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PMC:1584416 / 208-636 JSONTXT

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craft-sa-dev

Id Subject Object Predicate Lexical cue
T97 17-19 VBZ denotes is
T110 2-5 DT denotes the
T111 11-15 NN denotes gene
T112 6-10 JJ denotes same
T113 15-17 , denotes ,
T114 113-123 VBN denotes documented
T115 20-26 JJ denotes common
T116 27-29 IN denotes in
T117 30-35 JJ denotes human
T118 46-53 NN denotes disease
T119 36-45 JJ denotes recessive
T120 53-55 , denotes ,
T121 55-58 PRP$ denotes its
T122 59-68 NN denotes potential
T123 69-71 TO denotes to
T124 72-78 VB denotes impact
T125 79-86 NN denotes disease
T126 87-94 NN denotes outcome
T127 95-98 VBZ denotes has
T128 99-102 RB denotes not
T129 103-107 VBN denotes been
T130 108-112 RB denotes well
T131 123-124 . denotes .
T132 124-279 sentence denotes This is most likely because of the inherent difficulty in distinguishing specific biallelic effects from differences in environment or genetic background.
T133 125-129 DT denotes This
T134 130-132 VBZ denotes is
T135 133-137 RBS denotes most
T136 138-144 RB denotes likely
T137 145-152 IN denotes because
T138 153-155 IN denotes of
T139 156-159 DT denotes the
T140 169-179 NN denotes difficulty
T141 160-168 JJ denotes inherent
T142 180-182 IN denotes in
T143 183-197 VBG denotes distinguishing
T144 198-206 JJ denotes specific
T145 217-224 NNS denotes effects
T146 207-216 JJ denotes biallelic
T147 225-229 IN denotes from
T148 230-241 NNS denotes differences
T149 242-244 IN denotes in
T150 245-256 NN denotes environment
T151 257-259 CC denotes or
T152 260-267 JJ denotes genetic
T153 268-278 NN denotes background
T154 278-279 . denotes .
T156 280-282 PRP denotes We
T157 283-292 VBD denotes addressed
T158 293-296 DT denotes the
T159 297-306 NN denotes potential
T160 307-309 IN denotes of
T161 310-319 JJ denotes different
T162 330-337 NNS denotes alleles
T163 320-329 JJ denotes recessive
T164 338-340 TO denotes to
T165 341-351 VB denotes contribute
T166 352-354 IN denotes to
T167 355-358 DT denotes the
T168 369-379 NN denotes pleiotropy
T169 359-368 JJ denotes enigmatic
T170 380-390 VBN denotes associated
T171 391-395 IN denotes with
T172 396-399 NN denotes XPD
T173 410-419 NNS denotes disorders
T174 400-409 JJ denotes recessive
T175 420-422 IN denotes in
R11 T97 T114 advcl is,documented
R24 T110 T111 det the,gene
R26 T112 T111 amod same,gene
R27 T113 T97 punct ", ",is
R31 T118 T116 pobj disease,in
R32 T119 T118 amod recessive,disease
R51 T140 T137 pobj difficulty,because
R52 T141 T140 amod inherent,difficulty
R56 T145 T143 dobj effects,distinguishing
R57 T146 T145 amod biallelic,effects
R71 T162 T160 pobj alleles,of
R72 T163 T162 amod recessive,alleles
R77 T168 T166 pobj pleiotropy,to
R78 T169 T168 amod enigmatic,pleiotropy
R82 T173 T171 pobj disorders,with
R83 T174 T173 amod recessive,disorders
R34 T121 T122 poss its,potential
R28 T115 T97 acomp common,is
R29 T116 T97 prep in,is
R30 T117 T118 amod human,disease
R33 T120 T114 punct ", ",documented
R35 T122 T114 nsubjpass potential,documented
R36 T123 T124 aux to,impact
R37 T124 T122 acl impact,potential
R38 T125 T126 compound disease,outcome
R39 T126 T124 dobj outcome,impact
R40 T127 T114 aux has,documented
R41 T128 T114 neg not,documented
R42 T129 T114 auxpass been,documented
R43 T130 T114 advmod well,documented
R44 T131 T114 punct .,documented
R45 T133 T134 nsubj This,is
R46 T135 T136 advmod most,likely
R47 T136 T137 advmod likely,because
R48 T137 T134 prep because,is
R49 T138 T137 pcomp of,because
R50 T139 T140 det the,difficulty
R53 T142 T140 prep in,difficulty
R54 T143 T142 pcomp distinguishing,in
R55 T144 T145 amod specific,effects
R58 T147 T143 prep from,distinguishing
R59 T148 T147 pobj differences,from
R60 T149 T148 prep in,differences
R61 T150 T149 pobj environment,in
R62 T151 T150 cc or,environment
R63 T152 T153 amod genetic,background
R64 T153 T150 conj background,environment
R65 T154 T134 punct .,is
R66 T156 T157 nsubj We,addressed
R67 T158 T159 det the,potential
R68 T159 T157 dobj potential,addressed
R69 T160 T159 prep of,potential
R70 T161 T162 amod different,alleles
R73 T164 T165 aux to,contribute
R74 T165 T159 acl contribute,potential
R75 T166 T165 prep to,contribute
R76 T167 T168 det the,pleiotropy
R79 T170 T168 acl associated,pleiotropy
R80 T171 T170 prep with,associated
R81 T172 T173 nmod XPD,disorders
R84 T175 T170 prep in,associated

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
T23 11-15 SO:0000704 denotes gene
T24 30-35 NCBITaxon:9606 denotes human
T25 209-216 SO:0001023 denotes allelic
T26 260-267 SO:0000704 denotes genetic
T27 330-337 SO:0001023 denotes alleles
T28 396-399 PR:000007164 denotes XPD

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
T53 11-15 SO_EXT:0000704 denotes gene
T54 30-35 NCBITaxon:9606 denotes human
T55 209-216 SO_EXT:0001023 denotes allelic
T56 260-267 SO_EXT:0000704 denotes genetic
T57 330-337 SO_EXT:0001023 denotes alleles
T58 396-399 PR_EXT:000007164 denotes XPD