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PMC:1440874 / 0-1866 JSONTXT

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craft-sa-dev

Id Subject Object Predicate Lexical cue
T226 449-451 IN denotes of
T152 0-4 NN denotes Loss
T153 13-20 VBZ denotes Affects
T154 0-104 sentence denotes Loss of Atrx Affects Trophoblast Development and the Pattern of X-Inactivation in Extraembryonic Tissues
T155 5-7 IN denotes of
T156 8-12 NN denotes Atrx
T157 21-32 NN denotes Trophoblast
T158 33-44 NN denotes Development
T159 45-48 CC denotes and
T161 53-60 NN denotes Pattern
T162 61-63 IN denotes of
T163 64-65 NN denotes X
T164 66-78 NN denotes Inactivation
T165 65-66 HYPH denotes -
T166 79-81 IN denotes in
T167 82-96 JJ denotes Extraembryonic
T168 97-104 NNS denotes Tissues
T169 104-105 sentence denotes
T170 155-304 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 155-159 NN denotes ATRX
T172 160-162 VBZ denotes is
T173 163-165 DT denotes an
T174 176-182 NN denotes member
T175 166-167 NN denotes X
T176 167-168 HYPH denotes -
T177 168-175 VBN denotes encoded
T178 183-185 IN denotes of
T179 186-189 DT denotes the
T180 195-201 NN denotes family
T181 190-194 NN denotes SNF2
T182 202-204 IN denotes of
T183 205-211 NN denotes ATPase
T184 212-220 NN denotes helicase
T185 211-212 HYPH denotes /
T186 221-229 NN denotes proteins
T187 230-237 VBN denotes thought
T188 238-240 TO denotes to
T189 241-249 VB denotes regulate
T190 250-254 NN denotes gene
T191 255-265 NN denotes expression
T192 266-268 IN denotes by
T193 269-278 VBG denotes modifying
T194 279-288 NN denotes chromatin
T195 289-291 IN denotes at
T196 292-298 NN denotes target
T197 299-303 NNS denotes loci
T198 303-304 . denotes .
T199 304-418 sentence denotes Mutations in ATRX provided the first example of a human genetic disease associated with defects in such proteins.
T200 305-314 NNS denotes Mutations
T201 323-331 VBD denotes provided
T202 315-317 IN denotes in
T203 318-322 NN denotes ATRX
T204 332-335 DT denotes the
T205 342-349 NN denotes example
T206 336-341 JJ denotes first
T207 350-352 IN denotes of
T208 353-354 DT denotes a
T209 369-376 NN denotes disease
T210 355-360 JJ denotes human
T211 361-368 JJ denotes genetic
T212 377-387 VBN denotes associated
T213 388-392 IN denotes with
T214 393-400 NNS denotes defects
T215 401-403 IN denotes in
T216 404-408 JJ denotes such
T217 409-417 NN denotes proteins
T218 417-418 . denotes .
T219 418-675 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 419-421 TO denotes To
T221 429-439 VB denotes understand
T222 422-428 RBR denotes better
T223 594-605 VBD denotes inactivated
T224 440-443 DT denotes the
T225 444-448 NN denotes role
T227 452-456 NN denotes ATRX
T228 457-459 IN denotes in
T229 460-471 NN denotes development
T230 472-475 CC denotes and
T231 476-479 DT denotes the
T232 491-504 NNS denotes abnormalities
T233 480-490 VBN denotes associated
T234 505-507 IN denotes in
T235 508-511 DT denotes the
T236 567-575 NN denotes syndrome
T237 512-515 NN denotes ATR
T238 516-517 NN denotes X
T239 515-516 HYPH denotes -
T240 518-519 -LRB- denotes (
T241 519-524 NN denotes alpha
T242 525-536 NN denotes thalassemia
T243 537-543 JJ denotes mental
T244 544-555 NN denotes retardation
T245 555-557 , denotes ,
T246 557-558 NN denotes X
T247 559-565 VBN denotes linked
T248 558-559 HYPH denotes -
T249 565-566 -RRB- denotes )
T250 575-577 , denotes ,
T251 577-579 PRP denotes we
T252 580-593 RB denotes conditionally
T253 606-609 DT denotes the
T254 610-617 NN denotes homolog
T255 618-620 IN denotes in
T256 621-625 NNS denotes mice
T257 625-627 , denotes ,
T258 627-631 NN denotes Atrx
T259 631-633 , denotes ,
T260 633-635 IN denotes at
T261 636-639 DT denotes the
T262 654-659 NN denotes stage
T263 640-641 CD denotes 8
T264 646-648 CD denotes 16
T265 641-642 HYPH denotes -
T266 643-645 IN denotes to
T267 649-653 NN denotes cell
T268 648-649 HYPH denotes -
T269 660-662 IN denotes of
T270 663-674 NN denotes development
T271 674-675 . denotes .
