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PMC:1892049 / 28-234 JSONTXT 5 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue
T876 0-6 NN denotes Ataxia
T877 7-9 IN denotes in
T878 10-14 NNS denotes Mice
T879 15-18 CC denotes and
T880 19-34 JJ denotes Spinocerebellar
T881 35-41 NN denotes Ataxia
T882 42-44 CD denotes 15
T883 45-47 IN denotes in
T884 48-54 NNS denotes Humans
T887 54-188 sentence denotes ITPR1 Deletion Causes Ataxia Abstract We observed a severe autosomal recessive movement disorder in mice used within our laboratory.
T888 94-96 PRP denotes We
T889 97-105 VBD denotes observed
T890 106-107 DT denotes a
T892 108-114 JJ denotes severe
T893 115-124 JJ denotes autosomal
T894 125-134 JJ denotes recessive
T895 135-143 NN denotes movement
T891 144-152 NN denotes disorder
T896 153-155 IN denotes in
T897 156-160 NNS denotes mice
T898 161-165 VBN denotes used
T899 166-172 IN denotes within
T900 173-176 PRP$ denotes our
T901 177-187 NN denotes laboratory
T902 187-188 . denotes .
T904 189-191 PRP denotes We
T905 192-199 VBD denotes pursued
T906 200-201 DT denotes a
R10 T880 T881 amod Spinocerebellar,Ataxia
R11 T881 T876 conj Ataxia,Ataxia
R12 T882 T881 nummod 15,Ataxia
R13 T883 T881 prep in,Ataxia
R14 T884 T883 pobj Humans,in
R15 T888 T889 nsubj We,observed
R16 T890 T891 det a,disorder
R17 T891 T889 dobj disorder,observed
R18 T892 T891 amod severe,disorder
R19 T893 T891 amod autosomal,disorder
R20 T894 T891 amod recessive,disorder
R21 T895 T891 compound movement,disorder
R22 T896 T889 prep in,observed
R23 T897 T896 pobj mice,in
R24 T898 T897 acl used,mice
R25 T899 T898 prep within,used
R26 T900 T901 poss our,laboratory
R27 T901 T899 pobj laboratory,within
R28 T902 T889 punct .,observed
R29 T904 T905 nsubj We,pursued
R7 T877 T876 prep in,Ataxia
R8 T878 T877 pobj Mice,in
R9 T879 T876 cc and,Ataxia