T209 214-221 NN denotes disease
T210 200-205 JJ denotes human
T211 206-213 JJ denotes genetic
T212 222-232 VBN denotes associated
T213 233-237 IN denotes with
T214 238-245 NNS denotes defects
T215 246-248 IN denotes in
T216 249-253 JJ denotes such
T217 254-262 NN denotes proteins
T218 262-263 . denotes .
T219 263-520 sentence denotes To better understand the role of ATRX in development and the associated abnormalities in the ATR-X (alpha thalassemia mental retardation, X-linked) syndrome, we conditionally inactivated the homolog in mice, Atrx, at the 8- to 16-cell stage of development.
T220 264-266 TO denotes To
T221 274-284 VB denotes understand
T222 267-273 RBR denotes better
T223 439-450 VBD denotes inactivated
T224 285-288 DT denotes the
T225 289-293 NN denotes role
T227 297-301 NN denotes ATRX
T228 302-304 IN denotes in
T229 305-316 NN denotes development
T230 317-320 CC denotes and
T231 321-324 DT denotes the
T232 336-349 NNS denotes abnormalities
T233 325-335 VBN denotes associated
T234 350-352 IN denotes in
T235 353-356 DT denotes the
T236 412-420 NN denotes syndrome
T237 357-360 NN denotes ATR
T238 361-362 NN denotes X
T239 360-361 HYPH denotes -
T240 363-364 -LRB- denotes (
T241 364-369 NN denotes alpha
T242 370-381 NN denotes thalassemia
T243 382-388 JJ denotes mental
T244 389-400 NN denotes retardation
T245 400-402 , denotes ,
T246 402-403 NN denotes X
T247 404-410 VBN denotes linked
T248 403-404 HYPH denotes -
T249 410-411 -RRB- denotes )
T250 420-422 , denotes ,
T251 422-424 PRP denotes we
T252 425-438 RB denotes conditionally
T253 451-454 DT denotes the
T254 455-462 NN denotes homolog
T255 463-465 IN denotes in
T256 466-470 NNS denotes mice
T257 470-472 , denotes ,
T258 472-476 NN denotes Atrx
T259 476-478 , denotes ,
T260 478-480 IN denotes at
T261 481-484 DT denotes the
T262 499-504 NN denotes stage
T263 485-486 CD denotes 8
T264 491-493 CD denotes 16
T265 486-487 HYPH denotes -
T266 488-490 IN denotes to
T267 494-498 NN denotes cell
T268 493-494 HYPH denotes -
T269 505-507 IN denotes of
T270 508-519 NN denotes development
T271 519-520 . denotes .
T272 520-822 sentence denotes The protein, Atrx, was ubiquitously expressed, and male embryos null for Atrx implanted and gastrulated normally but did not survive beyond 9.5 days postcoitus due to a defect in formation of the extraembryonic trophoblast, one of the first terminally differentiated lineages in the developing embryo.
T273 521-524 DT denotes The
T274 525-532 NN denotes protein
T275 557-566 VBN denotes expressed
T276 532-534 , denotes ,
T277 534-538 NN denotes Atrx
T278 538-540 , denotes ,
T279 540-543 VBD denotes was
T280 544-556 RB denotes ubiquitously
T281 566-568 , denotes ,
T282 568-571 CC denotes and
T283 572-576 JJ denotes male
T284 577-584 NNS denotes embryos
T285 599-608 VBN denotes implanted
T286 585-589 JJ denotes null
T287 590-593 IN denotes for
T288 594-598 NN denotes Atrx
T289 609-612 CC denotes and
T290 613-624 VBN denotes gastrulated
T291 625-633 RB denotes normally
T292 634-637 CC denotes but
T293 638-641 VBD denotes did
T294 646-653 VB denotes survive
T295 642-645 RB denotes not
T296 654-660 IN denotes beyond
T297 661-664 CD denotes 9.5
T298 665-669 NNS denotes days
T299 670-680 RB denotes postcoitus
T300 681-684 IN denotes due
T301 685-687 IN denotes to
T302 688-689 DT denotes a
T303 690-696 NN denotes defect
T304 697-699 IN denotes in
T305 700-709 NN denotes formation
T306 710-712 IN denotes of
T307 713-716 DT denotes the
T308 732-743 NN denotes trophoblast
T309 717-731 JJ denotes extraembryonic
T310 743-745 , denotes ,
T311 745-748 CD denotes one
T312 749-751 IN denotes of
T313 752-755 DT denotes the
T314 788-796 NNS denotes lineages
T315 756-761 JJ denotes first
T316 762-772 RB denotes terminally
T317 773-787 VBN denotes differentiated
T318 797-799 IN denotes in
T319 800-803 DT denotes the
T320 815-821 NN denotes embryo
T321 804-814 VBG denotes developing
T322 821-822 . denotes .
