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PMC:314463 / 787-1105 JSONTXT 4 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue
T305 6-16 NN denotes expression
T308 17-19 IN denotes in
T309 20-30 VBG denotes developing
T310 31-41 NN denotes mesenchyme
T307 42-52 VBZ denotes correlates
T311 53-57 IN denotes with
T312 58-68 JJ denotes pigmentary
T314 69-72 CC denotes and
T315 73-81 JJ denotes skeletal
T313 82-95 NNS denotes malformations
T316 96-104 VBN denotes observed
T317 105-107 IN denotes in
T318 108-111 NN denotes deH
T320 111-112 HYPH denotes /
T319 112-115 NN denotes deH
T321 116-123 NNS denotes animals
T322 123-124 . denotes .
T323 124-238 sentence denotes Construction of a targeted allele of Tbx15 confirmed that the deH phenotype was caused by Tbx15 loss of function.
T324 125-137 NN denotes Construction
T326 138-140 IN denotes of
T327 141-142 DT denotes a
T329 143-151 VBN denotes targeted
T328 152-158 NN denotes allele
T330 159-161 IN denotes of
T331 162-167 NN denotes Tbx15
T325 168-177 VBD denotes confirmed
T332 178-182 IN denotes that
T334 183-186 DT denotes the
T336 187-190 NN denotes deH
T335 191-200 NN denotes phenotype
T337 201-204 VBD denotes was
T333 205-211 VBN denotes caused
T338 212-214 IN denotes by
T339 215-220 NN denotes Tbx15
T340 221-225 NN denotes loss
T341 226-228 IN denotes of
T342 229-237 NN denotes function
T343 237-238 . denotes .
T345 239-244 RB denotes Early
T346 245-254 JJ denotes embryonic
T347 255-265 NN denotes expression
T349 266-268 IN denotes of
T350 269-274 NN denotes Tbx15
T351 275-277 IN denotes in
T352 278-284 JJ denotes dorsal
T353 285-295 NN denotes mesenchyme
T348 296-298 VBZ denotes is
T355 299-312 JJ denotes complementary
T356 313-315 IN denotes to
R126 T305 T307 dep expression,correlates
R129 T308 T305 prep in,expression
R130 T309 T310 amod developing,mesenchyme
R131 T310 T308 pobj mesenchyme,in
R132 T311 T307 prep with,correlates
R133 T312 T313 amod pigmentary,malformations
R134 T313 T311 pobj malformations,with
R135 T314 T312 cc and,pigmentary
R136 T315 T312 conj skeletal,pigmentary
R137 T316 T313 acl observed,malformations
R138 T317 T316 prep in,observed
R139 T318 T319 compound deH,deH
R140 T319 T321 compound deH,animals
R141 T320 T319 punct /,deH
R142 T321 T317 pobj animals,in
R144 T324 T325 nsubj Construction,confirmed
R145 T326 T324 prep of,Construction
R146 T327 T328 det a,allele
R147 T328 T326 pobj allele,of
R148 T329 T328 amod targeted,allele
R149 T330 T328 prep of,allele
R150 T331 T330 pobj Tbx15,of
R151 T332 T333 mark that,caused
R152 T333 T325 ccomp caused,confirmed
R153 T334 T335 det the,phenotype
R154 T335 T333 nsubjpass phenotype,caused
R155 T336 T335 compound deH,phenotype
R156 T337 T333 auxpass was,caused
R157 T338 T333 agent by,caused
R158 T339 T340 compound Tbx15,loss
R159 T340 T338 pobj loss,by
R160 T341 T340 prep of,loss
R161 T342 T341 pobj function,of
R162 T343 T325 punct .,confirmed
R163 T345 T346 advmod Early,embryonic
R164 T346 T347 amod embryonic,expression
R165 T347 T348 nsubj expression,is
R167 T349 T347 prep of,expression
R168 T350 T349 pobj Tbx15,of
R169 T351 T347 prep in,expression
R170 T352 T353 amod dorsal,mesenchyme
R171 T353 T351 pobj mesenchyme,in
R172 T355 T348 acomp complementary,is
R173 T356 T355 prep to,complementary