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PMC:548520 / 107-502 JSONTXT

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craft-ca-core-ex-dev

Below, discontinuous spans are shown in the chain model. You can change it to the bag model.

Id Subject Object Predicate Lexical cue
T76 59-70 NCBITaxon:1 denotes individuals
T77 101-106 GO:0007567 denotes birth
T78 143-157 _FRAGMENT denotes development of
T79 169-175 GO:0060041 denotes retina
T80 162-175 UBERON:0003902 denotes neural retina
T81 177-186 SO_EXT:sequence_alteration_entity_or_process denotes Mutations
T82 190-195 SO_EXT:0000704 denotes genes
T83 212-223 _FRAGMENT denotes development
T84 240-262 GO:0042461 denotes of photoreceptor cells
T85 243-262 CL:0000210 denotes photoreceptor cells
T86 257-262 CL_GO_EXT:cell denotes cells
T87 338-347 SO_EXT:sequence_alteration_entity_or_process denotes mutations
T88 355-368 CL:0000210 denotes photoreceptor
T89 369-382 GO_EXT:transcription denotes transcription
T90 369-389 GO_EXT:transcription_factor denotes transcription factor
T91 391-394 PR_EXT:000005904 denotes Crx
R3 T79 T78 _lexicallyChainedTo retina,development of
R4 T84 T83 _lexicallyChainedTo of photoreceptor cells,development

craft-ca-core-dev

Below, discontinuous spans are shown in the chain model. You can change it to the bag model.

Id Subject Object Predicate Lexical cue
T41 59-70 NCBITaxon:1 denotes individuals
T42 101-106 GO:0007567 denotes birth
T43 143-157 _FRAGMENT denotes development of
T44 169-175 GO:0060041 denotes retina
T45 162-175 UBERON:0003902 denotes neural retina
T46 190-195 SO:0000704 denotes genes
T47 212-223 _FRAGMENT denotes development
T48 240-262 GO:0042461 denotes of photoreceptor cells
T49 243-262 CL:0000210 denotes photoreceptor cells
T50 355-368 CL:0000210 denotes photoreceptor
T51 391-394 PR:000005904 denotes Crx
R1 T44 T43 _lexicallyChainedTo retina,development of
R2 T48 T47 _lexicallyChainedTo of photoreceptor cells,development