T323 822-981 sentence denotes Carrier female mice that inherit a maternal null allele should be affected, since the paternal X chromosome is normally inactivated in extraembryonic tissues.
T324 823-830 NN denotes Carrier
T325 838-842 NNS denotes mice
T326 831-837 JJ denotes female
T327 889-897 VBN denotes affected
T328 843-847 WDT denotes that
T329 848-855 VBP denotes inherit
T330 856-857 DT denotes a
T331 872-878 NN denotes allele
T332 858-866 JJ denotes maternal
T333 867-871 JJ denotes null
T334 879-885 MD denotes should
T335 886-888 VB denotes be
T336 897-899 , denotes ,
T337 899-904 IN denotes since
T338 931-933 VBZ denotes is
T339 905-908 DT denotes the
T340 920-930 NN denotes chromosome
T341 909-917 JJ denotes paternal
T342 918-919 NN denotes X
T343 934-942 RB denotes normally
T344 943-954 JJ denotes inactivated
T345 955-957 IN denotes in
T346 958-972 JJ denotes extraembryonic
T347 973-980 NNS denotes tissues
T348 980-981 . denotes .
T349 981-1142 sentence denotes Surprisingly, however, some carrier females established a normal placenta and appeared to escape the usual pattern of imprinted X-inactivation in these tissues.
T350 982-994 RB denotes Surprisingly
T351 1026-1037 VBD denotes established
T352 994-996 , denotes ,
T353 996-1003 RB denotes however
T354 1003-1005 , denotes ,
T355 1005-1009 DT denotes some
T356 1018-1025 NNS denotes females
T357 1010-1017 NN denotes carrier
T358 1038-1039 DT denotes a
T359 1047-1055 NN denotes placenta
T360 1040-1046 JJ denotes normal
T361 1056-1059 CC denotes and
T362 1060-1068 VBD denotes appeared
T363 1069-1071 TO denotes to
T364 1072-1078 VB denotes escape
T365 1079-1082 DT denotes the
T366 1089-1096 NN denotes pattern
T367 1083-1088 JJ denotes usual
T368 1097-1099 IN denotes of
T369 1100-1109 VBN denotes imprinted
T370 1112-1124 NN denotes inactivation
T371 1110-1111 NN denotes X
T372 1111-1112 HYPH denotes -
T373 1125-1127 IN denotes in
T374 1128-1133 DT denotes these
T375 1134-1141 NNS denotes tissues
T376 1141-1142 . denotes .
T377 1142-1351 sentence denotes Together these findings demonstrate an unexpected, specific, and essential role for Atrx in the development of the murine trophoblast and present an example of escape from imprinted X chromosome inactivation.
T378 1143-1151 RB denotes Together
T379 1167-1178 VBP denotes demonstrate
T380 1152-1157 DT denotes these
T381 1158-1166 NNS denotes findings
T382 1179-1181 DT denotes an
T383 1218-1222 NN denotes role
T384 1182-1192 JJ denotes unexpected
T385 1192-1194 , denotes ,
T386 1194-1202 JJ denotes specific
T387 1202-1204 , denotes ,
T388 1204-1207 CC denotes and
T389 1208-1217 JJ denotes essential
T390 1223-1226 IN denotes for
T391 1227-1231 NN denotes Atrx
T392 1232-1234 IN denotes in
T393 1235-1238 DT denotes the
T394 1239-1250 NN denotes development
T395 1251-1253 IN denotes of
T396 1254-1257 DT denotes the
T397 1265-1276 NN denotes trophoblast
T398 1258-1264 JJ denotes murine
T399 1277-1280 CC denotes and
T400 1281-1288 VBP denotes present
T401 1289-1291 DT denotes an
T402 1292-1299 NN denotes example
T403 1300-1302 IN denotes of
T404 1303-1309 NN denotes escape
T405 1310-1314 IN denotes from
T406 1315-1324 VBN denotes imprinted
T407 1327-1337 NN denotes chromosome
T408 1325-1326 NN denotes X
T409 1338-1350 NN denotes inactivation
T410 1350-1351 . denotes .
