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PMC:1189074 / 0-824 JSONTXT

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Id Subject Object Predicate Lexical cue
T78 222-227 JJ denotes fatty
T79 228-232 NN denotes acid
T80 233-234 NN denotes β
T81 234-235 HYPH denotes -
T82 245-247 IN denotes in
T83 248-254 NNS denotes humans
T84 254-255 . denotes .
T85 255-415 sentence denotes To better understand the pathogenesis of this disease, we developed a mouse model for MCAD deficiency (MCAD−/−) by gene targeting in embryonic stem (ES) cells.
T86 256-258 TO denotes To
T87 266-276 VB denotes understand
T88 259-265 RBR denotes better
T89 314-323 VBD denotes developed
T90 277-280 DT denotes the
T91 281-293 NN denotes pathogenesis
T92 294-296 IN denotes of
T93 297-301 DT denotes this
T94 302-309 NN denotes disease
T95 309-311 , denotes ,
T96 311-313 PRP denotes we
T97 324-325 DT denotes a
T98 332-337 NN denotes model
T99 326-331 NN denotes mouse
T100 338-341 IN denotes for
T101 342-346 NN denotes MCAD
T102 347-357 NN denotes deficiency
T103 358-359 -LRB- denotes (
T104 359-363 NN denotes MCAD
T105 363-364 SYM denotes
T106 364-365 HYPH denotes /
T107 365-366 SYM denotes
T108 366-367 -RRB- denotes )
T109 368-370 IN denotes by
T110 371-375 NN denotes gene
T111 376-385 NN denotes targeting
T112 386-388 IN denotes in
T113 389-398 JJ denotes embryonic
T114 399-403 NN denotes stem
T115 409-414 NNS denotes cells
T116 404-405 -LRB- denotes (
T117 405-407 NN denotes ES
T118 407-408 -RRB- denotes )
T119 414-415 . denotes .
T120 415-544 sentence denotes The MCAD−/− mice developed an organic aciduria and fatty liver, and showed profound cold intolerance at 4 °C with prior fasting.
T121 416-419 DT denotes The
T152 609-617 VBN denotes reported
T153 574-578 VBN denotes seen
T154 579-581 IN denotes in
T155 582-586 NN denotes MCAD
T156 590-594 NNS denotes mice
T157 586-587 SYM denotes
T158 587-588 HYPH denotes /
T159 588-589 SYM denotes
T160 595-599 VBP denotes have
T161 600-603 RB denotes not
T162 604-608 VBN denotes been
T163 618-620 IN denotes in
T164 621-626 JJ denotes human
T165 632-640 NNS denotes patients
T166 627-631 NN denotes MCAD
T167 640-641 . denotes .
T168 641-800 sentence denotes There was significant neonatal mortality of MCAD−/− pups demonstrating similarities to patterns of clinical episodes and mortality in MCAD-deficient patients.
T169 642-647 EX denotes There
T170 648-651 VBD denotes was
T171 652-663 JJ denotes significant
T172 673-682 NN denotes mortality
T173 664-672 JJ denotes neonatal
T174 683-685 IN denotes of
T175 686-690 NN denotes MCAD
T176 694-698 NNS denotes pups
T177 690-691 SYM denotes
T178 691-692 HYPH denotes /
T179 692-693 SYM denotes
T180 699-712 VBG denotes demonstrating
T181 713-725 NNS denotes similarities
T182 726-728 IN denotes to
T183 729-737 NNS denotes patterns
T184 738-740 IN denotes of
T185 741-749 JJ denotes clinical
T186 750-758 NNS denotes episodes
T187 759-762 CC denotes and
T188 763-772 NN denotes mortality
T189 773-775 IN denotes in
T190 776-780 NN denotes MCAD
T191 781-790 JJ denotes deficient
T192 780-781 HYPH denotes -
T193 791-799 NNS denotes patients
T194 799-800 . denotes .
T196 801-804 DT denotes The
T198 805-809 NN denotes MCAD
T199 810-819 JJ denotes deficient
T200 809-810 HYPH denotes -
T43 0-6 JJ denotes Medium
T44 7-12 NN denotes Chain
T45 0-68 sentence denotes Medium-Chain Acyl-CoA Dehydrogenase Deficiency in Gene-Targeted Mice
T46 6-7 HYPH denotes -
T47 22-35 NN denotes Dehydrogenase
T48 13-17 NN denotes Acyl
T49 18-21 NN denotes CoA
T50 17-18 HYPH denotes -
T51 36-46 NN denotes Deficiency
T52 47-49 IN denotes in
T53 50-54 NN denotes Gene
T54 55-63 VBN denotes Targeted
T55 54-55 HYPH denotes -
T56 64-68 NNS denotes Mice
T57 68-255 sentence denotes MCAD Gene Disruption in the Mouse Abstract Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency is the most common inherited disorder of mitochondrial fatty acid β-oxidation in humans.
