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PMC:48141 / 467-1107 JSONTXT

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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
T365 33-38 NCBITaxon:10088 denotes mouse
T366 142-147 GO:0007568 denotes aging
T367 222-236 GO:0007623 denotes diurnal rhythm
T368 323-329 SO:0001023 denotes allele
T369 359-363 SO:0000704 denotes gene
T370 448-452 SO:0000704 denotes gene
T371 537-541 NCBITaxon:10088 denotes mice
T372 617-626 CHEBI:26130 denotes pigmented

craft-sa-dev

Id Subject Object Predicate Lexical cue
T115 0-7 NNS denotes Results
T116 7-100 sentence denotes Based on over 30 studied mouse strains, average IOP ranges from approximately 10 to 20 mmHg.
T117 8-13 VBN denotes Based
T118 60-66 VBZ denotes ranges
T119 14-16 IN denotes on
T120 17-21 IN denotes over
T121 22-24 CD denotes 30
T122 39-46 NNS denotes strains
T123 25-32 VBN denotes studied
T124 33-38 NN denotes mouse
T125 46-48 , denotes ,
T126 48-55 JJ denotes average
T127 56-59 NN denotes IOP
T128 67-71 IN denotes from
T129 72-85 RB denotes approximately
T130 86-88 CD denotes 10
T131 89-91 IN denotes to
T132 92-94 CD denotes 20
T133 95-99 NN denotes mmHg
T134 99-100 . denotes .
T135 100-191 sentence denotes Gender does not typically affect IOP and aging results in an IOP decrease in some strains.
T136 101-107 NN denotes Gender
T137 127-133 VB denotes affect
T138 108-112 VBZ denotes does
T139 113-116 RB denotes not
T140 117-126 RB denotes typically
T141 134-137 NN denotes IOP
T142 138-141 CC denotes and
T143 142-147 NN denotes aging
T144 148-155 VBZ denotes results
T145 156-158 IN denotes in
T146 159-161 DT denotes an
T147 166-174 NN denotes decrease
T148 162-165 NN denotes IOP
T149 175-177 IN denotes in
T150 178-182 DT denotes some
T151 183-190 NNS denotes strains
T152 190-191 . denotes .
T153 191-298 sentence denotes Most tested strains exhibit a diurnal rhythm with IOP being the highest during the dark period of the day.
T154 192-196 JJS denotes Most
T155 204-211 NNS denotes strains
T156 197-203 JJ denotes tested
T157 212-219 VBP denotes exhibit
T158 220-221 DT denotes a
T159 230-236 NN denotes rhythm
T160 222-229 JJ denotes diurnal
T161 237-241 IN denotes with
T162 242-245 NN denotes IOP
T163 246-251 VBG denotes being
T164 252-255 DT denotes the
T165 256-263 JJS denotes highest
T166 264-270 IN denotes during
T167 271-274 DT denotes the
T168 280-286 NN denotes period
T169 275-279 JJ denotes dark
T170 287-289 IN denotes of
T171 290-293 DT denotes the
T172 294-297 NN denotes day
T173 297-298 . denotes .
T174 298-520 sentence denotes Homozygosity for a null allele of the carbonic anhydrase II gene (Car2n) does not alter IOP while homozygosity for a mutation in the leptin receptor gene (Leprdb) that causes obesity and diabetes results in increased IOP.
T175 299-311 NN denotes Homozygosity
T176 381-386 VB denotes alter
T177 312-315 IN denotes for
T178 316-317 DT denotes a
T179 323-329 NN denotes allele
T180 318-322 JJ denotes null
T181 330-332 IN denotes of
T182 333-336 DT denotes the
T183 359-363 NN denotes gene
T184 337-345 JJ denotes carbonic
T185 346-355 NN denotes anhydrase
T186 356-358 CD denotes II
T187 364-365 -LRB- denotes (
T188 365-370 NN denotes Car2n
T189 370-371 -RRB- denotes )
T190 372-376 VBZ denotes does
T191 377-380 RB denotes not
T192 387-390 NN denotes IOP
T193 391-396 IN denotes while
T194 495-502 VBZ denotes results
T195 397-409 NN denotes homozygosity
T196 410-413 IN denotes for
T197 414-415 DT denotes a
T198 416-424 NN denotes mutation
T199 425-427 IN denotes in
T200 428-431 DT denotes the
T201 448-452 NN denotes gene
T202 432-438 NN denotes leptin
T203 439-447 NN denotes receptor
T204 453-454 -LRB- denotes (
T205 454-460 NN denotes Leprdb
T206 460-461 -RRB- denotes )
T207 462-466 WDT denotes that
T208 467-473 VBZ denotes causes
T209 474-481 NN denotes obesity
T210 482-485 CC denotes and
T211 486-494 NN denotes diabetes
T212 503-505 IN denotes in
T213 506-515 VBN denotes increased
T214 516-519 NN denotes IOP
T215 519-520 . denotes .
