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PMC:1584416 / 32357-33966 JSONTXT

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Id Subject Object Predicate Lexical cue
T6041 0-9 NN denotes Potential
T6042 10-12 IN denotes of
T6043 13-21 VBN denotes Combined
T6044 32-39 NNS denotes Alleles
T6045 22-31 JJ denotes Recessive
T6046 40-42 TO denotes to
T6047 43-49 VB denotes Affect
T6048 50-60 JJ denotes Phenotypic
T6049 61-70 NN denotes Diversity
T6050 71-73 IN denotes in
T6051 74-81 NNS denotes Mammals
T6052 81-190 sentence denotes In humans, the clinical relevance of biallelic effects such as interallelic complementation remains unknown.
T6053 82-84 IN denotes In
T6054 174-181 VBZ denotes remains
T6055 85-91 NNS denotes humans
T6056 91-93 , denotes ,
T6057 93-96 DT denotes the
T6058 106-115 NN denotes relevance
T6059 97-105 JJ denotes clinical
T6060 116-118 IN denotes of
T6061 119-128 JJ denotes biallelic
T6062 129-136 NNS denotes effects
T6063 137-141 JJ denotes such
T6064 142-144 IN denotes as
T6065 145-157 JJ denotes interallelic
T6066 158-173 NN denotes complementation
T6067 182-189 JJ denotes unknown
T6068 189-190 . denotes .
T6069 190-434 sentence denotes Although interallelic complementation between two endogenous mutant alleles has been described in cells from a compound heterozygous patient with methylmalonic acidaemia, no observable effects on disease outcome were noted in the patient [28].
T6070 191-199 IN denotes Although
T6071 276-285 VBN denotes described
T6072 200-212 JJ denotes interallelic
T6073 213-228 NN denotes complementation
T6074 229-236 IN denotes between
T6075 237-240 CD denotes two
T6076 259-266 NNS denotes alleles
T6077 241-251 JJ denotes endogenous
T6078 252-258 JJ denotes mutant
T6079 267-270 VBZ denotes has
T6080 271-275 VBN denotes been
T6081 408-413 VBN denotes noted
T6082 286-288 IN denotes in
T6083 289-294 NNS denotes cells
T6084 295-299 IN denotes from
T6085 300-301 DT denotes a
T6086 324-331 NN denotes patient
T6087 302-310 NN denotes compound
T6088 311-323 JJ denotes heterozygous
T6089 332-336 IN denotes with
T6090 337-350 JJ denotes methylmalonic
T6091 351-360 NN denotes acidaemia
T6092 360-362 , denotes ,
T6093 362-364 DT denotes no
T6094 376-383 NNS denotes effects
T6095 365-375 JJ denotes observable
T6096 384-386 IN denotes on
T6097 387-394 NN denotes disease
T6098 395-402 NN denotes outcome
T6099 403-407 VBD denotes were
T6100 414-416 IN denotes in
T6101 417-420 DT denotes the
T6102 421-428 NN denotes patient
T6103 429-430 -LRB- denotes [
T6104 430-432 CD denotes 28
T6105 432-433 -RRB- denotes ]
T6106 433-434 . denotes .
T6107 434-652 sentence denotes Thus, to the best of our knowledge, the amelioration of progeroid features observed here is the first in vivo demonstration in compound heterozygous animals of interallelic complementation relevant to a human disease.
T6108 435-439 RB denotes Thus
T6109 524-526 VBZ denotes is
T6110 439-441 , denotes ,
T6111 441-443 IN denotes to
T6112 444-447 DT denotes the
T6113 448-452 JJS denotes best
T6114 453-455 IN denotes of
T6115 456-459 PRP$ denotes our
T6116 460-469 NN denotes knowledge
T6117 469-471 , denotes ,
T6118 471-474 DT denotes the
T6119 475-487 NN denotes amelioration
T6120 488-490 IN denotes of
T6121 491-500 JJ denotes progeroid
T6122 501-509 NNS denotes features
T6123 510-518 VBN denotes observed
T6124 519-523 RB denotes here
T6125 527-530 DT denotes the
T6126 545-558 NN denotes demonstration
T6127 531-536 JJ denotes first
T6128 537-539 FW denotes in
T6129 540-544 FW denotes vivo
T6130 559-561 IN denotes in
T6131 562-570 NN denotes compound
T6132 584-591 NNS denotes animals
T6133 571-583 JJ denotes heterozygous
T6134 592-594 IN denotes of
T6135 595-607 JJ denotes interallelic
T6136 608-623 NN denotes complementation
T6137 624-632 JJ denotes relevant
T6138 633-635 IN denotes to
T6139 636-637 DT denotes a
T6140 644-651 NN denotes disease
T6141 638-643 JJ denotes human
T6142 651-652 . denotes .
