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PMC:1892049 / 0-201 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
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
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
R3 T871 T872 nsubj Deletion,Underlies
R4 T874 T871 prep at,Deletion
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