T272 675-977 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 676-679 DT denotes The
T274 680-687 NN denotes protein
T275 712-721 VBN denotes expressed
T276 687-689 , denotes ,
T277 689-693 NN denotes Atrx
T278 693-695 , denotes ,
T279 695-698 VBD denotes was
T280 699-711 RB denotes ubiquitously
T281 721-723 , denotes ,
T282 723-726 CC denotes and
T283 727-731 JJ denotes male
T284 732-739 NNS denotes embryos
T285 754-763 VBN denotes implanted
T286 740-744 JJ denotes null
T287 745-748 IN denotes for
T288 749-753 NN denotes Atrx
T289 764-767 CC denotes and
T290 768-779 VBN denotes gastrulated
T291 780-788 RB denotes normally
T292 789-792 CC denotes but
T293 793-796 VBD denotes did
T294 801-808 VB denotes survive
T295 797-800 RB denotes not
T296 809-815 IN denotes beyond
T297 816-819 CD denotes 9.5
T298 820-824 NNS denotes days
T299 825-835 RB denotes postcoitus
T300 836-839 IN denotes due
T301 840-842 IN denotes to
T302 843-844 DT denotes a
T303 845-851 NN denotes defect
T304 852-854 IN denotes in
T305 855-864 NN denotes formation
T306 865-867 IN denotes of
T307 868-871 DT denotes the
T308 887-898 NN denotes trophoblast
T309 872-886 JJ denotes extraembryonic
T310 898-900 , denotes ,
T311 900-903 CD denotes one
T312 904-906 IN denotes of
T313 907-910 DT denotes the
T314 943-951 NNS denotes lineages
T315 911-916 JJ denotes first
T316 917-927 RB denotes terminally
T317 928-942 VBN denotes differentiated
T318 952-954 IN denotes in
T319 955-958 DT denotes the
T320 970-976 NN denotes embryo
T321 959-969 VBG denotes developing
T322 976-977 . denotes .
T323 977-1136 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 978-985 NN denotes Carrier
T325 993-997 NNS denotes mice
T326 986-992 JJ denotes female
T327 1044-1052 VBN denotes affected
T328 998-1002 WDT denotes that
T329 1003-1010 VBP denotes inherit
T330 1011-1012 DT denotes a
T331 1027-1033 NN denotes allele
T332 1013-1021 JJ denotes maternal
T333 1022-1026 JJ denotes null
T334 1034-1040 MD denotes should
T335 1041-1043 VB denotes be
T336 1052-1054 , denotes ,
T337 1054-1059 IN denotes since
T338 1086-1088 VBZ denotes is
T339 1060-1063 DT denotes the
T340 1075-1085 NN denotes chromosome
T341 1064-1072 JJ denotes paternal
T342 1073-1074 NN denotes X
T343 1089-1097 RB denotes normally
T344 1098-1109 JJ denotes inactivated
T345 1110-1112 IN denotes in
T346 1113-1127 JJ denotes extraembryonic
T347 1128-1135 NNS denotes tissues
T348 1135-1136 . denotes .
T349 1136-1297 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 1137-1149 RB denotes Surprisingly
T351 1181-1192 VBD denotes established
T352 1149-1151 , denotes ,
T353 1151-1158 RB denotes however
T354 1158-1160 , denotes ,
T355 1160-1164 DT denotes some
T356 1173-1180 NNS denotes females
T357 1165-1172 NN denotes carrier
T358 1193-1194 DT denotes a
T359 1202-1210 NN denotes placenta
T360 1195-1201 JJ denotes normal
T361 1211-1214 CC denotes and
T362 1215-1223 VBD denotes appeared
T363 1224-1226 TO denotes to
T364 1227-1233 VB denotes escape
T365 1234-1237 DT denotes the
T366 1244-1251 NN denotes pattern
T367 1238-1243 JJ denotes usual
T368 1252-1254 IN denotes of
T369 1255-1264 VBN denotes imprinted
T370 1267-1279 NN denotes inactivation
T371 1265-1266 NN denotes X
T372 1266-1267 HYPH denotes -
T373 1280-1282 IN denotes in
T374 1283-1288 DT denotes these
T375 1289-1296 NNS denotes tissues
T376 1296-1297 . denotes .