T58 69-119 JJ denotes MCAD Gene Disruption in the Mouse Abstract Medium
T59 120-125 NN denotes chain
T60 119-120 HYPH denotes -
T61 135-148 NN denotes dehydrogenase
T62 126-130 NN denotes acyl
T63 131-134 NN denotes CoA
T64 130-131 HYPH denotes -
T65 156-166 NN denotes deficiency
T66 149-150 -LRB- denotes (
T67 150-154 NN denotes MCAD
T68 154-155 -RRB- denotes )
T69 167-169 VBZ denotes is
T70 170-173 DT denotes the
T71 196-204 NN denotes disorder
T72 174-178 RBS denotes most
T73 179-185 JJ denotes common
T74 186-195 VBN denotes inherited
T75 205-207 IN denotes of
T76 208-221 JJ denotes mitochondrial
T77 235-244 NN denotes oxidation
T122 428-432 NNS denotes mice
T123 420-424 NN denotes MCAD
T124 424-425 SYM denotes
T125 425-426 HYPH denotes /
T126 426-427 SYM denotes
T127 433-442 VBD denotes developed
T128 443-445 DT denotes an
T129 454-462 NN denotes aciduria
T130 446-453 JJ denotes organic
T131 463-466 CC denotes and
T132 467-472 JJ denotes fatty
T133 473-478 NN denotes liver
T134 478-480 , denotes ,
T135 480-483 CC denotes and
T136 484-490 VBD denotes showed
T137 491-499 JJ denotes profound
T138 505-516 NN denotes intolerance
T139 500-504 NN denotes cold
T140 517-519 IN denotes at
T141 520-521 CD denotes 4
T142 522-524 NN denotes °C
T143 525-529 IN denotes with
T144 530-535 JJ denotes prior
T145 536-543 NN denotes fasting
T146 543-544 . denotes .
T147 544-641 sentence denotes The sporadic cardiac lesions seen in MCAD−/− mice have not been reported in human MCAD patients.
T148 545-548 DT denotes The
T149 566-573 NNS denotes lesions
T150 549-557 JJ denotes sporadic
T151 558-565 JJ denotes cardiac
R74 T187 T186 cc and,episodes
R75 T188 T186 conj mortality,episodes
R76 T189 T183 prep in,patterns
R1 T78 T79 amod fatty,acid
R2 T79 T77 compound acid,oxidation
R3 T80 T77 compound β,oxidation
R4 T81 T77 punct -,oxidation
R5 T82 T69 prep in,is
R6 T83 T82 pobj humans,in
R7 T84 T69 punct .,is
R8 T86 T87 aux To,understand
R9 T87 T89 advcl understand,developed
R10 T88 T87 advmod better,understand
R11 T90 T91 det the,pathogenesis
R12 T91 T87 dobj pathogenesis,understand
R13 T92 T91 prep of,pathogenesis
R14 T93 T94 det this,disease
R15 T94 T92 pobj disease,of
R16 T95 T89 punct ", ",developed
R17 T96 T89 nsubj we,developed
R18 T97 T98 det a,model
R19 T98 T89 dobj model,developed
R20 T99 T98 compound mouse,model
R21 T100 T98 prep for,model
R22 T101 T102 compound MCAD,deficiency
R23 T102 T100 pobj deficiency,for
R24 T103 T102 punct (,deficiency
R25 T104 T102 appos MCAD,deficiency
R26 T105 T104 punct −,MCAD
R27 T106 T104 punct /,MCAD
R28 T107 T104 punct −,MCAD
R29 T108 T89 punct ),developed
R30 T109 T89 prep by,developed
R31 T110 T111 compound gene,targeting
R32 T111 T109 pobj targeting,by
R33 T112 T111 prep in,targeting
R34 T113 T114 amod embryonic,stem
R35 T114 T115 nmod stem,cells
R36 T115 T112 pobj cells,in
R37 T116 T114 punct (,stem
R38 T117 T114 appos ES,stem
R39 T118 T115 punct ),cells
R40 T119 T89 punct .,developed
R41 T121 T122 det The,mice
R42 T153 T149 acl seen,lesions
R43 T154 T153 prep in,seen
R44 T155 T156 nmod MCAD,mice
R45 T156 T154 pobj mice,in
R46 T157 T155 punct −,MCAD
R47 T158 T155 punct /,MCAD
R48 T159 T155 punct −,MCAD
R49 T160 T152 aux have,reported
R50 T161 T152 neg not,reported
R51 T162 T152 auxpass been,reported
R52 T163 T152 prep in,reported
R53 T164 T165 amod human,patients
