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PMC:516044 / 1812-2102 JSONTXT 4 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue
T560 2-14 NNS denotes observations
T561 15-26 VBP denotes demonstrate
T562 27-31 IN denotes that
T564 32-39 NN denotes pendrin
T565 40-51 NN denotes dysfunction
T563 52-57 VBZ denotes leads
T566 58-60 IN denotes to
T567 61-62 DT denotes a
T568 63-67 NN denotes loss
T569 68-70 IN denotes of
T570 71-77 NN denotes KCNJ10
T572 78-85 NN denotes protein
T571 86-96 NN denotes expression
T573 97-100 CC denotes and
T574 101-102 DT denotes a
T575 103-107 NN denotes loss
T576 108-110 IN denotes of
T577 111-114 DT denotes the
T579 115-127 JJ denotes endocochlear
T578 128-137 NN denotes potential
T580 137-139 , denotes ,
T581 139-144 WDT denotes which
T583 145-148 MD denotes may
T582 149-151 VB denotes be
T584 152-155 DT denotes the
T586 156-162 JJ denotes direct
T585 163-168 NN denotes cause
T587 169-171 IN denotes of
T588 172-180 NN denotes deafness
T589 181-183 IN denotes in
T590 184-191 NNP denotes Pendred
T591 192-200 NN denotes syndrome
T592 200-201 . denotes .
T770 214-221 NNP denotes Pendred
T771 222-230 NN denotes syndrome
T772 231-233 VBZ denotes is
T773 234-235 DT denotes a
T775 236-246 RB denotes relatively
T776 247-253 JJ denotes common
T777 254-263 JJ denotes autosomal
T779 263-264 HYPH denotes -
T778 264-273 JJ denotes recessive
T774 274-282 NN denotes disorder
R295 T560 T561 nsubj observations,demonstrate
R296 T562 T563 mark that,leads
R297 T563 T561 ccomp leads,demonstrate
R298 T564 T565 compound pendrin,dysfunction
R299 T565 T563 nsubj dysfunction,leads
R300 T566 T563 prep to,leads
R301 T567 T568 det a,loss
R302 T568 T566 pobj loss,to
R303 T569 T568 prep of,loss
R304 T570 T571 compound KCNJ10,expression
R305 T571 T569 pobj expression,of
R306 T572 T571 compound protein,expression
R307 T573 T568 cc and,loss
R308 T574 T575 det a,loss
R309 T575 T568 conj loss,loss
R310 T576 T575 prep of,loss
R311 T577 T578 det the,potential
R312 T578 T576 pobj potential,of
R313 T579 T578 amod endocochlear,potential
R314 T580 T575 punct ", ",loss
R315 T581 T582 dep which,be
R316 T582 T575 relcl be,loss
R317 T583 T582 aux may,be
R318 T584 T585 det the,cause
R319 T585 T582 attr cause,be
R320 T586 T585 amod direct,cause
R321 T587 T585 prep of,cause
R322 T588 T587 pobj deafness,of
R323 T589 T585 prep in,cause
R324 T590 T591 compound Pendred,syndrome
R325 T591 T589 pobj syndrome,in
R326 T592 T561 punct .,demonstrate
R332 T770 T771 compound Pendred,syndrome
R333 T771 T772 nsubj syndrome,is
R334 T773 T774 det a,disorder
R335 T774 T772 attr disorder,is
R336 T775 T776 advmod relatively,common
R337 T776 T774 amod common,disorder
R338 T777 T778 amod autosomal,recessive
R339 T778 T774 amod recessive,disorder
R340 T779 T778 punct -,recessive