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PMC:1892049 / 14357-14708 JSONTXT

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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
T6241 12-22 UBERON:0002037 denotes cerebellar
T6242 53-58 PR_EXT:000015827 denotes SUMF1
T6243 59-64 PR_EXT:000009158 denotes ITPR1
T6244 65-73 SO_EXT:sequence_deletion_entity_or_process denotes deletion
T6245 84-92 SO_EXT:sequence_deletion_entity_or_process denotes deletion
T6246 203-211 SO_EXT:sequence_deletion_entity_or_process denotes deletion
T6247 226-233 SO_EXT:0000704 denotes genetic

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
T5944 12-22 UBERON:0002037 denotes cerebellar
T5945 53-58 PR:000015827 denotes SUMF1
T5946 59-64 PR:000009158 denotes ITPR1
T5947 226-233 SO:0000704 denotes genetic

craft-sa-dev

Id Subject Object Predicate Lexical cue
T7859 0-351 sentence denotes With three cerebellar ataxia families segregating a SUMF1–ITPR1 deletion, and this deletion not observed in a control population, we may reasonably conclude that the association is causal, and that the deletion is indeed the genetic basis of the disease, with SCA15 the diagnosis in the two British families as well as the original Australian family.
T7860 1-5 IN denotes With
T7861 149-157 VB denotes conclude
T7862 6-11 CD denotes three
T7863 30-38 NNS denotes families
T7864 12-22 JJ denotes cerebellar
T7865 23-29 NN denotes ataxia
T7866 39-50 VBG denotes segregating
T7867 51-52 DT denotes a
T7868 65-73 NN denotes deletion
T7869 53-58 NN denotes SUMF1
T7870 59-64 NN denotes ITPR1
T7871 58-59 HYPH denotes –
T7872 73-75 , denotes ,
T7873 75-78 CC denotes and
T7874 79-83 DT denotes this
T7875 84-92 NN denotes deletion
T7876 93-96 RB denotes not
T7877 97-105 VBN denotes observed
T7878 106-108 IN denotes in
T7879 109-110 DT denotes a
T7880 119-129 NN denotes population
T7881 111-118 NN denotes control
T7882 129-131 , denotes ,
T7883 131-133 PRP denotes we
T7884 134-137 MD denotes may
T7885 138-148 RB denotes reasonably
T7886 158-162 IN denotes that
T7887 179-181 VBZ denotes is
T7888 163-166 DT denotes the
T7889 167-178 NN denotes association
T7890 182-188 JJ denotes causal
T7891 188-190 , denotes ,
T7892 190-193 CC denotes and
T7893 194-198 IN denotes that
T7894 212-214 VBZ denotes is
T7895 199-202 DT denotes the
T7896 203-211 NN denotes deletion
T7897 215-221 RB denotes indeed
T7898 222-225 DT denotes the
T7899 234-239 NN denotes basis
T7900 226-233 JJ denotes genetic
T7901 240-242 IN denotes of
T7902 243-246 DT denotes the
T7903 247-254 NN denotes disease
T7904 254-256 , denotes ,
T7905 256-260 IN denotes with
T7906 271-280 NN denotes diagnosis
T7907 261-266 NN denotes SCA15
T7908 267-270 DT denotes the
T7909 281-283 IN denotes in
T7910 284-287 DT denotes the
T7911 300-308 NNS denotes families
T7912 288-291 CD denotes two
T7913 292-299 JJ denotes British
T7914 309-311 RB denotes as
T7915 317-319 IN denotes as
T7916 312-316 RB denotes well
T7917 320-323 DT denotes the
T7918 344-350 NN denotes family
T7919 324-332 JJ denotes original
T7920 333-343 JJ denotes Australian
T7921 350-351 . denotes .
R1820 T7860 T7861 prep With,conclude
R1822 T7862 T7863 nummod three,families
R1823 T7863 T7860 pobj families,With
R1824 T7864 T7863 amod cerebellar,families
R1825 T7865 T7863 compound ataxia,families
R1826 T7866 T7863 acl segregating,families
R1828 T7867 T7868 det a,deletion
R1829 T7868 T7866 dobj deletion,segregating
R1830 T7869 T7870 compound SUMF1,ITPR1
R1832 T7870 T7868 compound ITPR1,deletion
R1834 T7871 T7870 punct –,ITPR1
R1835 T7872 T7863 punct ", ",families
R1836 T7873 T7863 cc and,families
R1839 T7874 T7875 det this,deletion
R1841 T7875 T7863 conj deletion,families
R1842 T7876 T7877 neg not,observed
R1844 T7877 T7875 acl observed,deletion
R1845 T7878 T7877 prep in,observed
R1847 T7879 T7880 det a,population
R1848 T7880 T7878 pobj population,in
R1849 T7881 T7880 compound control,population
R1851 T7882 T7861 punct ", ",conclude
R1852 T7883 T7861 nsubj we,conclude
R1853 T7884 T7861 aux may,conclude
R1854 T7885 T7861 advmod reasonably,conclude
R1855 T7886 T7887 mark that,is
R1856 T7887 T7861 advcl is,conclude
R1858 T7888 T7889 det the,association
R1859 T7889 T7887 nsubj association,is
R1860 T7890 T7887 acomp causal,is
R1862 T7891 T7887 punct ", ",is
R1863 T7892 T7887 cc and,is
R1864 T7893 T7894 mark that,is
R1866 T7894 T7887 conj is,is
R1867 T7895 T7896 det the,deletion
R1868 T7896 T7894 nsubj deletion,is
R1870 T7897 T7894 advmod indeed,is
R1871 T7898 T7899 det the,basis
R1873 T7899 T7894 attr basis,is
R1874 T7900 T7899 amod genetic,basis
R1875 T7901 T7899 prep of,basis
R1877 T7902 T7903 det the,disease
R1878 T7903 T7901 pobj disease,of
R1879 T7904 T7894 punct ", ",is
R1881 T7905 T7906 mark with,diagnosis
R1882 T7906 T7894 advcl diagnosis,is
R1884 T7907 T7906 nsubj SCA15,diagnosis
R1885 T7908 T7906 det the,diagnosis
R1886 T7909 T7906 prep in,diagnosis
R1888 T7910 T7911 det the,families
R1889 T7911 T7909 pobj families,in
R1890 T7912 T7911 nummod two,families
R1892 T7913 T7911 amod British,families
R1893 T7914 T7915 advmod as,as
R1894 T7915 T7911 cc as,families
R1896 T7916 T7915 advmod well,as
R1897 T7917 T7918 det the,family
R1898 T7918 T7911 conj family,families
R1899 T7919 T7918 amod original,family
R1901 T7920 T7918 amod Australian,family
R1902 T7921 T7861 punct .,conclude