R15 T171 T172 nsubj ATRX,is
R16 T173 T174 det an,member
R17 T174 T172 attr member,is
R21 T178 T174 prep of,member
R22 T179 T180 det the,family
R23 T180 T178 pobj family,of
R25 T182 T180 prep of,family
R26 T183 T184 compound ATPase,helicase
R27 T184 T186 compound helicase,proteins
R29 T186 T182 pobj proteins,of
R30 T187 T174 acl thought,member
R31 T188 T189 aux to,regulate
R32 T189 T187 xcomp regulate,thought
R33 T190 T191 compound gene,expression
R34 T191 T189 dobj expression,regulate
R35 T192 T189 prep by,regulate
R36 T193 T192 pcomp modifying,by
R37 T194 T193 dobj chromatin,modifying
R38 T195 T193 prep at,modifying
R39 T196 T197 compound target,loci
R40 T197 T195 pobj loci,at
R41 T198 T172 punct .,is
R42 T200 T201 nsubj Mutations,provided
R43 T202 T200 prep in,Mutations
R44 T203 T202 pobj ATRX,in
R45 T204 T205 det the,example
R46 T205 T201 dobj example,provided
R48 T207 T205 prep of,example
R49 T208 T209 det a,disease
R50 T209 T207 pobj disease,of
R53 T212 T209 acl associated,disease
R54 T213 T212 prep with,associated
R55 T214 T213 pobj defects,with
R56 T215 T214 prep in,defects
R57 T216 T217 amod such,proteins
R58 T217 T215 pobj proteins,in
R59 T218 T201 punct .,provided
R60 T220 T221 aux To,understand
R61 T221 T223 advcl understand,inactivated
R63 T224 T225 det the,role
R64 T225 T221 dobj role,understand
R65 T226 T225 prep of,role
R66 T227 T226 pobj ATRX,of
R67 T228 T225 prep in,role
R68 T229 T228 pobj development,in
R69 T230 T225 cc and,role
R70 T231 T232 det the,abnormalities
R71 T232 T225 conj abnormalities,role
R73 T234 T232 prep in,abnormalities
R74 T235 T236 det the,syndrome
R75 T236 T234 pobj syndrome,in
R77 T238 T236 nmod X,syndrome
R78 T239 T238 punct -,X
R86 T247 T242 amod linked,thalassemia
R87 T248 T247 punct -,linked
R89 T250 T223 punct ", ",inactivated
R90 T251 T223 nsubj we,inactivated
R91 T252 T223 advmod conditionally,inactivated
R92 T253 T254 det the,homolog
R93 T254 T223 dobj homolog,inactivated
R94 T255 T254 prep in,homolog
R95 T256 T255 pobj mice,in
R96 T257 T254 punct ", ",homolog
R97 T258 T254 appos Atrx,homolog
R98 T259 T223 punct ", ",inactivated
R99 T260 T223 prep at,inactivated
R100 T261 T262 det the,stage
R101 T262 T260 pobj stage,at
R103 T264 T267 nummod 16,cell
R104 T265 T264 punct -,16
R105 T266 T264 quantmod to,16
R106 T267 T262 compound cell,stage
R107 T268 T267 punct -,cell
R108 T269 T262 prep of,stage
R109 T270 T269 pobj development,of
R110 T271 T223 punct .,inactivated
R111 T273 T274 det The,protein
R112 T274 T275 nsubjpass protein,expressed
R113 T276 T274 punct ", ",protein
R114 T277 T274 appos Atrx,protein
R115 T278 T275 punct ", ",expressed
R116 T279 T275 auxpass was,expressed
R117 T280 T275 advmod ubiquitously,expressed
R118 T281 T275 punct ", ",expressed
R119 T282 T275 cc and,expressed
R120 T283 T284 amod male,embryos
R121 T284 T285 nsubj embryos,implanted
R122 T285 T275 conj implanted,expressed
R126 T289 T285 cc and,implanted
R127 T290 T285 conj gastrulated,implanted
R128 T291 T285 advmod normally,implanted
R129 T292 T285 cc but,implanted