T6143 652-1028 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 653-660 VBG denotes Keeping
T6145 1002-1004 VBZ denotes is
T6146 661-663 IN denotes in
T6147 664-668 NN denotes mind
T6148 669-673 IN denotes that
T6149 825-831 VB denotes result
T6150 674-677 DT denotes the
T6151 685-692 NNS denotes alleles
T6152 678-679 SYM denotes ~
T6153 679-684 CD denotes 1,200
T6154 693-698 VBN denotes known
T6155 699-701 TO denotes to
T6156 702-707 VB denotes exist
T6157 708-711 IN denotes for
T6158 712-715 DT denotes the
T6159 721-725 NN denotes gene
T6160 716-720 NN denotes CTRF
T6161 726-736 VBN denotes implicated
T6162 737-739 IN denotes in
T6163 740-743 DT denotes the
T6164 771-779 NN denotes disorder
T6165 744-750 JJ denotes common
T6166 751-760 JJ denotes autosomal
T6167 761-770 JJ denotes recessive
T6168 780-786 JJ denotes cystic
T6169 787-795 NN denotes fibrosis
T6170 796-801 RB denotes alone
T6171 802-803 -LRB- denotes [
T6172 803-805 CD denotes 29
T6173 805-806 -RRB- denotes ]
T6174 807-810 MD denotes can
T6175 811-824 RB denotes theoretically
T6176 832-834 IN denotes in
T6177 835-836 SYM denotes ~
T6178 836-843 CD denotes 700,000
T6179 862-874 NNS denotes combinations
T6180 844-853 JJ denotes different
T6181 854-861 JJ denotes allelic
T6182 874-876 , denotes ,
T6183 876-879 DT denotes the
T6184 890-896 NN denotes number
T6185 880-889 JJ denotes potential
T6186 897-899 IN denotes of
T6187 900-907 JJ denotes allelic
T6188 908-920 NNS denotes combinations
T6189 921-923 IN denotes of
T6190 924-933 JJ denotes different
T6191 944-953 NNS denotes mutations
T6192 934-943 JJ denotes recessive
T6193 954-957 CC denotes and
T6194 958-964 JJ denotes single
T6195 976-989 NNS denotes polymorphisms
T6196 965-975 NN denotes nucleotide
T6197 990-996 NN denotes genome
T6198 997-1001 JJ denotes wide
T6199 996-997 HYPH denotes -
T6200 1005-1014 RB denotes currently
T6201 1015-1027 JJ denotes incalculable
T6202 1027-1028 . denotes .
T6203 1028-1235 sentence denotes We suggest biallelic effects as a previously underestimated yet important variable in considering genotype–phenotype relationships from autosomal recessive disease to normal phenotypic diversity in mammals.
T6204 1029-1031 PRP denotes We
T6205 1032-1039 VBP denotes suggest
T6206 1040-1049 JJ denotes biallelic
T6207 1050-1057 NNS denotes effects
T6208 1058-1060 IN denotes as
T6209 1061-1062 DT denotes a
T6210 1103-1111 NN denotes variable
T6211 1063-1073 RB denotes previously
T6212 1074-1088 VBN denotes underestimated
T6213 1093-1102 JJ denotes important
T6214 1089-1092 RB denotes yet
T6215 1112-1114 IN denotes in
T6216 1115-1126 VBG denotes considering
T6217 1127-1135 NN denotes genotype
T6218 1136-1145 NN denotes phenotype
T6219 1135-1136 HYPH denotes –
T6220 1146-1159 NNS denotes relationships
T6221 1160-1164 IN denotes from
T6222 1165-1174 JJ denotes autosomal
T6223 1185-1192 NN denotes disease
T6224 1175-1184 JJ denotes recessive
T6225 1193-1195 IN denotes to
T6226 1196-1202 JJ denotes normal
T6227 1214-1223 NN denotes diversity
T6228 1203-1213 JJ denotes phenotypic
T6229 1224-1226 IN denotes in
T6230 1227-1234 NNS denotes mammals
T6231 1234-1235 . denotes .
