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PMC:516044 / 140-446 JSONTXT

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craft-sa-dev

Id Subject Object Predicate Lexical cue
T255 0-7 NNP denotes Pendred
T256 8-16 NN denotes syndrome
T257 108-114 VBN denotes caused
T258 16-18 , denotes ,
T259 18-19 DT denotes a
T260 47-55 NN denotes disorder
T261 20-26 JJ denotes common
T262 27-36 JJ denotes autosomal
T263 37-46 JJ denotes recessive
T264 36-37 HYPH denotes -
T265 56-69 VBN denotes characterized
T266 70-72 IN denotes by
T267 73-83 JJ denotes congenital
T268 84-92 NN denotes deafness
T269 93-96 CC denotes and
T270 97-103 NN denotes goiter
T271 103-105 , denotes ,
T272 105-107 VBZ denotes is
T273 115-117 IN denotes by
T274 118-127 NNS denotes mutations
T275 128-130 IN denotes of
T276 131-138 NN denotes SLC26A4
T277 138-140 , denotes ,
T278 140-145 WDT denotes which
T279 146-151 VBZ denotes codes
T280 152-155 IN denotes for
T281 156-163 NN denotes pendrin
T282 163-164 . denotes .
T283 164-306 sentence denotes We investigated the relationship between pendrin and deafness using mice that have (Slc26a4+/+) or lack a complete Slc26a4 gene (Slc26a4-/-).
T284 165-167 PRP denotes We
T285 168-180 VBD denotes investigated
T286 181-184 DT denotes the
T287 185-197 NN denotes relationship
T288 198-205 IN denotes between
T289 206-213 NN denotes pendrin
T290 214-217 CC denotes and
T291 218-226 NN denotes deafness
T292 227-232 VBG denotes using
T293 233-237 NNS denotes mice
T294 238-242 WDT denotes that
T295 243-247 VBP denotes have
T296 248-249 -LRB- denotes (
T297 249-256 NN denotes Slc26a4
T298 256-257 SYM denotes +
T299 257-258 HYPH denotes /
T300 258-259 SYM denotes +
T301 259-260 -RRB- denotes )
T302 261-263 CC denotes or
T303 264-268 VBP denotes lack
T304 269-270 DT denotes a
T305 288-292 NN denotes gene
T306 271-279 JJ denotes complete
T307 280-287 NN denotes Slc26a4
T308 293-294 -LRB- denotes (
T309 303-304 SYM denotes -
T310 294-301 NN denotes Slc26a4
T311 301-302 SYM denotes -
T312 302-303 HYPH denotes /
T313 304-305 -RRB- denotes )
T314 305-306 . denotes .
R36 T270 T268 conj goiter,deafness
R35 T269 T268 cc and,deafness
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
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
R44 T278 T279 dep which,codes
R45 T279 T276 relcl codes,SLC26A4
R46 T280 T279 prep for,codes
R47 T281 T280 pobj pendrin,for
R48 T282 T257 punct .,caused
R49 T284 T285 nsubj We,investigated
R50 T286 T287 det the,relationship
R51 T287 T285 dobj relationship,investigated
R52 T288 T287 prep between,relationship
R53 T289 T288 pobj pendrin,between
R54 T290 T289 cc and,pendrin
R55 T291 T289 conj deafness,pendrin
R56 T292 T285 advcl using,investigated
R57 T293 T292 dobj mice,using
R58 T294 T295 dep that,have
R59 T295 T293 relcl have,mice
R60 T296 T297 punct (,Slc26a4
R61 T297 T295 parataxis Slc26a4,have
R62 T298 T297 punct +,Slc26a4
R63 T299 T297 punct /,Slc26a4
R64 T300 T297 punct +,Slc26a4
R65 T301 T297 punct ),Slc26a4
R66 T302 T295 cc or,have
R67 T303 T295 conj lack,have
R68 T304 T305 det a,gene
R69 T305 T303 dobj gene,lack
R70 T306 T305 amod complete,gene
R71 T307 T305 compound Slc26a4,gene
R72 T308 T309 punct (,-
R73 T309 T303 punct -,lack
R74 T310 T309 nmod Slc26a4,-
R75 T311 T309 punct -,-
R76 T312 T309 punct /,-
R77 T313 T309 punct ),-
R78 T314 T285 punct .,investigated

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
T144 27-36 GO:0030849 denotes autosomal
T145 118-127 SO_EXT:sequence_alteration_entity_or_process denotes mutations
T146 131-138 PR_EXT:000015039 denotes SLC26A4
T147 146-151 SO_EXT:sequence_coding_function denotes codes
T148 156-163 PR_EXT:000015039 denotes pendrin
T149 206-213 PR_EXT:000015039 denotes pendrin
T150 233-237 NCBITaxon:10088 denotes mice
T151 249-256 PR_EXT:000015039 denotes Slc26a4
T152 256-257 SO_EXT:normal_or_wild_type_or_present denotes +
T153 258-259 SO_EXT:normal_or_wild_type_or_present denotes +
T154 280-287 PR_EXT:000015039 denotes Slc26a4
T155 288-292 SO_EXT:0000704 denotes gene
T156 294-301 PR_EXT:000015039 denotes Slc26a4
T157 301-302 SO_EXT:sequence_nullness_or_absence denotes -
T158 303-304 SO_EXT:sequence_nullness_or_absence denotes -

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
T81 27-36 GO:0030849 denotes autosomal
T82 131-138 PR:000015039 denotes SLC26A4
T83 156-163 PR:000015039 denotes pendrin
T84 206-213 PR:000015039 denotes pendrin
T85 233-237 NCBITaxon:10088 denotes mice
T86 249-256 PR:000015039 denotes Slc26a4
T87 280-287 PR:000015039 denotes Slc26a4
T88 288-292 SO:0000704 denotes gene
T89 294-301 PR:000015039 denotes Slc26a4