craft-sa-dev

Id Subject Object Predicate Lexical cue
T132 0-10 sentence denotes Background
T133 0-10 NN denotes Background
T134 10-107 sentence denotes In Leber's congenital amaurosis (LCA), affected individuals are blind, or nearly so, from birth.
T135 11-13 IN denotes In
T136 71-74 VBP denotes are
T137 14-19 NNP denotes Leber
T138 33-42 NN denotes amaurosis
T139 19-21 POS denotes 's
T140 22-32 JJ denotes congenital
T141 43-44 -LRB- denotes (
T142 44-47 NN denotes LCA
T143 47-48 -RRB- denotes )
T144 48-50 , denotes ,
T145 50-58 VBN denotes affected
T146 59-70 NNS denotes individuals
T147 75-80 JJ denotes blind
T148 80-82 , denotes ,
T149 82-84 CC denotes or
T150 85-91 RB denotes nearly
T151 92-94 RB denotes so
T152 94-96 , denotes ,
T153 96-100 IN denotes from
T154 101-106 NN denotes birth
T155 106-107 . denotes .
T156 107-176 sentence denotes This early onset suggests abnormal development of the neural retina.
T157 108-112 DT denotes This
T158 119-124 NN denotes onset
T159 113-118 JJ denotes early
T160 125-133 VBZ denotes suggests
T161 134-142 JJ denotes abnormal
T162 143-154 NN denotes development
T163 155-157 IN denotes of
T164 158-161 DT denotes the
T165 169-175 NN denotes retina
T166 162-168 JJ denotes neural
T167 175-176 . denotes .
T168 176-314 sentence denotes Mutations in genes that affect the development and/or function of photoreceptor cells have been found to be responsible in some families.
T169 177-186 NNS denotes Mutations
T170 273-278 VBN denotes found
T171 187-189 IN denotes in
T172 190-195 NNS denotes genes
T173 196-200 WDT denotes that
T174 201-207 VBP denotes affect
T175 208-211 DT denotes the
T176 212-223 NN denotes development
T177 224-227 CC denotes and
T178 227-228 HYPH denotes /
T179 228-230 CC denotes or
T180 231-239 NN denotes function
T181 240-242 IN denotes of
T182 243-256 NN denotes photoreceptor
T183 257-262 NNS denotes cells
T184 263-267 VBP denotes have
T185 268-272 VBN denotes been
T186 279-281 TO denotes to
T187 282-284 VB denotes be
T188 285-296 JJ denotes responsible
T189 297-299 IN denotes in
T190 300-304 DT denotes some
T191 305-313 NNS denotes families
T192 313-314 . denotes .
T193 314-395 sentence denotes These examples include mutations in the photoreceptor transcription factor, Crx.
T194 315-320 DT denotes These
T195 321-329 NNS denotes examples
T196 330-337 VBP denotes include
T197 338-347 NNS denotes mutations
T198 348-350 IN denotes in
T199 351-354 DT denotes the
T200 383-389 NN denotes factor
T201 355-368 NN denotes photoreceptor
T202 369-382 NN denotes transcription
T203 389-391 , denotes ,
T204 391-394 NN denotes Crx
T205 394-395 . denotes .
R18 T135 T136 prep In,are
R19 T137 T138 poss Leber,amaurosis
R20 T138 T135 pobj amaurosis,In
R21 T139 T137 case 's,Leber
R22 T140 T138 amod congenital,amaurosis
R23 T141 T138 punct (,amaurosis
R24 T142 T138 appos LCA,amaurosis
R25 T143 T136 punct ),are
R26 T144 T136 punct ", ",are
R27 T145 T146 amod affected,individuals
R28 T146 T136 nsubj individuals,are
R29 T147 T136 acomp blind,are
R30 T148 T147 punct ", ",blind
R31 T149 T147 cc or,blind
R32 T150 T151 advmod nearly,so
R33 T151 T147 conj so,blind
R34 T152 T136 punct ", ",are
R35 T153 T136 prep from,are
R36 T154 T153 pobj birth,from
R37 T155 T136 punct .,are
R38 T157 T158 det This,onset
R39 T158 T160 nsubj onset,suggests
R40 T159 T158 amod early,onset
R41 T161 T162 amod abnormal,development
R42 T162 T160 dobj development,suggests
R43 T163 T162 prep of,development
R44 T164 T165 det the,retina
R45 T165 T163 pobj retina,of
R46 T166 T165 amod neural,retina
R47 T167 T160 punct .,suggests
R48 T169 T170 nsubjpass Mutations,found
R49 T171 T169 prep in,Mutations
R50 T172 T171 pobj genes,in
R51 T173 T174 dep that,affect
R52 T174 T172 relcl affect,genes
R53 T175 T176 det the,development
R54 T176 T174 dobj development,affect
R55 T177 T176 cc and,development
R56 T178 T177 punct /,and
R57 T179 T177 cc or,and
R58 T180 T176 conj function,development
R59 T181 T176 prep of,development
R60 T182 T183 compound photoreceptor,cells
R61 T183 T181 pobj cells,of
R62 T184 T170 aux have,found
R63 T185 T170 auxpass been,found
R64 T186 T187 aux to,be
R65 T187 T170 xcomp be,found
R66 T188 T187 acomp responsible,be
R67 T189 T170 prep in,found
R68 T190 T191 det some,families
R69 T191 T189 pobj families,in
R70 T192 T170 punct .,found
R71 T194 T195 det These,examples
R72 T195 T196 nsubj examples,include
R73 T197 T196 dobj mutations,include
R74 T198 T197 prep in,mutations
R75 T199 T200 det the,factor
R76 T200 T198 pobj factor,in
R77 T201 T202 compound photoreceptor,transcription
R78 T202 T200 compound transcription,factor
R79 T203 T200 punct ", ",factor
R80 T204 T200 appos Crx,factor
R81 T205 T196 punct .,include