T6232 1235-1412 sentence denotes Extension of the above concept implies that recessive mutations can enter evolutionary selection in F1 provided that the second allele carries a different recessive alteration.
T6233 1236-1245 NN denotes Extension
T6234 1267-1274 VBZ denotes implies
T6235 1246-1248 IN denotes of
T6236 1249-1252 DT denotes the
T6237 1259-1266 NN denotes concept
T6238 1253-1258 JJ denotes above
T6239 1275-1279 IN denotes that
T6240 1304-1309 VB denotes enter
T6241 1280-1289 JJ denotes recessive
T6242 1290-1299 NNS denotes mutations
T6243 1300-1303 MD denotes can
T6244 1310-1322 JJ denotes evolutionary
T6245 1323-1332 NN denotes selection
T6246 1333-1335 IN denotes in
T6247 1336-1338 NN denotes F1
T6248 1339-1347 VBN denotes provided
T6249 1348-1352 IN denotes that
T6250 1371-1378 VBZ denotes carries
T6251 1353-1356 DT denotes the
T6252 1364-1370 NN denotes allele
T6253 1357-1363 JJ denotes second
T6254 1379-1380 DT denotes a
T6255 1401-1411 NN denotes alteration
T6256 1381-1390 JJ denotes different
T6257 1391-1400 JJ denotes recessive
T6258 1411-1412 . denotes .
T6259 1412-1609 sentence denotes Finally, our data highlight the potential of clinically relevant alleles previously designated as null, with little or no detectable expression or activity, to nonetheless contribute to phenotype.
T6260 1413-1420 RB denotes Finally
T6261 1431-1440 VBP denotes highlight
T6262 1420-1422 , denotes ,
T6263 1422-1425 PRP$ denotes our
T6264 1426-1430 NNS denotes data
T6265 1441-1444 DT denotes the
T6266 1445-1454 NN denotes potential
T6267 1455-1457 IN denotes of
T6268 1458-1468 RB denotes clinically
T6269 1469-1477 JJ denotes relevant
T6270 1478-1485 NNS denotes alleles
T6271 1486-1496 RB denotes previously
T6272 1497-1507 VBN denotes designated
T6273 1508-1510 IN denotes as
T6274 1511-1515 JJ denotes null
T6275 1515-1517 , denotes ,
T6276 1517-1521 IN denotes with
T6277 1522-1528 JJ denotes little
T6278 1546-1556 NN denotes expression
T6279 1529-1531 CC denotes or
T6280 1532-1534 DT denotes no
T6281 1535-1545 JJ denotes detectable
T6282 1557-1559 CC denotes or
T6283 1560-1568 NN denotes activity
T6284 1568-1570 , denotes ,
T6285 1570-1572 TO denotes to
T6286 1585-1595 VB denotes contribute
T6287 1573-1584 RB denotes nonetheless
T6288 1596-1598 IN denotes to
T6289 1599-1608 NN denotes phenotype
T6290 1608-1609 . denotes .