R130 T293 T294 aux did,survive
R131 T294 T285 conj survive,implanted
R133 T296 T294 prep beyond,survive
R134 T297 T298 nummod 9.5,days
R135 T298 T296 pobj days,beyond
R136 T299 T298 advmod postcoitus,days
R137 T300 T294 prep due,survive
R138 T301 T300 pcomp to,due
R139 T302 T303 det a,defect
R140 T303 T300 pobj defect,due
R141 T304 T303 prep in,defect
R142 T305 T304 pobj formation,in
R143 T306 T305 prep of,formation
R144 T307 T308 det the,trophoblast
R145 T308 T306 pobj trophoblast,of
R147 T310 T308 punct ", ",trophoblast
R148 T311 T308 appos one,trophoblast
R149 T312 T311 prep of,one
R150 T313 T314 det the,lineages
R151 T314 T312 pobj lineages,of
R155 T318 T314 prep in,lineages
R156 T319 T320 det the,embryo
R157 T320 T318 pobj embryo,in
R159 T322 T285 punct .,implanted
R160 T324 T325 nmod Carrier,mice
R161 T325 T327 nsubjpass mice,affected
R163 T328 T329 dep that,inherit
R164 T329 T325 relcl inherit,mice
R165 T330 T331 det a,allele
R166 T331 T329 dobj allele,inherit
R169 T334 T327 aux should,affected
R170 T335 T327 auxpass be,affected
R171 T336 T327 punct ", ",affected
R172 T337 T338 mark since,is
R173 T338 T327 advcl is,affected
R175 T340 T338 nsubj chromosome,is
R176 T341 T340 amod paternal,chromosome
R177 T342 T340 compound X,chromosome
R178 T343 T338 advmod normally,is
R179 T344 T338 acomp inactivated,is
R180 T345 T338 prep in,is
R181 T346 T347 amod extraembryonic,tissues
R182 T347 T345 pobj tissues,in
R183 T348 T327 punct .,affected
R184 T350 T351 advmod Surprisingly,established
R185 T352 T351 punct ", ",established
R186 T353 T351 advmod however,established
R187 T354 T351 punct ", ",established
R188 T355 T356 det some,females
R189 T356 T351 nsubj females,established
R191 T358 T359 det a,placenta
R192 T359 T351 dobj placenta,established
R194 T361 T351 cc and,established
R195 T362 T351 conj appeared,established
R196 T363 T364 aux to,escape
R197 T364 T362 xcomp escape,appeared
R198 T365 T366 det the,pattern
R199 T366 T364 dobj pattern,escape
R201 T368 T366 prep of,pattern
R202 T369 T370 amod imprinted,inactivation
R203 T370 T368 pobj inactivation,of
R206 T373 T364 prep in,escape
R207 T374 T375 det these,tissues
R208 T375 T373 pobj tissues,in
R209 T376 T351 punct .,established
R210 T378 T379 advmod Together,demonstrate
R211 T380 T381 det these,findings
R212 T381 T379 nsubj findings,demonstrate
R213 T382 T383 det an,role
R214 T383 T379 dobj role,demonstrate
R221 T390 T383 prep for,role
R222 T391 T390 pobj Atrx,for
R223 T392 T383 prep in,role
R224 T393 T394 det the,development
R225 T394 T392 pobj development,in
R226 T395 T394 prep of,development
R227 T396 T397 det the,trophoblast
R228 T397 T395 pobj trophoblast,of
R230 T399 T379 cc and,demonstrate
R231 T400 T379 conj present,demonstrate
R232 T401 T402 det an,example
R233 T402 T400 dobj example,present
R234 T403 T402 prep of,example
R235 T404 T403 pobj escape,of
R236 T405 T404 prep from,escape
R237 T406 T407 amod imprinted,chromosome
R238 T407 T409 compound chromosome,inactivation
R240 T409 T405 pobj inactivation,from