T377 1297-1506 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 1298-1306 RB denotes Together
T379 1322-1333 VBP denotes demonstrate
T380 1307-1312 DT denotes these
T381 1313-1321 NNS denotes findings
T382 1334-1336 DT denotes an
T383 1373-1377 NN denotes role
T384 1337-1347 JJ denotes unexpected
T385 1347-1349 , denotes ,
T386 1349-1357 JJ denotes specific
T387 1357-1359 , denotes ,
T388 1359-1362 CC denotes and
T389 1363-1372 JJ denotes essential
T390 1378-1381 IN denotes for
T391 1382-1386 NN denotes Atrx
T392 1387-1389 IN denotes in
T393 1390-1393 DT denotes the
T394 1394-1405 NN denotes development
T395 1406-1408 IN denotes of
T396 1409-1412 DT denotes the
T397 1420-1431 NN denotes trophoblast
T398 1413-1419 JJ denotes murine
T399 1432-1435 CC denotes and
T400 1436-1443 VBP denotes present
T401 1444-1446 DT denotes an
T402 1447-1454 NN denotes example
T403 1455-1457 IN denotes of
T404 1458-1464 NN denotes escape
T405 1465-1469 IN denotes from
T406 1470-1479 VBN denotes imprinted
T407 1482-1492 NN denotes chromosome
T408 1480-1481 NN denotes X
T409 1493-1505 NN denotes inactivation
T410 1505-1506 . denotes .
T160 49-52 DT denotes the
R7 T161 T158 conj Pattern,Development
R8 T162 T161 prep of,Pattern
R9 T163 T164 compound X,Inactivation
R10 T164 T162 pobj Inactivation,of
R12 T166 T153 prep in,Affects
R13 T167 T168 amod Extraembryonic,Tissues
R14 T168 T166 pobj Tissues,in
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
R242 T160 T161 det the,Pattern
R1 T152 T153 nsubj Loss,Affects
R2 T155 T152 prep of,Loss
R3 T156 T155 pobj Atrx,of
R4 T157 T158 compound Trophoblast,Development
R5 T158 T153 dobj Development,Affects
R6 T159 T158 cc and,Development
R11 T165 T164 punct -,Inactivation
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
T92 8-12 PR_EXT:000004503 denotes Atrx
T93 21-32 UBERON:0000088 denotes Trophoblast
T94 64-65 GO:0000805 denotes X
T95 64-78 GO:0009048 denotes X-Inactivation
T96 82-104 UBERON:0005292 denotes Extraembryonic Tissues
T97 155-159 PR_EXT:000004503 denotes ATRX
T98 166-167 GO:0000805 denotes X
T99 168-175 SO_EXT:sequence_coding_function denotes encoded
T100 190-194 PR_EXT:P22082 denotes SNF2
T101 205-211 GO_EXT:0016887 denotes ATPase
T102 212-220 GO_EXT:0004386 denotes helicase
T103 221-229 CHEBI_PR_EXT:protein denotes proteins
T104 241-249 GO:0065007 denotes regulate
T105 250-254 SO_EXT:0000704 denotes gene
T106 250-265 GO:0010467 denotes gene expression
T107 279-288 GO:0000785 denotes chromatin
T108 305-314 SO_EXT:sequence_alteration_entity_or_process denotes Mutations
T109 318-322 PR_EXT:000004503 denotes ATRX
T110 355-360 NCBITaxon:9606 denotes human
T111 361-368 SO_EXT:0000704 denotes genetic
T112 409-417 CHEBI_PR_EXT:protein denotes proteins
T113 452-456 PR_EXT:000004503 denotes ATRX
T114 516-517 GO:0000805 denotes X
T115 557-558 GO:0000805 denotes X
T116 610-617 SO_EXT:0000853 denotes homolog
T117 621-625 NCBITaxon:10088 denotes mice
T118 627-631 PR_EXT:000004503 denotes Atrx
T119 649-653 CL_GO_EXT:cell denotes cell
T120 680-687 CHEBI_PR_EXT:protein denotes protein
T121 689-693 PR_EXT:000004503 denotes Atrx
T122 712-721 GO:0010467 denotes expressed
T123 727-731 PATO_UBERON_EXT:male_or_bearer_of_maleness denotes male
T124 732-739 UBERON:0000922 denotes embryos
