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PMC:516044 / 164-306 JSONTXT

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craft-sa-dev

Id Subject Object Predicate Lexical cue
T257 84-90 VBN denotes caused
T260 23-31 NN denotes disorder
T262 3-12 JJ denotes autosomal
T263 13-22 JJ denotes recessive
T264 12-13 HYPH denotes -
T265 32-45 VBN denotes characterized
T266 46-48 IN denotes by
T267 49-59 JJ denotes congenital
T268 60-68 NN denotes deafness
T269 69-72 CC denotes and
T270 73-79 NN denotes goiter
T271 79-81 , denotes ,
T272 81-83 VBZ denotes is
T273 91-93 IN denotes by
T274 94-103 NNS denotes mutations
T275 104-106 IN denotes of
T276 107-114 NN denotes SLC26A4
T277 114-116 , denotes ,
T278 116-121 WDT denotes which
T279 122-127 VBZ denotes codes
T280 128-131 IN denotes for
T281 132-139 NN denotes pendrin
T282 139-140 . denotes .
R36 T270 T268 conj goiter,deafness
R35 T269 T268 cc and,deafness
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

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 3-12 GO:0030849 denotes autosomal
T145 94-103 SO_EXT:sequence_alteration_entity_or_process denotes mutations
T146 107-114 PR_EXT:000015039 denotes SLC26A4
T147 122-127 SO_EXT:sequence_coding_function denotes codes
T148 132-139 PR_EXT:000015039 denotes pendrin

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 3-12 GO:0030849 denotes autosomal
T82 107-114 PR:000015039 denotes SLC26A4
T83 132-139 PR:000015039 denotes pendrin