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PMC:1626108 / 1232-1516 JSONTXT 4 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue
T439 1-9 NN denotes activity
T441 10-12 IN denotes of
T442 13-18 NN denotes Cox11
T443 19-23 IN denotes over
T444 24-27 NN denotes HKI
T445 27-28 . denotes .
T446 28-176 sentence denotes To probe the physiological role of RanBP2 and its role in HKI function, a mouse model harboring a genetically disrupted RanBP2 locus was generated.
T447 29-31 TO denotes To
T448 32-37 VB denotes probe
T450 38-41 DT denotes the
T452 42-55 JJ denotes physiological
T451 56-60 NN denotes role
T453 61-63 IN denotes of
T454 64-70 NN denotes RanBP2
T455 71-74 CC denotes and
T456 75-78 PRP$ denotes its
T457 79-83 NN denotes role
T458 84-86 IN denotes in
T459 87-90 NN denotes HKI
T460 91-99 NN denotes function
T461 99-101 , denotes ,
T462 101-102 DT denotes a
T464 103-108 NN denotes mouse
T463 109-114 NN denotes model
T465 115-124 VBG denotes harboring
T466 125-126 DT denotes a
T468 127-138 RB denotes genetically
T469 139-148 VBN denotes disrupted
T470 149-155 NN denotes RanBP2
T467 156-161 NN denotes locus
T471 162-165 VBD denotes was
T449 166-175 VBN denotes generated
T472 175-176 . denotes .
T474 177-183 NN denotes RanBP2
T476 183-184 SYM denotes −
T477 184-185 HYPH denotes /
T478 185-186 SYM denotes −
T475 187-190 VBP denotes are
T479 191-204 RB denotes embryonically
T480 205-211 JJ denotes lethal
T481 211-213 , denotes ,
T482 213-216 CC denotes and
T483 217-235 NN denotes haploinsufficiency
T485 236-238 IN denotes of
T486 239-245 NN denotes RanBP2
T487 246-248 IN denotes in
T488 249-251 DT denotes an
T490 252-258 JJ denotes inbred
T489 259-265 NN denotes strain
T484 266-272 VBZ denotes causes
T491 273-274 DT denotes a
R194 T441 T439 prep of,activity
R195 T442 T441 pobj Cox11,of
R196 T443 T439 prep over,activity
R197 T444 T443 pobj HKI,over
R199 T447 T448 aux To,probe
R200 T448 T449 advcl probe,generated
R201 T450 T451 det the,role
R202 T451 T448 dobj role,probe
R203 T452 T451 amod physiological,role
R204 T453 T451 prep of,role
R205 T454 T453 pobj RanBP2,of
R206 T455 T451 cc and,role
R207 T456 T457 poss its,role
R208 T457 T451 conj role,role
R209 T458 T457 prep in,role
R210 T459 T460 compound HKI,function
R211 T460 T458 pobj function,in
R212 T461 T449 punct ", ",generated
R213 T462 T463 det a,model
R214 T463 T449 nsubjpass model,generated
R215 T464 T463 compound mouse,model
R216 T465 T463 acl harboring,model
R217 T466 T467 det a,locus
R218 T467 T465 dobj locus,harboring
R219 T468 T469 advmod genetically,disrupted
R220 T469 T467 amod disrupted,locus
R221 T470 T467 compound RanBP2,locus
R222 T471 T449 auxpass was,generated
R223 T472 T449 punct .,generated
R224 T474 T475 nsubj RanBP2,are
R225 T476 T474 punct −,RanBP2
R226 T477 T474 punct /,RanBP2
R227 T478 T474 punct −,RanBP2
R228 T479 T480 advmod embryonically,lethal
R229 T480 T475 acomp lethal,are
R230 T481 T475 punct ", ",are
R231 T482 T475 cc and,are
R232 T483 T484 nsubj haploinsufficiency,causes
R233 T484 T475 conj causes,are
R234 T485 T483 prep of,haploinsufficiency
R235 T486 T485 pobj RanBP2,of
R236 T487 T483 prep in,haploinsufficiency
R237 T488 T489 det an,strain
R238 T489 T487 pobj strain,in
R239 T490 T489 amod inbred,strain