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PMC:1186732 / 419-652 JSONTXT 4 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue
T247 7-10 DT denotes the
T249 11-24 NN denotes photoreceptor
T248 25-30 NNS denotes cells
T250 31-33 IN denotes of
T251 34-37 DT denotes the
T253 38-45 JJ denotes retinal
T254 46-58 NN denotes degeneration
T255 59-60 CD denotes 7
T256 61-62 -LRB- denotes (
T257 62-65 NN denotes rd7
T258 65-66 -RRB- denotes )
T259 67-73 NN denotes mutant
T252 74-79 NN denotes mouse
T260 79-81 , denotes ,
T261 81-82 DT denotes a
T262 83-88 NN denotes model
T263 89-92 IN denotes for
T264 93-96 DT denotes the
T266 97-102 JJ denotes human
T267 103-111 VBN denotes enhanced
T268 112-113 NN denotes S
T270 113-114 HYPH denotes -
T269 114-118 NN denotes cone
T265 119-127 NN denotes syndrome
T271 128-129 -LRB- denotes (
T272 129-133 NN denotes ESCS
T273 133-134 -RRB- denotes )
T274 134-135 . denotes .
T276 136-140 DT denotes This
T277 141-147 NN denotes mutant
T278 148-155 VBZ denotes carries
T279 156-157 DT denotes a
T281 158-169 JJ denotes spontaneous
T280 170-178 NN denotes deletion
T282 179-181 IN denotes in
T283 182-185 DT denotes the
T285 186-191 NN denotes mouse
T284 192-200 NN denotes ortholog
T286 201-203 IN denotes of
T287 204-209 NN denotes NR2E3
T288 209-211 , denotes ,
T289 211-213 DT denotes an
T291 214-220 NN denotes orphan
T292 221-228 JJ denotes nuclear
R100 T286 T284 prep of,ortholog
R101 T287 T286 pobj NR2E3,of
R102 T288 T287 punct ", ",NR2E3
R63 T247 T248 det the,cells
R65 T249 T248 compound photoreceptor,cells
R66 T250 T248 prep of,cells
R67 T251 T252 det the,mouse
R68 T252 T250 pobj mouse,of
R69 T253 T254 amod retinal,degeneration
R70 T254 T252 nmod degeneration,mouse
R71 T255 T254 nummod 7,degeneration
R72 T256 T254 punct (,degeneration
R73 T257 T254 appos rd7,degeneration
R74 T258 T252 punct ),mouse
R75 T259 T252 compound mutant,mouse
R76 T260 T252 punct ", ",mouse
R77 T261 T262 det a,model
R78 T262 T252 appos model,mouse
R79 T263 T262 prep for,model
R80 T264 T265 det the,syndrome
R81 T265 T263 pobj syndrome,for
R82 T266 T265 amod human,syndrome
R83 T267 T265 amod enhanced,syndrome
R84 T268 T269 compound S,cone
R85 T269 T265 compound cone,syndrome
R86 T270 T269 punct -,cone
R87 T271 T265 punct (,syndrome
R88 T272 T265 appos ESCS,syndrome
R91 T276 T277 det This,mutant
R92 T277 T278 nsubj mutant,carries
R93 T279 T280 det a,deletion
R94 T280 T278 dobj deletion,carries
R95 T281 T280 amod spontaneous,deletion
R96 T282 T280 prep in,deletion
R97 T283 T284 det the,ortholog
R98 T284 T282 pobj ortholog,in
R99 T285 T284 compound mouse,ortholog