> top > docs > PMC:1584416 > spans > 32936-33163 > annotations

PMC:1584416 / 32936-33163 JSONTXT

Annnotations TAB JSON ListView MergeView

craft-sa-dev

Id Subject Object Predicate Lexical cue
T6132 5-12 NNS denotes animals
T6134 13-15 IN denotes of
T6135 16-28 JJ denotes interallelic
T6136 29-44 NN denotes complementation
T6137 45-53 JJ denotes relevant
T6138 54-56 IN denotes to
T6139 57-58 DT denotes a
T6140 65-72 NN denotes disease
T6141 59-64 JJ denotes human
T6142 72-73 . denotes .
T6144 74-81 VBG denotes Keeping
T6146 82-84 IN denotes in
T6147 85-89 NN denotes mind
T6148 90-94 IN denotes that
T6150 95-98 DT denotes the
T6151 106-113 NNS denotes alleles
T6152 99-100 SYM denotes ~
T6153 100-105 CD denotes 1,200
T6154 114-119 VBN denotes known
T6155 120-122 TO denotes to
T6156 123-128 VB denotes exist
T6157 129-132 IN denotes for
T6158 133-136 DT denotes the
T6159 142-146 NN denotes gene
T6160 137-141 NN denotes CTRF
T6161 147-157 VBN denotes implicated
T6162 158-160 IN denotes in
T6163 161-164 DT denotes the
T6164 192-200 NN denotes disorder
T6165 165-171 JJ denotes common
T6166 172-181 JJ denotes autosomal
T6167 182-191 JJ denotes recessive
T6168 201-207 JJ denotes cystic
T6169 208-216 NN denotes fibrosis
T6170 217-222 RB denotes alone
T6171 223-224 -LRB- denotes [
T6172 224-226 CD denotes 29
T6173 226-227 -RRB- denotes ]
R4186 T6134 T6132 prep of,animals
R4187 T6135 T6136 amod interallelic,complementation
R4188 T6136 T6134 pobj complementation,of
R4190 T6138 T6137 prep to,relevant
R4191 T6139 T6140 det a,disease
R4192 T6140 T6138 pobj disease,to
R4193 T6141 T6140 amod human,disease
R4196 T6146 T6144 prep in,Keeping
R4197 T6147 T6146 pobj mind,in
R4200 T6150 T6151 det the,alleles
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

craft-ca-core-dev

Below, discontinuous spans are shown in the bag model. You can change it to the chain model.

Id Subject Object Predicate Lexical cue
T5991 5-12 NCBITaxon:33208 denotes animals
T5992 21-28 SO:0001023 denotes allelic
T5993 59-64 NCBITaxon:9606 denotes human
T5994 106-113 SO:0001023 denotes alleles
T5995 137-141 PR:000001044 denotes CTRF
T5996 142-146 SO:0000704 denotes gene
T5997 172-181 GO:0030849 denotes autosomal

craft-ca-core-ex-dev

Below, discontinuous spans are shown in the bag model. You can change it to the chain model.

Id Subject Object Predicate Lexical cue
T6018 5-12 NCBITaxon:33208 denotes animals
T6019 21-28 SO_EXT:0001023 denotes allelic
T6020 59-64 NCBITaxon:9606 denotes human
T6021 106-113 SO_EXT:0001023 denotes alleles
T6022 137-141 PR_EXT:000001044 denotes CTRF
T6023 142-146 SO_EXT:0000704 denotes gene
T6024 172-181 GO:0030849 denotes autosomal

2_test

Id Subject Object Predicate Lexical cue
17020410-12940920-84795164 224-226 12940920 denotes 29
T609 224-226 12940920 denotes 29