R241 T410 T379 punct .,demonstrate
R18 T175 T174 nmod X,member
R19 T176 T175 punct -,X
R20 T177 T175 amod encoded,X
R24 T181 T180 compound SNF2,family
R28 T185 T184 punct /,helicase
R47 T206 T205 amod first,example
R51 T210 T209 amod human,disease
R52 T211 T209 amod genetic,disease
R62 T222 T221 advmod better,understand
R72 T233 T232 amod associated,abnormalities
R76 T237 T238 nmod ATR,X
R79 T240 T238 punct (,X
R80 T241 T242 compound alpha,thalassemia
R81 T242 T238 appos thalassemia,X
R82 T243 T244 amod mental,retardation
R83 T244 T242 appos retardation,thalassemia
R84 T245 T242 punct ", ",thalassemia
R85 T246 T247 npadvmod X,linked
R88 T249 T236 punct ),syndrome
R102 T263 T264 quantmod 8,16
R123 T286 T284 amod null,embryos
R124 T287 T286 prep for,null
R125 T288 T287 pobj Atrx,for
R132 T295 T294 neg not,survive
R146 T309 T308 amod extraembryonic,trophoblast
R152 T315 T314 amod first,lineages
R153 T316 T317 advmod terminally,differentiated
R154 T317 T314 amod differentiated,lineages
R158 T321 T320 amod developing,embryo
R162 T326 T325 amod female,mice
R167 T332 T331 amod maternal,allele
R168 T333 T331 amod null,allele
R174 T339 T340 det the,chromosome
R190 T357 T356 compound carrier,females
R193 T360 T359 amod normal,placenta
R200 T367 T366 amod usual,pattern
R204 T371 T370 compound X,inactivation
R205 T372 T370 punct -,inactivation
R215 T384 T383 amod unexpected,role
R216 T385 T384 punct ", ",unexpected
R217 T386 T384 conj specific,unexpected
R218 T387 T386 punct ", ",specific
R219 T388 T386 cc and,specific
R220 T389 T386 conj essential,specific
R229 T398 T397 amod murine,trophoblast
R239 T408 T407 compound X,chromosome

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
T97 0-4 PR_EXT:000004503 denotes ATRX
T98 11-12 GO:0000805 denotes X
T99 13-20 SO_EXT:sequence_coding_function denotes encoded
T100 35-39 PR_EXT:P22082 denotes SNF2
T101 50-56 GO_EXT:0016887 denotes ATPase
T102 57-65 GO_EXT:0004386 denotes helicase
T103 66-74 CHEBI_PR_EXT:protein denotes proteins
T104 86-94 GO:0065007 denotes regulate
T105 95-99 SO_EXT:0000704 denotes gene
T106 95-110 GO:0010467 denotes gene expression
T107 124-133 GO:0000785 denotes chromatin
T108 150-159 SO_EXT:sequence_alteration_entity_or_process denotes Mutations
T109 163-167 PR_EXT:000004503 denotes ATRX
T110 200-205 NCBITaxon:9606 denotes human
T111 206-213 SO_EXT:0000704 denotes genetic
T112 254-262 CHEBI_PR_EXT:protein denotes proteins
T113 297-301 PR_EXT:000004503 denotes ATRX
T114 361-362 GO:0000805 denotes X
T115 402-403 GO:0000805 denotes X
T116 455-462 SO_EXT:0000853 denotes homolog
T117 466-470 NCBITaxon:10088 denotes mice
T118 472-476 PR_EXT:000004503 denotes Atrx
T119 494-498 CL_GO_EXT:cell denotes cell
T120 525-532 CHEBI_PR_EXT:protein denotes protein
T121 534-538 PR_EXT:000004503 denotes Atrx
T122 557-566 GO:0010467 denotes expressed
T123 572-576 PATO_UBERON_EXT:male_or_bearer_of_maleness denotes male
T124 577-584 UBERON:0000922 denotes embryos
T125 585-589 SO_EXT:sequence_nullness denotes null