T216 520-640 sentence denotes Albino C57BL/6J mice homozygous for a tyrosinase mutation (Tyrc-2J) have higher IOPs than their pigmented counterparts.
T217 521-527 NN denotes Albino
T218 537-541 NNS denotes mice
T219 528-533 NN denotes C57BL
T220 534-536 NN denotes 6J
T221 533-534 HYPH denotes /
T222 589-593 VBP denotes have
T223 542-552 JJ denotes homozygous
T224 553-556 IN denotes for
T225 557-558 DT denotes a
T226 570-578 NN denotes mutation
T227 559-569 NN denotes tyrosinase
T228 579-580 -LRB- denotes (
T229 580-584 NN denotes Tyrc
T230 585-587 NN denotes 2J
T231 584-585 HYPH denotes -
T232 587-588 -RRB- denotes )
T233 594-600 JJR denotes higher
T234 601-605 NNS denotes IOPs
T235 606-610 IN denotes than
T236 611-616 PRP$ denotes their
T237 627-639 NNS denotes counterparts
T238 617-626 JJ denotes pigmented
T239 639-640 . denotes .
R82 T122 T119 pobj strains,on
R83 T123 T122 amod studied,strains
R84 T124 T122 compound mouse,strains
R105 T147 T145 pobj decrease,in
R106 T148 T147 compound IOP,decrease
R112 T155 T157 nsubj strains,exhibit
R113 T156 T155 amod tested,strains
R115 T159 T157 dobj rhythm,exhibit
R116 T160 T159 amod diurnal,rhythm
R124 T168 T166 pobj period,during
R125 T169 T168 amod dark,period
R133 T179 T177 pobj allele,for
R134 T180 T179 amod null,allele
R137 T183 T181 pobj gene,of
R138 T184 T183 amod carbonic,gene
R139 T185 T183 nmod anhydrase,gene
R140 T186 T183 nummod II,gene
R148 T194 T176 advcl results,alter
R149 T195 T194 nsubj homozygosity,results
R150 T196 T195 prep for,homozygosity
R151 T197 T198 det a,mutation
R152 T198 T196 pobj mutation,for
R153 T199 T198 prep in,mutation
R154 T200 T201 det the,gene
R155 T201 T199 pobj gene,in
R156 T202 T201 compound leptin,gene
R157 T203 T201 compound receptor,gene
R158 T204 T201 punct (,gene
R159 T205 T201 appos Leprdb,gene
R160 T206 T198 punct ),mutation
R161 T207 T208 dep that,causes
R162 T208 T198 relcl causes,mutation
R163 T209 T208 dobj obesity,causes
R164 T210 T209 cc and,obesity
R165 T211 T209 conj diabetes,obesity
R171 T218 T222 nsubj mice,have
R172 T219 T220 compound C57BL,6J
R174 T221 T220 punct /,6J
R178 T226 T224 pobj mutation,for
R179 T227 T226 compound tyrosinase,mutation
R182 T230 T226 appos 2J,mutation
R183 T231 T230 punct -,2J
R189 T237 T235 pobj counterparts,than
R190 T238 T237 amod pigmented,counterparts
R78 T117 T118 prep Based,ranges
R79 T119 T117 prep on,Based
R80 T120 T121 quantmod over,30
R81 T121 T122 nummod 30,strains
R85 T125 T118 punct ", ",ranges
R86 T126 T127 amod average,IOP
R87 T127 T118 nsubj IOP,ranges
R88 T128 T118 prep from,ranges
R89 T129 T130 advmod approximately,10
R90 T130 T128 pobj 10,from
R91 T131 T128 prep to,from
R92 T132 T131 pobj 20,to
R93 T133 T128 pobj mmHg,from
R94 T134 T118 punct .,ranges
R95 T136 T137 nsubj Gender,affect
R96 T138 T137 aux does,affect
