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PMC:516044 / 0-286 JSONTXT 4 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue
T234 0-4 NN denotes Loss
T236 0-118 sentence denotes Loss of KCNJ10 protein expression abolishes endocochlear potential and causes deafness in Pendred syndrome mouse model
T237 5-7 IN denotes of
T238 8-14 NN denotes KCNJ10
T240 15-22 NN denotes protein
T239 23-33 NN denotes expression
T235 34-43 VBZ denotes abolishes
T241 44-56 JJ denotes endocochlear
T242 57-66 NN denotes potential
T243 67-70 CC denotes and
T244 71-77 VBZ denotes causes
T245 78-86 NN denotes deafness
T246 87-89 IN denotes in
T247 90-97 NNP denotes Pendred
T248 98-106 NN denotes syndrome
T250 107-112 NN denotes mouse
T249 113-118 NN denotes model
T251 118-119 sentence denotes
T253 129-139 NN denotes Background
T252 129-139 sentence denotes Background
T255 140-147 NNP denotes Pendred
T256 148-156 NN denotes syndrome
T258 156-158 , denotes ,
T259 158-159 DT denotes a
T261 160-166 JJ denotes common
T262 167-176 JJ denotes autosomal
T264 176-177 HYPH denotes -
T263 177-186 JJ denotes recessive
T260 187-195 NN denotes disorder
T265 196-209 VBN denotes characterized
T266 210-212 IN denotes by
T267 213-223 JJ denotes congenital
T268 224-232 NN denotes deafness
T269 233-236 CC denotes and
T270 237-243 NN denotes goiter
T271 243-245 , denotes ,
T272 245-247 VBZ denotes is
T257 248-254 VBN denotes caused
T273 255-257 IN denotes by
T274 258-267 NNS denotes mutations
T275 268-270 IN denotes of
T276 271-278 NN denotes SLC26A4
T277 278-280 , denotes ,
T278 280-285 WDT denotes which
R10 T239 T237 pobj expression,of
R11 T240 T239 compound protein,expression
R12 T241 T242 amod endocochlear,potential
R13 T242 T235 dobj potential,abolishes
R14 T243 T235 cc and,abolishes
R15 T244 T235 conj causes,abolishes
R16 T245 T244 dobj deafness,causes
R17 T246 T244 prep in,causes
R18 T247 T248 compound Pendred,syndrome
R19 T248 T249 compound syndrome,model
R20 T249 T246 pobj model,in
R21 T250 T249 compound mouse,model
R22 T255 T256 compound Pendred,syndrome
R23 T256 T257 nsubjpass syndrome,caused
R24 T258 T256 punct ", ",syndrome
R25 T259 T260 det a,disorder
R26 T260 T256 appos disorder,syndrome
R27 T261 T260 amod common,disorder
R28 T262 T263 amod autosomal,recessive
R29 T263 T260 amod recessive,disorder
R30 T264 T263 punct -,recessive
R31 T265 T260 acl characterized,disorder
R32 T266 T265 agent by,characterized
R33 T267 T268 amod congenital,deafness
R34 T268 T266 pobj deafness,by
R35 T269 T268 cc and,deafness
R36 T270 T268 conj goiter,deafness
R37 T271 T257 punct ", ",caused
R38 T272 T257 auxpass is,caused
R39 T273 T257 agent by,caused
R40 T274 T273 pobj mutations,by
R41 T275 T274 prep of,mutations
R42 T276 T275 pobj SLC26A4,of
R43 T277 T276 punct ", ",SLC26A4
R7 T234 T235 nsubj Loss,abolishes
R8 T237 T234 prep of,Loss
R9 T238 T239 compound KCNJ10,expression