R4100 T6042 T6041 prep of,Potential
R4101 T6043 T6044 amod Combined,Alleles
R4102 T6044 T6042 pobj Alleles,of
R4103 T6045 T6044 amod Recessive,Alleles
R4104 T6046 T6047 aux to,Affect
R4105 T6047 T6041 acl Affect,Potential
R4106 T6048 T6049 amod Phenotypic,Diversity
R4107 T6049 T6047 dobj Diversity,Affect
R4108 T6050 T6047 prep in,Affect
R4109 T6051 T6050 pobj Mammals,in
R4110 T6053 T6054 prep In,remains
R4111 T6055 T6053 pobj humans,In
R4112 T6056 T6054 punct ", ",remains
R4113 T6057 T6058 det the,relevance
R4114 T6058 T6054 nsubj relevance,remains
R4115 T6059 T6058 amod clinical,relevance
R4116 T6060 T6058 prep of,relevance
R4117 T6061 T6062 amod biallelic,effects
R4118 T6062 T6060 pobj effects,of
R4119 T6063 T6064 amod such,as
R4120 T6064 T6062 prep as,effects
R4121 T6065 T6066 amod interallelic,complementation
R4122 T6066 T6064 pobj complementation,as
R4123 T6067 T6054 acomp unknown,remains
R4124 T6068 T6054 punct .,remains
R4125 T6070 T6071 mark Although,described
R4126 T6071 T6081 advcl described,noted
R4127 T6072 T6073 amod interallelic,complementation
R4128 T6073 T6071 nsubjpass complementation,described
R4129 T6074 T6073 prep between,complementation
R4130 T6075 T6076 nummod two,alleles
R4131 T6076 T6074 pobj alleles,between
R4132 T6077 T6076 amod endogenous,alleles
R4133 T6078 T6076 amod mutant,alleles
R4134 T6079 T6071 aux has,described
R4135 T6080 T6071 auxpass been,described
R4136 T6082 T6071 prep in,described
R4137 T6083 T6082 pobj cells,in
R4138 T6084 T6083 prep from,cells
R4139 T6085 T6086 det a,patient
R4140 T6086 T6084 pobj patient,from
R4141 T6087 T6086 nmod compound,patient
R4142 T6088 T6086 amod heterozygous,patient
R4143 T6089 T6086 prep with,patient
R4144 T6090 T6091 amod methylmalonic,acidaemia
R4145 T6091 T6089 pobj acidaemia,with
R4146 T6092 T6081 punct ", ",noted
R4147 T6093 T6094 det no,effects
R4148 T6094 T6081 nsubjpass effects,noted
R4149 T6095 T6094 amod observable,effects
R4150 T6096 T6094 prep on,effects
R4151 T6097 T6098 compound disease,outcome
R4152 T6098 T6096 pobj outcome,on
R4153 T6099 T6081 auxpass were,noted
R4154 T6100 T6081 prep in,noted
R4155 T6101 T6102 det the,patient
R4156 T6102 T6100 pobj patient,in
R4157 T6103 T6104 punct [,28
R4158 T6104 T6081 parataxis 28,noted
R4159 T6105 T6104 punct ],28
R4160 T6106 T6081 punct .,noted
R4161 T6108 T6109 advmod Thus,is
R4162 T6110 T6109 punct ", ",is
R4163 T6111 T6109 prep to,is
R4164 T6112 T6113 det the,best
R4165 T6113 T6111 pobj best,to
R4166 T6114 T6113 prep of,best
R4167 T6115 T6116 poss our,knowledge
R4168 T6116 T6114 pobj knowledge,of
R4169 T6117 T6109 punct ", ",is
R4170 T6118 T6119 det the,amelioration
R4171 T6119 T6109 nsubj amelioration,is
R4172 T6120 T6119 prep of,amelioration
R4173 T6121 T6122 amod progeroid,features
R4174 T6122 T6120 pobj features,of
R4175 T6123 T6119 acl observed,amelioration
R4176 T6124 T6123 advmod here,observed
R4177 T6125 T6126 det the,demonstration
R4178 T6126 T6109 attr demonstration,is
R4179 T6127 T6126 amod first,demonstration
R4180 T6128 T6129 advmod in,vivo
R4181 T6129 T6126 amod vivo,demonstration
R4182 T6130 T6126 prep in,demonstration
R4183 T6131 T6132 nmod compound,animals
R4184 T6132 T6130 pobj animals,in
R4185 T6133 T6132 amod heterozygous,animals
R4186 T6134 T6132 prep of,animals
R4187 T6135 T6136 amod interallelic,complementation
