PMC:516044 / 129-446 4 Projects
Annnotations
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T253 | 0-10 | NN | denotes | Background |
| T252 | 0-10 | sentence | 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 |
| T258 | 27-29 | , | denotes | , |
| T259 | 29-30 | DT | denotes | a |
| T261 | 31-37 | JJ | denotes | common |
| T262 | 38-47 | JJ | denotes | autosomal |
| T264 | 47-48 | HYPH | denotes | - |
| T263 | 48-57 | JJ | denotes | recessive |
| T260 | 58-66 | NN | denotes | disorder |
| 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 |
| T257 | 119-125 | VBN | denotes | caused |
| 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 |
| T306 | 282-290 | JJ | denotes | complete |
| T307 | 291-298 | NN | denotes | Slc26a4 |
| T305 | 299-303 | NN | denotes | gene |
| T308 | 304-305 | -LRB- | denotes | ( |
| T310 | 305-312 | NN | denotes | Slc26a4 |
| T311 | 312-313 | SYM | denotes | - |
| T312 | 313-314 | HYPH | denotes | / |
| T309 | 314-315 | SYM | denotes | - |
| T313 | 315-316 | -RRB- | denotes | ) |
| T314 | 316-317 | . | denotes | . |
| 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 |
| 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 |