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PMC:1208879 / 0-350 JSONTXT 4 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue
T175 0-1 DT denotes A
T177 0-117 sentence denotes A screen for proteins that interact with PAX6: C-terminal mutations disrupt interaction with HOMER3, DNCL1 and TRIM11
T176 2-8 NN denotes screen
T179 9-12 IN denotes for
T180 13-21 NN denotes proteins
T181 22-26 WDT denotes that
T182 27-35 VBP denotes interact
T183 36-40 IN denotes with
T184 41-45 NN denotes PAX6
T185 45-47 : denotes :
T186 47-48 NN denotes C
T188 48-49 HYPH denotes -
T187 49-57 JJ denotes terminal
T189 58-67 NNS denotes mutations
T178 68-75 VBP denotes disrupt
T190 76-87 NN denotes interaction
T191 88-92 IN denotes with
T192 93-99 NN denotes HOMER3
T193 99-101 , denotes ,
T194 101-106 NN denotes DNCL1
T195 107-110 CC denotes and
T196 111-117 NN denotes TRIM11
T197 117-118 sentence denotes
T198 128-138 sentence denotes Background
T199 128-138 NN denotes Background
T200 138-242 sentence denotes The PAX6 protein is a transcriptional regulator with a key role in ocular and neurological development.
T201 139-142 DT denotes The
T203 143-147 NN denotes PAX6
T202 148-155 NN denotes protein
T204 156-158 VBZ denotes is
T205 159-160 DT denotes a
T207 161-176 JJ denotes transcriptional
T206 177-186 NN denotes regulator
T208 187-191 IN denotes with
T209 192-193 DT denotes a
T211 194-197 JJ denotes key
T210 198-202 NN denotes role
T212 203-205 IN denotes in
T213 206-212 JJ denotes ocular
T215 213-216 CC denotes and
T216 217-229 JJ denotes neurological
T214 230-241 NN denotes development
T217 241-242 . denotes .
T219 243-254 NNS denotes Individuals
T221 255-259 IN denotes with
T222 260-272 JJ denotes heterozygous
T224 273-277 NN denotes loss
T225 277-278 HYPH denotes -
T226 278-280 IN denotes of
T227 280-281 HYPH denotes -
T228 281-289 NN denotes function
T223 290-299 NNS denotes mutations
T229 300-302 IN denotes in
T230 303-306 DT denotes the
T232 307-311 NN denotes PAX6
T231 312-316 NN denotes gene
T220 317-321 VBP denotes have
T233 322-335 NNS denotes malformations
T234 336-338 IN denotes of
T235 339-342 DT denotes the
T236 343-346 NN denotes eye
T237 347-350 CC denotes and
R10 T186 T187 npadvmod C,terminal
R11 T187 T189 amod terminal,mutations
R12 T188 T187 punct -,terminal
R13 T189 T178 nsubj mutations,disrupt
R14 T190 T178 dobj interaction,disrupt
R15 T191 T190 prep with,interaction
R16 T192 T191 pobj HOMER3,with
R17 T193 T192 punct ", ",HOMER3
R18 T194 T192 conj DNCL1,HOMER3
R19 T195 T194 cc and,DNCL1
R2 T176 T178 dep screen,disrupt
R20 T196 T194 conj TRIM11,DNCL1
R21 T201 T202 det The,protein
R22 T202 T204 nsubj protein,is
R23 T203 T202 compound PAX6,protein
R24 T205 T206 det a,regulator
R25 T206 T204 attr regulator,is
R250 T175 T176 det A,screen
R26 T207 T206 amod transcriptional,regulator
R27 T208 T206 prep with,regulator
R28 T209 T210 det a,role
R29 T210 T208 pobj role,with
R3 T179 T176 prep for,screen
R30 T211 T210 amod key,role
R31 T212 T210 prep in,role
R32 T213 T214 amod ocular,development
R33 T214 T212 pobj development,in
R34 T215 T213 cc and,ocular
R35 T216 T213 conj neurological,ocular
R36 T217 T204 punct .,is
R37 T219 T220 nsubj Individuals,have
R38 T221 T219 prep with,Individuals
R39 T222 T223 amod heterozygous,mutations
R4 T180 T179 pobj proteins,for
R40 T223 T221 pobj mutations,with
R41 T224 T223 nmod loss,mutations
R42 T225 T224 punct -,loss
R43 T226 T224 prep of,loss
R44 T227 T226 punct -,of
R45 T228 T226 pobj function,of
R46 T229 T219 prep in,Individuals
R47 T230 T231 det the,gene
R48 T231 T229 pobj gene,in
R49 T232 T231 compound PAX6,gene
R5 T181 T182 dep that,interact
R50 T233 T220 dobj malformations,have
R51 T234 T233 prep of,malformations
R52 T235 T236 det the,eye
R53 T236 T234 pobj eye,of
R54 T237 T236 cc and,eye
R6 T182 T180 relcl interact,proteins
R7 T183 T182 prep with,interact
R8 T184 T183 pobj PAX6,with
R9 T185 T178 punct : ,disrupt