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PMC:539297 / 180-316 JSONTXT 4 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function

Id Subject Object Predicate Lexical cue
T196 1-2 DT denotes a
T198 3-14 RB denotes recessively
T199 15-24 VBN denotes inherited
T200 24-26 , denotes ,
T201 26-35 NN denotes childhood
T203 35-36 HYPH denotes -
T202 36-41 NN denotes onset
T204 42-59 JJ denotes neurodegenerative
T197 60-67 NN denotes disease
T205 68-72 RBS denotes most
T207 72-73 HYPH denotes -
T206 73-81 RB denotes commonly
T208 82-88 VBN denotes caused
T209 89-91 IN denotes by
T210 92-93 DT denotes a
T212 94-95 SYM denotes ~
T213 95-96 CD denotes 1
T214 97-99 NN denotes kb
T215 100-104 NN denotes CLN3
T211 105-113 NN denotes mutation
T216 113-114 . denotes .
T218 115-118 DT denotes The
T220 119-128 JJ denotes resulting
T219 129-133 NN denotes loss
T222 134-136 IN denotes of
R21 T196 T197 det a,disease
R23 T198 T199 advmod recessively,inherited
R24 T199 T197 amod inherited,disease
R25 T200 T197 punct ", ",disease
R26 T201 T202 nmod childhood,onset
R27 T202 T197 nmod onset,disease
R28 T203 T202 punct -,onset
R29 T204 T197 amod neurodegenerative,disease
R30 T205 T206 advmod most,commonly
R31 T206 T208 advmod commonly,caused
R32 T207 T206 punct -,commonly
R33 T208 T197 acl caused,disease
R34 T209 T208 agent by,caused
R35 T210 T211 det a,mutation
R36 T211 T209 pobj mutation,by
R37 T212 T213 punct ~,1
R38 T213 T214 nummod 1,kb
R39 T214 T211 compound kb,mutation
R40 T215 T211 compound CLN3,mutation
R42 T218 T219 det The,loss
R44 T220 T219 amod resulting,loss
R45 T222 T219 prep of,loss