T126 594-598 PR_EXT:000004503 denotes Atrx
T127 599-608 GO:0007566 denotes implanted
T128 613-624 GO:0007369 denotes gastrulated
T129 674-680 GO:0007620 denotes coitus
T130 722-731 UBERON:0000922 denotes embryonic
T131 732-743 UBERON:0000088 denotes trophoblast
T132 773-787 GO_PATO_RO_EXT:developmental_differentiation_process_or_quality denotes differentiated
T133 815-821 UBERON:0000922 denotes embryo
T134 831-837 PATO_UBERON_EXT:female_or_bearer_of_femaleness denotes female
T135 838-842 NCBITaxon:10088 denotes mice
T136 867-871 SO_EXT:sequence_nullness denotes null
T137 872-878 SO_EXT:0001023 denotes allele
T138 918-930 GO:0000805 denotes X chromosome
T139 920-930 GO_SO_EXT:chromosome denotes chromosome
T140 958-980 UBERON:0005292 denotes extraembryonic tissues
T141 1018-1025 PATO_UBERON_EXT:female_or_bearer_of_femaleness denotes females
T142 1047-1055 UBERON:0001987 denotes placenta
T143 1100-1124 GO:0060819 denotes imprinted X-inactivation
T144 1110-1111 GO:0000805 denotes X
T145 1134-1141 UBERON:0000479 denotes tissues
T146 1227-1231 PR_EXT:000004503 denotes Atrx
T147 1258-1264 NCBITaxon:39107 denotes murine
T148 1265-1276 UBERON:0000088 denotes trophoblast
T149 1315-1350 GO:0060819 denotes imprinted X chromosome inactivation
T150 1325-1337 GO:0000805 denotes X chromosome
T151 1327-1337 GO_SO_EXT:chromosome denotes chromosome

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
T53 0-4 PR:000004503 denotes ATRX
T54 11-12 GO:0000805 denotes X
T55 35-39 PR:P22082 denotes SNF2
T56 86-94 GO:0065007 denotes regulate
T57 95-99 SO:0000704 denotes gene
T58 95-110 GO:0010467 denotes gene expression
T59 124-133 GO:0000785 denotes chromatin
T60 163-167 PR:000004503 denotes ATRX
T61 200-205 NCBITaxon:9606 denotes human
T62 206-213 SO:0000704 denotes genetic
T63 297-301 PR:000004503 denotes ATRX
T64 361-362 GO:0000805 denotes X
T65 402-403 GO:0000805 denotes X
T66 455-462 SO:0000853 denotes homolog
T67 466-470 NCBITaxon:10088 denotes mice
T68 472-476 PR:000004503 denotes Atrx
T69 534-538 PR:000004503 denotes Atrx
T70 557-566 GO:0010467 denotes expressed
T71 577-584 UBERON:0000922 denotes embryos
T72 594-598 PR:000004503 denotes Atrx
T73 599-608 GO:0007566 denotes implanted
T74 613-624 GO:0007369 denotes gastrulated
T75 674-680 GO:0007620 denotes coitus
T76 722-731 UBERON:0000922 denotes embryonic
T77 732-743 UBERON:0000088 denotes trophoblast
T78 815-821 UBERON:0000922 denotes embryo
T79 838-842 NCBITaxon:10088 denotes mice
T80 872-878 SO:0001023 denotes allele
T81 918-930 GO:0000805 denotes X chromosome
T82 958-980 UBERON:0005292 denotes extraembryonic tissues
T83 1047-1055 UBERON:0001987 denotes placenta
T84 1100-1124 GO:0060819 denotes imprinted X-inactivation
T85 1110-1111 GO:0000805 denotes X
T86 1134-1141 UBERON:0000479 denotes tissues
T87 1227-1231 PR:000004503 denotes Atrx
T88 1258-1264 NCBITaxon:39107 denotes murine
T89 1265-1276 UBERON:0000088 denotes trophoblast
T90 1315-1350 GO:0060819 denotes imprinted X chromosome inactivation
T91 1325-1337 GO:0000805 denotes X chromosome