R97 T139 T137 neg not,affect
R98 T140 T137 advmod typically,affect
R99 T141 T137 dobj IOP,affect
R100 T142 T137 cc and,affect
R101 T143 T144 nsubj aging,results
R102 T144 T137 conj results,affect
R103 T145 T144 prep in,results
R104 T146 T147 det an,decrease
R107 T149 T144 prep in,results
R108 T150 T151 det some,strains
R109 T151 T149 pobj strains,in
R110 T152 T144 punct .,results
R111 T154 T155 amod Most,strains
R114 T158 T159 det a,rhythm
R117 T161 T157 prep with,exhibit
R118 T162 T163 nsubj IOP,being
R119 T163 T161 pcomp being,with
R120 T164 T165 advmod the,highest
R121 T165 T163 acomp highest,being
R122 T166 T163 prep during,being
R123 T167 T168 det the,period
R126 T170 T168 prep of,period
R127 T171 T172 det the,day
R128 T172 T170 pobj day,of
R129 T173 T157 punct .,exhibit
R130 T175 T176 nsubj Homozygosity,alter
R131 T177 T175 prep for,Homozygosity
R132 T178 T179 det a,allele
R135 T181 T179 prep of,allele
R136 T182 T183 det the,gene
R141 T187 T183 punct (,gene
R142 T188 T183 appos Car2n,gene
R143 T189 T176 punct ),alter
R144 T190 T176 aux does,alter
R145 T191 T176 neg not,alter
R146 T192 T176 dobj IOP,alter
R147 T193 T194 mark while,results
R166 T212 T194 prep in,results
R167 T213 T214 amod increased,IOP
R168 T214 T212 pobj IOP,in
R169 T215 T176 punct .,alter
R170 T217 T218 compound Albino,mice
R173 T220 T218 compound 6J,mice
R175 T223 T218 amod homozygous,mice
R176 T224 T223 prep for,homozygous
R177 T225 T226 det a,mutation
R180 T228 T226 punct (,mutation
R181 T229 T230 compound Tyrc,2J
R184 T232 T222 punct ),have
R185 T233 T234 amod higher,IOPs
R186 T234 T222 dobj IOPs,have
R187 T235 T234 prep than,IOPs
R188 T236 T237 poss their,counterparts
R191 T239 T222 punct .,have

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
T394 33-38 NCBITaxon:10088 denotes mouse
T395 142-147 GO:0007568 denotes aging
T396 222-236 GO:0007623 denotes diurnal rhythm
T397 318-322 SO_EXT:sequence_nullness denotes null
T398 323-329 SO_EXT:0001023 denotes allele
T399 337-355 GO_EXT:0004089 denotes carbonic anhydrase
T400 337-358 PR_EXT:carbonic_anhydrase_2 denotes carbonic anhydrase II
T401 359-363 SO_EXT:0000704 denotes gene
T402 365-369 PR_EXT:carbonic_anhydrase_2 denotes Car2
T403 416-424 SO_EXT:sequence_alteration_entity_or_process denotes mutation
T404 432-438 CHEBI_PR_EXT:leptin denotes leptin
T405 432-447 GO_PR_EXT:leptin_receptor denotes leptin receptor
T406 448-452 SO_EXT:0000704 denotes gene
T407 454-458 GO_PR_EXT:leptin_receptor denotes Lepr
T408 537-541 NCBITaxon:10088 denotes mice
T409 559-569 GO_PR_EXT:monophenol_monooxygenase_or_tyrosinase denotes tyrosinase
T410 570-578 SO_EXT:sequence_alteration_entity_or_process denotes mutation
T411 580-583 GO_PR_EXT:monophenol_monooxygenase_or_tyrosinase denotes Tyr
T412 617-626 CHEBI_EXT:26130 denotes pigmented