R54 T165 T163 pobj patients,in
R55 T166 T165 compound MCAD,patients
R56 T167 T152 punct .,reported
R57 T169 T170 expl There,was
R58 T171 T172 amod significant,mortality
R59 T172 T170 attr mortality,was
R60 T173 T172 amod neonatal,mortality
R61 T174 T172 prep of,mortality
R62 T175 T176 nmod MCAD,pups
R63 T176 T174 pobj pups,of
R64 T177 T175 punct −,MCAD
R65 T178 T175 punct /,MCAD
R66 T179 T175 punct −,MCAD
R67 T180 T172 acl demonstrating,mortality
R68 T181 T180 dobj similarities,demonstrating
R69 T182 T181 prep to,similarities
R70 T183 T182 pobj patterns,to
R71 T184 T183 prep of,patterns
R72 T185 T186 amod clinical,episodes
R73 T186 T184 pobj episodes,of
R77 T190 T191 npadvmod MCAD,deficient
R78 T191 T193 amod deficient,patients
R79 T192 T191 punct -,deficient
R80 T193 T189 pobj patients,in
R81 T194 T170 punct .,was
R84 T198 T199 npadvmod MCAD,deficient
R86 T200 T199 punct -,deficient
R122 T43 T44 amod Medium,Chain
R123 T44 T47 compound Chain,Dehydrogenase
R124 T46 T44 punct -,Chain
R125 T47 T51 compound Dehydrogenase,Deficiency
R126 T48 T49 compound Acyl,CoA
R127 T49 T47 compound CoA,Dehydrogenase
R128 T50 T49 punct -,CoA
R129 T52 T51 prep in,Deficiency
R130 T53 T54 npadvmod Gene,Targeted
R131 T54 T56 amod Targeted,Mice
R132 T55 T54 punct -,Targeted
R133 T56 T52 pobj Mice,in
R134 T58 T59 amod "MCAD Gene Disruption in the Mouse Abstract Medium",chain
R135 T59 T61 nmod chain,dehydrogenase
R136 T60 T59 punct -,chain
R137 T61 T65 nmod dehydrogenase,deficiency
R138 T62 T63 nmod acyl,CoA
R139 T63 T61 nmod CoA,dehydrogenase
R140 T64 T63 punct -,CoA
R141 T65 T69 nsubj deficiency,is
R142 T66 T61 punct (,dehydrogenase
R143 T67 T61 appos MCAD,dehydrogenase
R144 T68 T65 punct ),deficiency
R145 T70 T71 det the,disorder
R146 T71 T69 attr disorder,is
R147 T72 T73 advmod most,common
R148 T73 T71 amod common,disorder
R149 T74 T71 amod inherited,disorder
R150 T75 T71 prep of,disorder
R151 T76 T77 amod mitochondrial,oxidation
R152 T77 T75 pobj oxidation,of
R153 T122 T127 nsubj mice,developed
R154 T123 T122 nmod MCAD,mice
R155 T124 T123 punct −,MCAD
R156 T125 T123 punct /,MCAD
R157 T126 T123 punct −,MCAD
R158 T128 T129 det an,aciduria
R159 T129 T127 dobj aciduria,developed
R160 T130 T129 amod organic,aciduria
R161 T131 T129 cc and,aciduria
R162 T132 T133 amod fatty,liver
R163 T133 T129 conj liver,aciduria
R164 T134 T127 punct ", ",developed
R165 T135 T127 cc and,developed
R166 T136 T127 conj showed,developed
R167 T137 T138 amod profound,intolerance
R168 T138 T136 dobj intolerance,showed
R169 T139 T138 compound cold,intolerance
R170 T140 T136 prep at,showed
R171 T141 T142 nummod 4,°C
R172 T142 T140 pobj °C,at
R173 T143 T136 prep with,showed
R174 T144 T145 amod prior,fasting
R175 T145 T143 pobj fasting,with
R176 T146 T127 punct .,developed
R177 T148 T149 det The,lesions
R178 T149 T152 nsubjpass lesions,reported
R179 T150 T149 amod sporadic,lesions
R180 T151 T149 amod cardiac,lesions

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
T242 326-331 NCBITaxon:10088 denotes mouse
T243 371-375 SO:0000704 denotes gene
T244 389-398 UBERON:0000922 denotes embryonic
T245 389-403 _FRAGMENT denotes embryonic stem
T246 409-414 CL:0002322 denotes cells
T247 405-407 _FRAGMENT denotes ES
T248 428-432 NCBITaxon:10088 denotes mice
T249 473-478 UBERON:0002107 denotes liver
T250 558-565 UBERON:0000948 denotes cardiac
