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PMC:1166548 / 0-382 JSONTXT

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craft-sa-dev

Id Subject Object Predicate Lexical cue
T139 0-9 JJ denotes Potential
T140 18-27 NNS denotes modifiers
T141 0-118 sentence denotes Potential genetic modifiers of the cystic fibrosis intestinal inflammatory phenotype on mouse chromosomes 1, 9, and 10
T142 10-17 JJ denotes genetic
T143 28-30 IN denotes of
T144 31-34 DT denotes the
T145 75-84 NN denotes phenotype
T146 35-41 JJ denotes cystic
T147 42-50 NN denotes fibrosis
T148 51-61 JJ denotes intestinal
T149 62-74 JJ denotes inflammatory
T150 85-87 IN denotes on
T151 88-93 NN denotes mouse
T152 106-107 CD denotes 1
T153 94-105 NNS denotes chromosomes
T155 109-110 CD denotes 9
T156 110-112 , denotes ,
T157 112-115 CC denotes and
T158 116-118 CD denotes 10
T159 118-119 sentence denotes
T160 129-139 sentence denotes Background
T161 129-139 NN denotes Background
T162 139-346 sentence denotes Although cystic fibrosis is caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene, the severity of disease is highly variable indicating the influence of modifier genes.
T163 140-148 IN denotes Although
T164 168-174 VBN denotes caused
T165 149-155 JJ denotes cystic
T166 156-164 NN denotes fibrosis
T167 165-167 VBZ denotes is
T168 284-286 VBZ denotes is
T169 175-177 IN denotes by
T170 178-187 NNS denotes mutations
T171 188-190 IN denotes in
T172 191-194 DT denotes the
T173 254-258 NN denotes gene
T174 195-201 JJ denotes cystic
T175 237-246 NN denotes regulator
T176 202-210 NN denotes fibrosis
T177 211-224 JJ denotes transmembrane
T178 225-236 NN denotes conductance
T179 247-248 -LRB- denotes (
T180 248-252 NN denotes CFTR
T181 252-253 -RRB- denotes )
T182 258-260 , denotes ,
T183 260-263 DT denotes the
T184 264-272 NN denotes severity
T185 273-275 IN denotes of
T186 276-283 NN denotes disease
T187 287-293 RB denotes highly
T188 294-302 JJ denotes variable
T189 303-313 VBG denotes indicating
T190 314-317 DT denotes the
T191 318-327 NN denotes influence
T192 328-330 IN denotes of
T193 331-339 NN denotes modifier
T194 340-345 NNS denotes genes
T195 345-346 . denotes .
T197 347-350 DT denotes The
T198 351-361 NNS denotes intestines
T200 362-364 IN denotes of
T201 365-369 NN denotes Cftr
T202 370-379 JJ denotes deficient
T154 107-109 , denotes ,
R5 T145 T143 pobj phenotype,of
R6 T146 T147 amod cystic,fibrosis
R7 T147 T145 nmod fibrosis,phenotype
R8 T148 T145 amod intestinal,phenotype
R9 T149 T145 amod inflammatory,phenotype
R12 T152 T150 pobj 1,on
R13 T153 T152 nmod chromosomes,1
R14 T155 T152 conj 9,1
R15 T156 T155 punct ", ",9
R16 T157 T155 cc and,9
R17 T158 T155 conj 10,9
R18 T163 T164 mark Although,caused
R19 T164 T168 advcl caused,is
R23 T169 T164 agent by,caused
R24 T170 T169 pobj mutations,by
R25 T171 T170 prep in,mutations
R26 T172 T173 det the,gene
R27 T173 T171 pobj gene,in
R29 T175 T173 nmod regulator,gene
R30 T176 T175 nmod fibrosis,regulator
R31 T177 T175 amod transmembrane,regulator
R32 T178 T175 nmod conductance,regulator
R36 T182 T168 punct ", ",is
R37 T183 T184 det the,severity
R38 T184 T168 nsubj severity,is
R39 T185 T184 prep of,severity
R40 T186 T185 pobj disease,of
R41 T187 T188 advmod highly,variable
R42 T188 T168 acomp variable,is
R43 T189 T168 advcl indicating,is
R44 T190 T191 det the,influence
R45 T191 T189 dobj influence,indicating
R46 T192 T191 prep of,influence
R47 T193 T194 compound modifier,genes
R48 T194 T192 pobj genes,of
R49 T195 T168 punct .,is
R50 T197 T198 det The,intestines
R52 T200 T198 prep of,intestines
R53 T201 T202 npadvmod Cftr,deficient
R371 T154 T152 punct ", ",1
R1 T139 T140 amod Potential,modifiers
R2 T142 T140 amod genetic,modifiers
R3 T143 T140 prep of,modifiers
R4 T144 T145 det the,phenotype
R10 T150 T140 prep on,modifiers
R11 T151 T152 nmod mouse,1
R20 T165 T166 amod cystic,fibrosis
R21 T166 T164 nsubjpass fibrosis,caused
R22 T167 T164 auxpass is,caused
R28 T174 T175 amod cystic,regulator
R33 T179 T175 punct (,regulator
R34 T180 T175 appos CFTR,regulator
R35 T181 T173 punct ),gene

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
T74 10-17 SO_EXT:0000704 denotes genetic
T75 51-61 UBERON:0000160 denotes intestinal
T76 62-74 GO_PATO_EXT:inflammatory_process_or_quality denotes inflammatory
T77 88-93 NCBITaxon:10088 denotes mouse
T78 94-105 GO_SO_EXT:chromosome denotes chromosomes
T79 178-187 SO_EXT:sequence_alteration_entity_or_process denotes mutations
T80 195-246 PR_EXT:000001044 denotes cystic fibrosis transmembrane conductance regulator
T81 211-236 GO:0055085 denotes transmembrane conductance
T82 216-224 GO:0016020 denotes membrane
T83 237-246 GO_EXT:regulator denotes regulator
T84 248-252 PR_EXT:000001044 denotes CFTR
T85 254-258 SO_EXT:0000704 denotes gene
T86 340-345 SO_EXT:0000704 denotes genes
T87 351-361 UBERON:0000160 denotes intestines
T88 365-369 PR_EXT:000001044 denotes Cftr

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
T37 254-258 SO:0000704 denotes gene
T38 340-345 SO:0000704 denotes genes
T39 351-361 UBERON:0000160 denotes intestines
T40 365-369 PR:000001044 denotes Cftr
T30 10-17 SO:0000704 denotes genetic
T31 51-61 UBERON:0000160 denotes intestinal
T32 88-93 NCBITaxon:10088 denotes mouse
T33 195-246 PR:000001044 denotes cystic fibrosis transmembrane conductance regulator
T34 211-236 GO:0055085 denotes transmembrane conductance
T35 216-224 GO:0016020 denotes membrane
T36 248-252 PR:000001044 denotes CFTR