R4188 T6136 T6134 pobj complementation,of
R4189 T6137 T6126 amod relevant,demonstration
R4190 T6138 T6137 prep to,relevant
R4191 T6139 T6140 det a,disease
R4192 T6140 T6138 pobj disease,to
R4193 T6141 T6140 amod human,disease
R4194 T6142 T6109 punct .,is
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
R4253 T6204 T6205 nsubj We,suggest
R4254 T6206 T6207 amod biallelic,effects
R4255 T6207 T6205 dobj effects,suggest
R4256 T6208 T6205 prep as,suggest
R4257 T6209 T6210 det a,variable
R4258 T6210 T6208 pobj variable,as
R4259 T6211 T6212 advmod previously,underestimated
R4260 T6212 T6213 amod underestimated,important
R4261 T6213 T6210 amod important,variable
R4262 T6214 T6213 advmod yet,important
R4263 T6215 T6205 prep in,suggest
R4264 T6216 T6215 pcomp considering,in
R4265 T6217 T6218 compound genotype,phenotype
R4266 T6218 T6220 compound phenotype,relationships
R4267 T6219 T6218 punct –,phenotype
R4268 T6220 T6216 dobj relationships,considering
R4269 T6221 T6216 prep from,considering
R4270 T6222 T6223 amod autosomal,disease
R4271 T6223 T6221 pobj disease,from
R4272 T6224 T6223 amod recessive,disease
R4273 T6225 T6221 prep to,from
R4274 T6226 T6227 amod normal,diversity
R4275 T6227 T6225 pobj diversity,to
R4276 T6228 T6227 amod phenotypic,diversity
R4277 T6229 T6216 prep in,considering
R4278 T6230 T6229 pobj mammals,in
R4279 T6231 T6205 punct .,suggest
R4280 T6233 T6234 nsubj Extension,implies
R4281 T6235 T6233 prep of,Extension
R4282 T6236 T6237 det the,concept
R4283 T6237 T6235 pobj concept,of
R4284 T6238 T6237 amod above,concept
R4285 T6239 T6240 mark that,enter
R4286 T6240 T6234 ccomp enter,implies
R4287 T6241 T6242 amod recessive,mutations
R4288 T6242 T6240 nsubj mutations,enter
R4289 T6243 T6240 aux can,enter
R4290 T6244 T6245 amod evolutionary,selection
R4291 T6245 T6240 dobj selection,enter
R4292 T6246 T6240 prep in,enter
R4293 T6247 T6246 pobj F1,in
R4294 T6248 T6240 prep provided,enter
R4295 T6249 T6250 mark that,carries
R4296 T6250 T6248 pcomp carries,provided
R4297 T6251 T6252 det the,allele
R4298 T6252 T6250 nsubj allele,carries
R4299 T6253 T6252 amod second,allele
R4300 T6254 T6255 det a,alteration
R4301 T6255 T6250 dobj alteration,carries
R4302 T6256 T6255 amod different,alteration
R4303 T6257 T6255 amod recessive,alteration
R4304 T6258 T6234 punct .,implies
R4305 T6260 T6261 advmod Finally,highlight
R4306 T6262 T6261 punct ", ",highlight
R4307 T6263 T6264 poss our,data
R4308 T6264 T6261 nsubj data,highlight
R4309 T6265 T6266 det the,potential
R4310 T6266 T6261 dobj potential,highlight
R4311 T6267 T6266 prep of,potential
R4312 T6268 T6269 advmod clinically,relevant
R4313 T6269 T6270 amod relevant,alleles
R4314 T6270 T6267 pobj alleles,of
R4315 T6271 T6272 advmod previously,designated
R4316 T6272 T6270 acl designated,alleles
R4317 T6273 T6272 prep as,designated
R4318 T6274 T6273 amod null,as
R4319 T6275 T6270 punct ", ",alleles
R4320 T6276 T6270 prep with,alleles
R4321 T6277 T6278 amod little,expression
R4322 T6278 T6276 pobj expression,with
R4323 T6279 T6277 cc or,little
R4324 T6280 T6277 conj no,little
R4325 T6281 T6278 amod detectable,expression
R4326 T6282 T6278 cc or,expression
R4327 T6283 T6278 conj activity,expression
R4328 T6284 T6266 punct ", ",potential
R4329 T6285 T6286 aux to,contribute
