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PMC:1183529 / 20516-20687 JSONTXT 3 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue
T10346 4-11 NNS denotes domains
T10347 12-13 -LRB- denotes (
T10348 13-19 NN denotes Figure
T10349 20-21 CD denotes 7
T10350 21-22 -RRB- denotes )
T10351 22-23 . denotes .
T10352 23-103 sentence denotes This base change was not present in the analysis of DNA from 400 normal adults.
T10353 24-28 DT denotes This
T10355 29-33 NN denotes base
T10354 34-40 NN denotes change
T10356 41-44 VBD denotes was
T10357 45-48 RB denotes not
T10358 49-56 JJ denotes present
T10359 57-59 IN denotes in
T10360 60-63 DT denotes the
T10361 64-72 NN denotes analysis
T10362 73-75 IN denotes of
T10363 76-79 NN denotes DNA
T10364 80-84 IN denotes from
T10365 85-88 CD denotes 400
T10367 89-95 JJ denotes normal
T10366 96-102 NNS denotes adults
T10368 102-103 . denotes .
T10370 104-106 TO denotes To
T10371 107-113 VB denotes assess
T10373 114-117 DT denotes the
T10374 118-128 NN denotes likelihood
T10375 129-133 IN denotes that
T10377 134-137 DT denotes the
T10378 138-146 NN denotes mutation
T10376 147-150 VBD denotes was
T10379 151-157 JJ denotes causal
T10380 158-161 IN denotes for
T10381 162-165 DT denotes the
R2927 T10347 T10348 punct (,Figure
R2929 T10349 T10348 nummod 7,Figure
R2930 T10350 T10348 punct ),Figure
R2932 T10353 T10354 det This,change
R2933 T10354 T10356 nsubj change,was
R2934 T10355 T10354 compound base,change
R2935 T10357 T10356 neg not,was
R2936 T10358 T10356 acomp present,was
R2937 T10359 T10356 prep in,was
R2938 T10360 T10361 det the,analysis
R2939 T10361 T10359 pobj analysis,in
R2940 T10362 T10361 prep of,analysis
R2941 T10363 T10362 pobj DNA,of
R2942 T10364 T10363 prep from,DNA
R2943 T10365 T10366 nummod 400,adults
R2944 T10366 T10364 pobj adults,from
R2945 T10367 T10366 amod normal,adults
R2946 T10368 T10356 punct .,was
R2947 T10370 T10371 aux To,assess
R2949 T10373 T10374 det the,likelihood
R2950 T10374 T10371 dobj likelihood,assess
R2951 T10375 T10376 mark that,was
R2952 T10376 T10374 acl was,likelihood
R2953 T10377 T10378 det the,mutation
R2954 T10378 T10376 nsubj mutation,was
R2955 T10379 T10376 acomp causal,was
R2956 T10380 T10379 prep for,causal