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PMC:1584416 / 457-726 JSONTXT

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craft-sa-dev

Id Subject Object Predicate Lexical cue
T151 8-10 CC denotes or
T152 11-18 JJ denotes genetic
T153 19-29 NN denotes background
T154 29-30 . denotes .
T155 30-209 sentence denotes We addressed the potential of different recessive alleles to contribute to the enigmatic pleiotropy associated with XPD recessive disorders in compound heterozygous mouse models.
T156 31-33 PRP denotes We
T157 34-43 VBD denotes addressed
T158 44-47 DT denotes the
T159 48-57 NN denotes potential
T160 58-60 IN denotes of
T161 61-70 JJ denotes different
T162 81-88 NNS denotes alleles
T163 71-80 JJ denotes recessive
T164 89-91 TO denotes to
T165 92-102 VB denotes contribute
T166 103-105 IN denotes to
T167 106-109 DT denotes the
T168 120-130 NN denotes pleiotropy
T169 110-119 JJ denotes enigmatic
T170 131-141 VBN denotes associated
T171 142-146 IN denotes with
T172 147-150 NN denotes XPD
T173 161-170 NNS denotes disorders
T174 151-160 JJ denotes recessive
T175 171-173 IN denotes in
T176 174-182 NN denotes compound
T177 202-208 NNS denotes models
T178 183-195 JJ denotes heterozygous
T179 196-201 NN denotes mouse
T180 208-209 . denotes .
T182 210-221 NNS denotes Alterations
T184 222-224 IN denotes in
T185 225-229 DT denotes this
T186 240-248 NN denotes helicase
T187 230-239 JJ denotes essential
T188 248-250 , denotes ,
T189 250-254 IN denotes with
T190 255-264 NNS denotes functions
T191 265-267 IN denotes in
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
R86 T177 T175 pobj models,in
R87 T178 T177 amod heterozygous,models
R88 T179 T177 compound mouse,models
R93 T186 T184 pobj helicase,in
R94 T187 T186 amod essential,helicase
R63 T152 T153 amod genetic,background
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
R85 T176 T177 nmod compound,models
R89 T180 T157 punct .,addressed
R91 T184 T182 prep in,Alterations
R92 T185 T186 det this,helicase
R95 T188 T186 punct ", ",helicase
R96 T189 T186 prep with,helicase
R97 T190 T189 pobj functions,with
R98 T191 T190 prep in,functions

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
T26 11-18 SO:0000704 denotes genetic
T27 81-88 SO:0001023 denotes alleles
T28 147-150 PR:000007164 denotes XPD
T29 196-201 NCBITaxon:10088 denotes mouse

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
T56 11-18 SO_EXT:0000704 denotes genetic
T57 81-88 SO_EXT:0001023 denotes alleles
T58 147-150 PR_EXT:000007164 denotes XPD
T59 196-201 NCBITaxon:10088 denotes mouse
T60 210-221 SO_EXT:sequence_alteration_entity_or_process denotes Alterations
T61 240-248 GO_EXT:0004386 denotes helicase