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PMC:1892049 / 0-351 JSONTXT 5 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue
T871 0-8 NN denotes Deletion
T873 0-82 sentence denotes Deletion at ITPR1 Underlies Ataxia in Mice and Spinocerebellar Ataxia 15 in Humans
T874 9-11 IN denotes at
T875 12-17 NNP denotes ITPR1
T872 18-27 VBZ denotes Underlies
T876 28-34 NN denotes Ataxia
T877 35-37 IN denotes in
T878 38-42 NNS denotes Mice
T879 43-46 CC denotes and
T880 47-62 JJ denotes Spinocerebellar
T881 63-69 NN denotes Ataxia
T882 70-72 CD denotes 15
T883 73-75 IN denotes in
T884 76-82 NNS denotes Humans
T887 82-216 sentence denotes ITPR1 Deletion Causes Ataxia Abstract We observed a severe autosomal recessive movement disorder in mice used within our laboratory.
T888 122-124 PRP denotes We
T889 125-133 VBD denotes observed
T890 134-135 DT denotes a
T892 136-142 JJ denotes severe
T893 143-152 JJ denotes autosomal
T894 153-162 JJ denotes recessive
T895 163-171 NN denotes movement
T891 172-180 NN denotes disorder
T896 181-183 IN denotes in
T897 184-188 NNS denotes mice
T898 189-193 VBN denotes used
T899 194-200 IN denotes within
T900 201-204 PRP$ denotes our
T901 205-215 NN denotes laboratory
T902 215-216 . denotes .
T904 217-219 PRP denotes We
T905 220-227 VBD denotes pursued
T906 228-229 DT denotes a
T907 230-236 NN denotes series
T908 237-239 IN denotes of
T909 240-251 NNS denotes experiments
T910 252-254 TO denotes to
T911 255-261 VB denotes define
T912 262-265 DT denotes the
T914 266-273 JJ denotes genetic
T913 274-280 NN denotes lesion
T915 281-291 VBG denotes underlying
T916 292-296 DT denotes this
T917 297-305 NN denotes disorder
T918 306-309 CC denotes and
T919 310-312 TO denotes to
T920 313-321 VB denotes identify
T921 322-323 DT denotes a
T923 324-331 JJ denotes cognate
T922 332-339 NN denotes disease
T924 340-342 IN denotes in
T925 343-349 NNS denotes humans
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
R3 T871 T872 nsubj Deletion,Underlies
R30 T906 T907 det a,series
R31 T907 T905 dobj series,pursued
R32 T908 T907 prep of,series
R33 T909 T908 pobj experiments,of
R34 T910 T911 aux to,define
R35 T911 T905 advcl define,pursued
R36 T912 T913 det the,lesion
R37 T913 T911 dobj lesion,define
R38 T914 T913 amod genetic,lesion
R39 T915 T913 acl underlying,lesion
R4 T874 T871 prep at,Deletion
R40 T916 T917 det this,disorder
R41 T917 T915 dobj disorder,underlying
R42 T918 T911 cc and,define
R43 T919 T920 aux to,identify
R44 T920 T911 conj identify,define
R45 T921 T922 det a,disease
R46 T922 T920 dobj disease,identify
R47 T923 T922 amod cognate,disease
R48 T924 T920 prep in,identify
R49 T925 T924 pobj humans,in
R5 T875 T874 pobj ITPR1,at
R6 T876 T872 dobj Ataxia,Underlies
R7 T877 T876 prep in,Ataxia
R8 T878 T877 pobj Mice,in
R9 T879 T876 cc and,Ataxia