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PMC:314463 / 43314-43616 JSONTXT

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craft-sa-dev

Id Subject Object Predicate Lexical cue
T8863 0-302 sentence denotes In an initial description of the expression and map location of mouse Tbx15, Agulnik et al. (1998) suggested human Tbx15 that lies on Chromosome 1p11.1 as a candidate for acromegaloid facial appearance (AFA) syndrome, for which there is a weak positive LOD score to Chromosome 1p (Hughes et al. 1985).
T8864 1-3 IN denotes In
T8865 100-109 VBD denotes suggested
T8866 4-6 DT denotes an
T8867 15-26 NN denotes description
T8868 7-14 JJ denotes initial
T8869 27-29 IN denotes of
T8870 30-33 DT denotes the
T8871 34-44 NN denotes expression
T8872 45-48 CC denotes and
T8873 49-52 NN denotes map
T8874 53-61 NN denotes location
T8875 62-64 IN denotes of
T8876 65-70 NN denotes mouse
T8877 71-76 NN denotes Tbx15
T8878 76-78 , denotes ,
T8879 78-85 NNP denotes Agulnik
T8880 86-88 FW denotes et
T8881 89-92 FW denotes al.
T8882 93-94 -LRB- denotes (
T8883 94-98 CD denotes 1998
T8884 98-99 -RRB- denotes )
T8885 110-115 JJ denotes human
T8886 116-121 NN denotes Tbx15
T8887 122-126 WDT denotes that
T8888 127-131 VBZ denotes lies
T8889 132-134 IN denotes on
T8890 135-145 NN denotes Chromosome
T8891 146-152 NN denotes 1p11.1
T8892 153-155 IN denotes as
T8893 156-157 DT denotes a
T8894 158-167 NN denotes candidate
T8895 168-171 IN denotes for
T8896 172-184 JJ denotes acromegaloid
T8897 192-202 NN denotes appearance
T8898 185-191 JJ denotes facial
T8899 209-217 NN denotes syndrome
T8900 203-204 -LRB- denotes (
T8901 204-207 NN denotes AFA
T8902 207-208 -RRB- denotes )
T8903 217-219 , denotes ,
T8904 219-222 IN denotes for
T8905 235-237 VBZ denotes is
T8906 223-228 WDT denotes which
T8907 229-234 EX denotes there
T8908 238-239 DT denotes a
T8909 258-263 NN denotes score
T8910 240-244 JJ denotes weak
T8911 245-253 JJ denotes positive
T8912 254-257 NN denotes LOD
T8913 264-266 IN denotes to
T8914 267-277 NN denotes Chromosome
T8915 278-280 NN denotes 1p
T8916 281-282 -LRB- denotes (
T8917 282-288 NNP denotes Hughes
T8918 289-291 FW denotes et
T8919 292-295 FW denotes al.
T8920 296-300 CD denotes 1985
T8921 300-301 -RRB- denotes )
T8922 301-302 . denotes .
R6137 T8864 T8865 prep In,suggested
R6138 T8866 T8867 det an,description
R6139 T8867 T8864 pobj description,In
R6140 T8868 T8867 amod initial,description
R6141 T8869 T8867 prep of,description
R6142 T8870 T8871 det the,expression
R6143 T8871 T8869 pobj expression,of
R6144 T8872 T8871 cc and,expression
R6145 T8873 T8874 compound map,location
R6146 T8874 T8871 conj location,expression
R6147 T8875 T8871 prep of,expression
R6148 T8876 T8877 compound mouse,Tbx15
R6149 T8877 T8875 pobj Tbx15,of
R6150 T8878 T8865 punct ", ",suggested
R6151 T8879 T8865 nsubj Agulnik,suggested
R6152 T8880 T8881 advmod et,al.
R6153 T8881 T8879 advmod al.,Agulnik
R6154 T8882 T8879 punct (,Agulnik
R6155 T8883 T8879 npadvmod 1998,Agulnik
R6156 T8884 T8879 punct ),Agulnik
R6157 T8885 T8886 amod human,Tbx15
R6158 T8886 T8865 dobj Tbx15,suggested
R6159 T8887 T8888 dep that,lies
R6160 T8888 T8886 relcl lies,Tbx15
R6161 T8889 T8888 prep on,lies
R6162 T8890 T8891 compound Chromosome,1p11.1
R6163 T8891 T8889 pobj 1p11.1,on
R6164 T8892 T8865 prep as,suggested
R6165 T8893 T8894 det a,candidate
R6166 T8894 T8892 pobj candidate,as
R6167 T8895 T8894 prep for,candidate
R6168 T8896 T8897 amod acromegaloid,appearance
R6169 T8897 T8899 nmod appearance,syndrome
R6170 T8898 T8897 amod facial,appearance
R6171 T8899 T8895 pobj syndrome,for
R6172 T8900 T8897 punct (,appearance
R6173 T8901 T8897 appos AFA,appearance
R6174 T8902 T8899 punct ),syndrome
R6175 T8903 T8899 punct ", ",syndrome
R6176 T8904 T8905 prep for,is
R6177 T8905 T8899 relcl is,syndrome
R6178 T8906 T8904 pobj which,for
R6179 T8907 T8905 expl there,is
R6180 T8908 T8909 det a,score
R6181 T8909 T8905 attr score,is
R6182 T8910 T8909 amod weak,score
R6183 T8911 T8909 amod positive,score
R6184 T8912 T8909 compound LOD,score
R6185 T8913 T8909 prep to,score
R6186 T8914 T8915 compound Chromosome,1p
R6187 T8915 T8913 pobj 1p,to
R6188 T8916 T8917 punct (,Hughes
R6189 T8917 T8905 meta Hughes,is
R6190 T8918 T8917 nmod et,Hughes
R6191 T8919 T8917 nmod al.,Hughes
R6192 T8920 T8917 nummod 1985,Hughes
R6193 T8921 T8917 punct ),Hughes
R6194 T8922 T8865 punct .,suggested

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
T8364 34-44 GO:0010467 denotes expression
T8365 65-70 NCBITaxon:10088 denotes mouse
T8366 71-76 PR:000016145 denotes Tbx15
T8367 110-115 NCBITaxon:9606 denotes human
T8368 116-121 PR:000016145 denotes Tbx15
T8369 185-191 UBERON:0001456 denotes facial

2_test

Id Subject Object Predicate Lexical cue
14737183-9693034-84903028 94-98 9693034 denotes 1998
14737183-3989825-84903029 296-300 3989825 denotes 1985
T15261 94-98 9693034 denotes 1998
T25076 296-300 3989825 denotes 1985

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
T8463 34-44 GO:0010467 denotes expression
T8464 65-70 NCBITaxon:10088 denotes mouse
T8465 71-76 PR_EXT:000016145 denotes Tbx15
T8466 110-115 NCBITaxon:9606 denotes human
T8467 116-121 PR_EXT:000016145 denotes Tbx15
T8468 135-145 GO_SO_EXT:chromosome denotes Chromosome
T8469 185-191 UBERON:0001456 denotes facial
T8470 267-277 GO_SO_EXT:chromosome denotes Chromosome