> top > docs > PMC:516044 > spans > 129-446 > annotations

PMC:516044 / 129-446 JSONTXT

Annnotations TAB JSON ListView MergeView

craft-sa-dev

Id Subject Object Predicate Lexical cue
T253 0-10 NN denotes Background
T254 10-175 sentence denotes Pendred syndrome, a common autosomal-recessive disorder characterized by congenital deafness and goiter, is caused by mutations of SLC26A4, which codes for pendrin.
T255 11-18 NNP denotes Pendred
T256 19-27 NN denotes syndrome
T257 119-125 VBN denotes caused
T258 27-29 , denotes ,
T259 29-30 DT denotes a
T260 58-66 NN denotes disorder
T261 31-37 JJ denotes common
T262 38-47 JJ denotes autosomal
T263 48-57 JJ denotes recessive
T264 47-48 HYPH denotes -
T265 67-80 VBN denotes characterized
T266 81-83 IN denotes by
T267 84-94 JJ denotes congenital
T268 95-103 NN denotes deafness
T269 104-107 CC denotes and
T270 108-114 NN denotes goiter
T271 114-116 , denotes ,
T272 116-118 VBZ denotes is
T273 126-128 IN denotes by
T274 129-138 NNS denotes mutations
T275 139-141 IN denotes of
T276 142-149 NN denotes SLC26A4
T277 149-151 , denotes ,
T278 151-156 WDT denotes which
T279 157-162 VBZ denotes codes
T280 163-166 IN denotes for
T281 167-174 NN denotes pendrin
T282 174-175 . denotes .
T283 175-317 sentence denotes We investigated the relationship between pendrin and deafness using mice that have (Slc26a4+/+) or lack a complete Slc26a4 gene (Slc26a4-/-).
T284 176-178 PRP denotes We
T285 179-191 VBD denotes investigated
T286 192-195 DT denotes the
T287 196-208 NN denotes relationship
T288 209-216 IN denotes between
T289 217-224 NN denotes pendrin
T290 225-228 CC denotes and
T291 229-237 NN denotes deafness
T292 238-243 VBG denotes using
T293 244-248 NNS denotes mice
T294 249-253 WDT denotes that
T295 254-258 VBP denotes have
T296 259-260 -LRB- denotes (
T297 260-267 NN denotes Slc26a4
T298 267-268 SYM denotes +
T299 268-269 HYPH denotes /
T300 269-270 SYM denotes +
T301 270-271 -RRB- denotes )
T302 272-274 CC denotes or
T303 275-279 VBP denotes lack
T304 280-281 DT denotes a
T305 299-303 NN denotes gene
T306 282-290 JJ denotes complete
T307 291-298 NN denotes Slc26a4
T308 304-305 -LRB- denotes (
T309 314-315 SYM denotes -
T310 305-312 NN denotes Slc26a4
T311 312-313 SYM denotes -
T312 313-314 HYPH denotes /
T313 315-316 -RRB- denotes )
T314 316-317 . denotes .
T252 0-10 sentence denotes Background
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 38-47 GO:0030849 denotes autosomal
T145 129-138 SO_EXT:sequence_alteration_entity_or_process denotes mutations
T146 142-149 PR_EXT:000015039 denotes SLC26A4
T147 157-162 SO_EXT:sequence_coding_function denotes codes
T148 167-174 PR_EXT:000015039 denotes pendrin
T149 217-224 PR_EXT:000015039 denotes pendrin
T150 244-248 NCBITaxon:10088 denotes mice
T151 260-267 PR_EXT:000015039 denotes Slc26a4
T152 267-268 SO_EXT:normal_or_wild_type_or_present denotes +
T153 269-270 SO_EXT:normal_or_wild_type_or_present denotes +
T154 291-298 PR_EXT:000015039 denotes Slc26a4
T155 299-303 SO_EXT:0000704 denotes gene
T156 305-312 PR_EXT:000015039 denotes Slc26a4
T157 312-313 SO_EXT:sequence_nullness_or_absence denotes -
T158 314-315 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 38-47 GO:0030849 denotes autosomal
T82 142-149 PR:000015039 denotes SLC26A4
T83 167-174 PR:000015039 denotes pendrin
T84 217-224 PR:000015039 denotes pendrin
T85 244-248 NCBITaxon:10088 denotes mice
T86 260-267 PR:000015039 denotes Slc26a4
T87 291-298 PR:000015039 denotes Slc26a4
T88 299-303 SO:0000704 denotes gene
T89 305-312 PR:000015039 denotes Slc26a4