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PMC:1584416 / 33009-33385 JSONTXT

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craft-sa-dev

Id Subject Object Predicate Lexical cue
T6143 0-376 sentence denotes Keeping in mind that the ~1,200 alleles known to exist for the CTRF gene implicated in the common autosomal recessive disorder cystic fibrosis alone [29] can theoretically result in ~700,000 different allelic combinations, the potential number of allelic combinations of different recessive mutations and single nucleotide polymorphisms genome-wide is currently incalculable.
T6144 1-8 VBG denotes Keeping
T6145 350-352 VBZ denotes is
T6146 9-11 IN denotes in
T6147 12-16 NN denotes mind
T6148 17-21 IN denotes that
T6149 173-179 VB denotes result
T6150 22-25 DT denotes the
T6151 33-40 NNS denotes alleles
T6152 26-27 SYM denotes ~
T6153 27-32 CD denotes 1,200
T6154 41-46 VBN denotes known
T6155 47-49 TO denotes to
T6156 50-55 VB denotes exist
T6157 56-59 IN denotes for
T6158 60-63 DT denotes the
T6159 69-73 NN denotes gene
T6160 64-68 NN denotes CTRF
T6161 74-84 VBN denotes implicated
T6162 85-87 IN denotes in
T6163 88-91 DT denotes the
T6164 119-127 NN denotes disorder
T6165 92-98 JJ denotes common
T6166 99-108 JJ denotes autosomal
T6167 109-118 JJ denotes recessive
T6168 128-134 JJ denotes cystic
T6169 135-143 NN denotes fibrosis
T6170 144-149 RB denotes alone
T6171 150-151 -LRB- denotes [
T6172 151-153 CD denotes 29
T6173 153-154 -RRB- denotes ]
T6174 155-158 MD denotes can
T6175 159-172 RB denotes theoretically
T6176 180-182 IN denotes in
T6177 183-184 SYM denotes ~
T6178 184-191 CD denotes 700,000
T6179 210-222 NNS denotes combinations
T6180 192-201 JJ denotes different
T6181 202-209 JJ denotes allelic
T6182 222-224 , denotes ,
T6183 224-227 DT denotes the
T6184 238-244 NN denotes number
T6185 228-237 JJ denotes potential
T6186 245-247 IN denotes of
T6187 248-255 JJ denotes allelic
T6188 256-268 NNS denotes combinations
T6189 269-271 IN denotes of
T6190 272-281 JJ denotes different
T6191 292-301 NNS denotes mutations
T6192 282-291 JJ denotes recessive
T6193 302-305 CC denotes and
T6194 306-312 JJ denotes single
T6195 324-337 NNS denotes polymorphisms
T6196 313-323 NN denotes nucleotide
T6197 338-344 NN denotes genome
T6198 345-349 JJ denotes wide
T6199 344-345 HYPH denotes -
T6200 353-362 RB denotes currently
T6201 363-375 JJ denotes incalculable
T6202 375-376 . denotes .
R4195 T6144 T6145 advcl Keeping,is
R4196 T6146 T6144 prep in,Keeping
R4197 T6147 T6146 pobj mind,in
R4198 T6148 T6149 mark that,result
R4199 T6149 T6144 ccomp result,Keeping
R4200 T6150 T6151 det the,alleles
R4201 T6151 T6149 nsubj alleles,result
R4202 T6152 T6153 punct ~,"1,200"
R4203 T6153 T6151 nummod "1,200",alleles
R4204 T6154 T6151 acl known,alleles
R4205 T6155 T6156 aux to,exist
R4206 T6156 T6154 xcomp exist,known
R4207 T6157 T6156 prep for,exist
R4208 T6158 T6159 det the,gene
R4209 T6159 T6157 pobj gene,for
R4210 T6160 T6159 compound CTRF,gene
R4211 T6161 T6159 acl implicated,gene
R4212 T6162 T6161 prep in,implicated
R4213 T6163 T6164 det the,disorder
R4214 T6164 T6162 pobj disorder,in
R4215 T6165 T6164 amod common,disorder
R4216 T6166 T6164 amod autosomal,disorder
R4217 T6167 T6164 amod recessive,disorder
R4218 T6168 T6169 amod cystic,fibrosis
R4219 T6169 T6164 appos fibrosis,disorder
R4220 T6170 T6161 advmod alone,implicated
R4221 T6171 T6172 punct [,29
R4222 T6172 T6154 parataxis 29,known
R4223 T6173 T6172 punct ],29
R4224 T6174 T6149 aux can,result
R4225 T6175 T6149 advmod theoretically,result
R4226 T6176 T6149 prep in,result
R4227 T6177 T6178 punct ~,"700,000"
R4228 T6178 T6179 nummod "700,000",combinations
R4229 T6179 T6176 pobj combinations,in
R4230 T6180 T6179 amod different,combinations
R4231 T6181 T6179 amod allelic,combinations
R4232 T6182 T6145 punct ", ",is
R4233 T6183 T6184 det the,number
R4234 T6184 T6145 nsubj number,is
R4235 T6185 T6184 amod potential,number
R4236 T6186 T6184 prep of,number
R4237 T6187 T6188 amod allelic,combinations
R4238 T6188 T6186 pobj combinations,of
R4239 T6189 T6188 prep of,combinations
R4240 T6190 T6191 amod different,mutations
R4241 T6191 T6189 pobj mutations,of
R4242 T6192 T6191 amod recessive,mutations
R4243 T6193 T6191 cc and,mutations
R4244 T6194 T6195 amod single,polymorphisms
R4245 T6195 T6191 conj polymorphisms,mutations
R4246 T6196 T6195 compound nucleotide,polymorphisms
R4247 T6197 T6198 npadvmod genome,wide
R4248 T6198 T6184 amod wide,number
R4249 T6199 T6198 punct -,wide
R4250 T6200 T6145 advmod currently,is
R4251 T6201 T6145 acomp incalculable,is
R4252 T6202 T6145 punct .,is

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
T5994 33-40 SO:0001023 denotes alleles
T5995 64-68 PR:000001044 denotes CTRF
T5996 69-73 SO:0000704 denotes gene
T5997 99-108 GO:0030849 denotes autosomal
T5998 202-209 SO:0001023 denotes allelic
T5999 248-255 SO:0001023 denotes allelic
T6000 306-337 SO:0000694 denotes single nucleotide polymorphisms
T6001 338-344 SO:0001026 denotes genome

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
T6021 33-40 SO_EXT:0001023 denotes alleles
T6022 64-68 PR_EXT:000001044 denotes CTRF
T6023 69-73 SO_EXT:0000704 denotes gene
T6024 99-108 GO:0030849 denotes autosomal
T6025 202-209 SO_EXT:0001023 denotes allelic
T6026 248-255 SO_EXT:0001023 denotes allelic
T6027 292-301 SO_EXT:sequence_alteration_entity_or_process denotes mutations
T6028 306-337 SO_EXT:0000694 denotes single nucleotide polymorphisms
T6029 313-323 CHEBI_SO_EXT:nucleotide denotes nucleotide
T6030 338-344 SO_EXT:0001026 denotes genome

2_test

Id Subject Object Predicate Lexical cue
17020410-12940920-84795164 151-153 12940920 denotes 29
T609 151-153 12940920 denotes 29