T125 740-744 SO_EXT:sequence_nullness denotes null
T126 749-753 PR_EXT:000004503 denotes Atrx
T127 754-763 GO:0007566 denotes implanted
T128 768-779 GO:0007369 denotes gastrulated
T129 829-835 GO:0007620 denotes coitus
T130 877-886 UBERON:0000922 denotes embryonic
T131 887-898 UBERON:0000088 denotes trophoblast
T132 928-942 GO_PATO_RO_EXT:developmental_differentiation_process_or_quality denotes differentiated
T133 970-976 UBERON:0000922 denotes embryo
T134 986-992 PATO_UBERON_EXT:female_or_bearer_of_femaleness denotes female
T135 993-997 NCBITaxon:10088 denotes mice
T136 1022-1026 SO_EXT:sequence_nullness denotes null
T137 1027-1033 SO_EXT:0001023 denotes allele
T138 1073-1085 GO:0000805 denotes X chromosome
T139 1075-1085 GO_SO_EXT:chromosome denotes chromosome
T140 1113-1135 UBERON:0005292 denotes extraembryonic tissues
T141 1173-1180 PATO_UBERON_EXT:female_or_bearer_of_femaleness denotes females
T142 1202-1210 UBERON:0001987 denotes placenta
T143 1255-1279 GO:0060819 denotes imprinted X-inactivation
T144 1265-1266 GO:0000805 denotes X
T145 1289-1296 UBERON:0000479 denotes tissues
T146 1382-1386 PR_EXT:000004503 denotes Atrx
T147 1413-1419 NCBITaxon:39107 denotes murine
T148 1420-1431 UBERON:0000088 denotes trophoblast
T149 1470-1505 GO:0060819 denotes imprinted X chromosome inactivation
T150 1480-1492 GO:0000805 denotes X chromosome
T151 1482-1492 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
T48 8-12 PR:000004503 denotes Atrx
T49 21-32 UBERON:0000088 denotes Trophoblast
T50 64-65 GO:0000805 denotes X
T51 64-78 GO:0009048 denotes X-Inactivation
T52 82-104 UBERON:0005292 denotes Extraembryonic Tissues
T53 155-159 PR:000004503 denotes ATRX
T54 166-167 GO:0000805 denotes X
T55 190-194 PR:P22082 denotes SNF2
T56 241-249 GO:0065007 denotes regulate
T57 250-254 SO:0000704 denotes gene
T58 250-265 GO:0010467 denotes gene expression
T59 279-288 GO:0000785 denotes chromatin
T60 318-322 PR:000004503 denotes ATRX
T61 355-360 NCBITaxon:9606 denotes human
T62 361-368 SO:0000704 denotes genetic
T63 452-456 PR:000004503 denotes ATRX
T64 516-517 GO:0000805 denotes X
T65 557-558 GO:0000805 denotes X
T66 610-617 SO:0000853 denotes homolog
T67 621-625 NCBITaxon:10088 denotes mice
T68 627-631 PR:000004503 denotes Atrx
T69 689-693 PR:000004503 denotes Atrx
T70 712-721 GO:0010467 denotes expressed
T71 732-739 UBERON:0000922 denotes embryos
T72 749-753 PR:000004503 denotes Atrx
T73 754-763 GO:0007566 denotes implanted
T74 768-779 GO:0007369 denotes gastrulated
T75 829-835 GO:0007620 denotes coitus
T76 877-886 UBERON:0000922 denotes embryonic
T77 887-898 UBERON:0000088 denotes trophoblast
T78 970-976 UBERON:0000922 denotes embryo
T79 993-997 NCBITaxon:10088 denotes mice
T80 1027-1033 SO:0001023 denotes allele
T81 1073-1085 GO:0000805 denotes X chromosome
T82 1113-1135 UBERON:0005292 denotes extraembryonic tissues
T83 1202-1210 UBERON:0001987 denotes placenta
T84 1255-1279 GO:0060819 denotes imprinted X-inactivation
T85 1265-1266 GO:0000805 denotes X
T86 1289-1296 UBERON:0000479 denotes tissues
T87 1382-1386 PR:000004503 denotes Atrx
T88 1413-1419 NCBITaxon:39107 denotes murine
T89 1420-1431 UBERON:0000088 denotes trophoblast
T90 1470-1505 GO:0060819 denotes imprinted X chromosome inactivation
T91 1480-1492 GO:0000805 denotes X chromosome