T251 590-594 NCBITaxon:10088 denotes mice
T252 621-626 NCBITaxon:9606 denotes human
T233 0-21 CHEBI:61907 denotes Medium-Chain Acyl-CoA
T234 50-54 SO:0000704 denotes Gene
T235 64-68 NCBITaxon:10088 denotes Mice
T236 69-134 CHEBI:61907 denotes MCAD Gene Disruption in the Mouse Abstract Medium-chain acyl-CoA
T237 208-221 GO:0005739 denotes mitochondrial
T238 222-232 CHEBI:35366 denotes fatty acid
T239 222-244 GO:0006635 denotes fatty acid β-oxidation
T240 235-244 MOP:0000568 denotes oxidation
T241 248-254 NCBITaxon:9606 denotes humans
R118 T246 T245 _lexicallyChainedTo cells,embryonic stem
R119 T246 T247 _lexicallyChainedTo cells,ES

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
T262 0-21 CHEBI:61907 denotes Medium-Chain Acyl-CoA
T263 0-35 GO_PR_EXT:medium_chain_acyl_CoA_dehydrogenase denotes Medium-Chain Acyl-CoA Dehydrogenase
T264 50-54 SO_EXT:0000704 denotes Gene
T265 64-68 NCBITaxon:10088 denotes Mice
T266 69-134 CHEBI:61907 denotes MCAD Gene Disruption in the Mouse Abstract Medium-chain acyl-CoA
T267 69-148 GO_PR_EXT:medium_chain_acyl_CoA_dehydrogenase denotes MCAD Gene Disruption in the Mouse Abstract Medium-chain acyl-CoA dehydrogenase
T268 150-154 GO_PR_EXT:medium_chain_acyl_CoA_dehydrogenase denotes MCAD
T269 208-221 GO:0005739 denotes mitochondrial
T270 222-227 CHEBI_UBERON_EXT:triglyceride_or_adipose_tissue denotes fatty
T271 222-232 CHEBI:35366 denotes fatty acid
T272 222-244 GO:0006635 denotes fatty acid β-oxidation
T273 235-244 MOP:0000568 denotes oxidation
T274 248-254 NCBITaxon:9606 denotes humans
T275 326-331 NCBITaxon:10088 denotes mouse
T276 342-346 GO_PR_EXT:medium_chain_acyl_CoA_dehydrogenase denotes MCAD
T277 359-363 GO_PR_EXT:medium_chain_acyl_CoA_dehydrogenase denotes MCAD
T278 363-364 SO_EXT:sequence_nullness_or_absence denotes
T279 365-366 SO_EXT:sequence_nullness_or_absence denotes
T280 371-375 SO_EXT:0000704 denotes gene
T281 389-398 UBERON:0000922 denotes embryonic
T282 389-403 _FRAGMENT denotes embryonic stem
T283 409-414 CL:0002322 denotes cells
T284 405-407 _FRAGMENT denotes ES
T285 409-414 CL_GO_EXT:cell denotes cells
T286 420-424 GO_PR_EXT:medium_chain_acyl_CoA_dehydrogenase denotes MCAD
T287 424-425 SO_EXT:sequence_nullness_or_absence denotes
T288 426-427 SO_EXT:sequence_nullness_or_absence denotes
T289 428-432 NCBITaxon:10088 denotes mice
T290 467-472 CHEBI_UBERON_EXT:triglyceride_or_adipose_tissue denotes fatty
T291 473-478 UBERON:0002107 denotes liver
T292 558-565 UBERON:0000948 denotes cardiac
T293 582-586 GO_PR_EXT:medium_chain_acyl_CoA_dehydrogenase denotes MCAD
T294 586-587 SO_EXT:sequence_nullness_or_absence denotes
T295 588-589 SO_EXT:sequence_nullness_or_absence denotes
T296 590-594 NCBITaxon:10088 denotes mice
T297 621-626 NCBITaxon:9606 denotes human
T298 627-631 GO_PR_EXT:medium_chain_acyl_CoA_dehydrogenase denotes MCAD
T299 664-672 PATO_UBERON_EXT:neonate_or_newborn denotes neonatal
T300 686-690 GO_PR_EXT:medium_chain_acyl_CoA_dehydrogenase denotes MCAD
T301 690-691 SO_EXT:sequence_nullness_or_absence denotes
T302 692-693 SO_EXT:sequence_nullness_or_absence denotes
T303 694-698 NCBITaxon_UBERON_EXT:pup denotes pups
T304 776-780 GO_PR_EXT:medium_chain_acyl_CoA_dehydrogenase denotes MCAD
T305 805-809 GO_PR_EXT:medium_chain_acyl_CoA_dehydrogenase denotes MCAD
R120 T283 T282 _lexicallyChainedTo cells,embryonic stem
R121 T283 T284 _lexicallyChainedTo cells,ES