R4330 T6286 T6266 acl contribute,potential
R4331 T6287 T6286 advmod nonetheless,contribute
R4332 T6288 T6286 prep to,contribute
R4333 T6289 T6288 pobj phenotype,to
R4334 T6290 T6261 punct .,highlight

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
T5983 32-39 SO:0001023 denotes Alleles
T5984 74-81 NCBITaxon:40674 denotes Mammals
T5985 85-91 NCBITaxon:9606 denotes humans
T5986 121-128 SO:0001023 denotes allelic
T5987 150-157 SO:0001023 denotes allelic
T5988 205-212 SO:0001023 denotes allelic
T5989 259-266 SO:0001023 denotes alleles
T5990 337-350 CHEBI:30860 denotes methylmalonic
T5991 584-591 NCBITaxon:33208 denotes animals
T5992 600-607 SO:0001023 denotes allelic
T5993 638-643 NCBITaxon:9606 denotes human
T5994 685-692 SO:0001023 denotes alleles
T5995 716-720 PR:000001044 denotes CTRF
T5996 721-725 SO:0000704 denotes gene
T5997 751-760 GO:0030849 denotes autosomal
T5998 854-861 SO:0001023 denotes allelic
T5999 900-907 SO:0001023 denotes allelic
T6000 958-989 SO:0000694 denotes single nucleotide polymorphisms
T6001 990-996 SO:0001026 denotes genome
T6002 1042-1049 SO:0001023 denotes allelic
T6003 1165-1174 GO:0030849 denotes autosomal
T6004 1227-1234 NCBITaxon:40674 denotes mammals
T6005 1364-1370 SO:0001023 denotes allele
T6006 1478-1485 SO:0001023 denotes alleles
T6007 1546-1556 GO:0010467 denotes expression

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
T6008 32-39 SO_EXT:0001023 denotes Alleles
T6009 74-81 NCBITaxon:40674 denotes Mammals
T6010 85-91 NCBITaxon:9606 denotes humans
T6011 121-128 SO_EXT:0001023 denotes allelic
T6012 150-157 SO_EXT:0001023 denotes allelic
T6013 205-212 SO_EXT:0001023 denotes allelic
T6014 252-258 SO_EXT:sequence_altered_entity_or_alteration_process denotes mutant
T6015 259-266 SO_EXT:0001023 denotes alleles
T6016 289-294 CL_GO_EXT:cell denotes cells
T6017 337-350 CHEBI:30860 denotes methylmalonic
T6018 584-591 NCBITaxon:33208 denotes animals
T6019 600-607 SO_EXT:0001023 denotes allelic
T6020 638-643 NCBITaxon:9606 denotes human
T6021 685-692 SO_EXT:0001023 denotes alleles
T6022 716-720 PR_EXT:000001044 denotes CTRF
T6023 721-725 SO_EXT:0000704 denotes gene
T6024 751-760 GO:0030849 denotes autosomal
T6025 854-861 SO_EXT:0001023 denotes allelic
T6026 900-907 SO_EXT:0001023 denotes allelic
T6027 944-953 SO_EXT:sequence_alteration_entity_or_process denotes mutations
T6028 958-989 SO_EXT:0000694 denotes single nucleotide polymorphisms
T6029 965-975 CHEBI_SO_EXT:nucleotide denotes nucleotide
T6030 990-996 SO_EXT:0001026 denotes genome
T6031 1042-1049 SO_EXT:0001023 denotes allelic
T6032 1127-1135 SO_EXT:genotype_or_entity_with_genotype denotes genotype
T6033 1165-1174 GO:0030849 denotes autosomal
T6034 1227-1234 NCBITaxon:40674 denotes mammals
T6035 1290-1299 SO_EXT:sequence_alteration_entity_or_process denotes mutations
T6036 1364-1370 SO_EXT:0001023 denotes allele
T6037 1401-1411 SO_EXT:sequence_alteration_entity_or_process denotes alteration
T6038 1478-1485 SO_EXT:0001023 denotes alleles
T6039 1511-1515 SO_EXT:sequence_nullness denotes null
T6040 1546-1556 GO:0010467 denotes expression

2_test

Id Subject Object Predicate Lexical cue
17020410-9285782-84795163 430-432 9285782 denotes 28
17020410-12940920-84795164 803-805 12940920 denotes 29
T66252 430-432 9285782 denotes 28
T609 803-805 12940920 denotes 29