PMC:516044 / 2102-2218 JSONTXT 4 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue
T781 7-9 IN denotes by
T782 10-18 NN denotes deafness
T783 19-22 CC denotes and
T784 23-29 NN denotes goiter
T785 30-31 -LRB- denotes [
T786 31-32 CD denotes 1
T787 32-33 -RRB- denotes ]
T788 33-34 . denotes .
T790 35-38 DT denotes The
T791 39-47 NN denotes syndrome
T793 48-50 VBZ denotes is
T792 51-57 VBN denotes caused
T794 58-60 IN denotes by
T795 61-70 NNS denotes mutations
T796 71-73 IN denotes of
T797 74-77 DT denotes the
T799 78-81 NN denotes PDS
T798 82-86 NN denotes gene
T800 87-94 NN denotes SLC26A4
T801 94-96 , denotes ,
T802 96-101 WDT denotes which
T803 102-107 VBZ denotes codes
T804 108-111 IN denotes for
T805 112-115 DT denotes the
R343 T782 T781 pobj deafness,by
R344 T783 T782 cc and,deafness
R345 T784 T782 conj goiter,deafness
R346 T785 T786 punct [,1
R348 T787 T786 punct ],1
R350 T790 T791 det The,syndrome
R351 T791 T792 nsubjpass syndrome,caused
R352 T793 T792 auxpass is,caused
R353 T794 T792 agent by,caused
R354 T795 T794 pobj mutations,by
R355 T796 T795 prep of,mutations
R356 T797 T798 det the,gene
R357 T798 T796 pobj gene,of
R358 T799 T798 compound PDS,gene
R359 T800 T798 appos SLC26A4,gene
R360 T801 T798 punct ", ",gene
R361 T802 T803 dep which,codes
R362 T803 T798 relcl codes,gene
R363 T804 T803 prep for,codes