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PMC:548520 / 118-502 JSONTXT

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craft-ca-core-ex-dev

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

Id Subject Object Predicate Lexical cue
T76 48-59 NCBITaxon:1 denotes individuals
T77 90-95 GO:0007567 denotes birth
T79 132-146,158-164 GO:0060041 denotes development of retina
T80 151-164 UBERON:0003902 denotes neural retina
T81 166-175 SO_EXT:sequence_alteration_entity_or_process denotes Mutations
T82 179-184 SO_EXT:0000704 denotes genes
T84 201-212,229-251 GO:0042461 denotes development of photoreceptor cells
T85 232-251 CL:0000210 denotes photoreceptor cells
T86 246-251 CL_GO_EXT:cell denotes cells
T87 327-336 SO_EXT:sequence_alteration_entity_or_process denotes mutations
T88 344-357 CL:0000210 denotes photoreceptor
T89 358-371 GO_EXT:transcription denotes transcription
T90 358-378 GO_EXT:transcription_factor denotes transcription factor
T91 380-383 PR_EXT:000005904 denotes Crx

craft-ca-core-dev

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

Id Subject Object Predicate Lexical cue
T41 48-59 NCBITaxon:1 denotes individuals
T42 90-95 GO:0007567 denotes birth
T44 132-146,158-164 GO:0060041 denotes development of retina
T45 151-164 UBERON:0003902 denotes neural retina
T46 179-184 SO:0000704 denotes genes
T48 201-212,229-251 GO:0042461 denotes development of photoreceptor cells
T49 232-251 CL:0000210 denotes photoreceptor cells
T50 344-357 CL:0000210 denotes photoreceptor
T51 380-383 PR:000005904 denotes Crx

craft-sa-dev

Id Subject Object Predicate Lexical cue
T135 0-2 IN denotes In
T136 60-63 VBP denotes are
T137 3-8 NNP denotes Leber
T138 22-31 NN denotes amaurosis
T139 8-10 POS denotes 's
T140 11-21 JJ denotes congenital
T141 32-33 -LRB- denotes (
T142 33-36 NN denotes LCA
T143 36-37 -RRB- denotes )
T144 37-39 , denotes ,
T145 39-47 VBN denotes affected
T146 48-59 NNS denotes individuals
T147 64-69 JJ denotes blind
T148 69-71 , denotes ,
T149 71-73 CC denotes or
T150 74-80 RB denotes nearly
T151 81-83 RB denotes so
T152 83-85 , denotes ,
T153 85-89 IN denotes from
T154 90-95 NN denotes birth
T155 95-96 . denotes .
T156 96-165 sentence denotes This early onset suggests abnormal development of the neural retina.
T157 97-101 DT denotes This
T158 108-113 NN denotes onset
T159 102-107 JJ denotes early
T160 114-122 VBZ denotes suggests
T161 123-131 JJ denotes abnormal
T162 132-143 NN denotes development
T163 144-146 IN denotes of
T164 147-150 DT denotes the
T165 158-164 NN denotes retina
T166 151-157 JJ denotes neural
T167 164-165 . denotes .
T168 165-303 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 166-175 NNS denotes Mutations
T170 262-267 VBN denotes found
T171 176-178 IN denotes in
T172 179-184 NNS denotes genes
T173 185-189 WDT denotes that
T174 190-196 VBP denotes affect
T175 197-200 DT denotes the
T176 201-212 NN denotes development
T177 213-216 CC denotes and
T178 216-217 HYPH denotes /
T179 217-219 CC denotes or
T180 220-228 NN denotes function
T181 229-231 IN denotes of
T182 232-245 NN denotes photoreceptor
T183 246-251 NNS denotes cells
T184 252-256 VBP denotes have
T185 257-261 VBN denotes been
T186 268-270 TO denotes to
T187 271-273 VB denotes be
T188 274-285 JJ denotes responsible
T189 286-288 IN denotes in
T190 289-293 DT denotes some
T191 294-302 NNS denotes families
T192 302-303 . denotes .
T193 303-384 sentence denotes These examples include mutations in the photoreceptor transcription factor, Crx.
T194 304-309 DT denotes These
T195 310-318 NNS denotes examples
T196 319-326 VBP denotes include
T197 327-336 NNS denotes mutations
T198 337-339 IN denotes in
T199 340-343 DT denotes the
T200 372-378 NN denotes factor
T201 344-357 NN denotes photoreceptor
T202 358-371 NN denotes transcription
T203 378-380 , denotes ,
T204 380-383 NN denotes Crx
T205 383-384 . 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