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PMC:1892049 / 327-622 JSONTXT 5 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue
T922 5-12 NN denotes disease
T924 13-15 IN denotes in
T925 16-22 NNS denotes humans
T926 23-27 IN denotes with
T927 28-36 NN denotes mutation
T928 37-39 IN denotes at
T929 40-43 DT denotes the
T931 44-48 JJ denotes same
T930 49-54 NN denotes locus
T932 54-55 . denotes .
T933 55-249 sentence denotes Through linkage and sequence analysis we show here that this disorder is caused by a homozygous in-frame 18-bp deletion in Itpr1 (Itpr1Δ18/Δ18), encoding inositol 1,4,5-triphosphate receptor 1.
T934 56-63 IN denotes Through
T936 64-71 NN denotes linkage
T938 72-75 CC denotes and
T939 76-84 NN denotes sequence
T937 85-93 NN denotes analysis
T940 94-96 PRP denotes we
T935 97-101 VBP denotes show
T941 102-106 RB denotes here
T942 107-111 IN denotes that
T944 112-116 DT denotes this
T945 117-125 NN denotes disorder
T946 126-128 VBZ denotes is
T943 129-135 VBN denotes caused
T947 136-138 IN denotes by
T948 139-140 DT denotes a
T950 141-151 JJ denotes homozygous
T951 152-154 IN denotes in
T952 154-155 HYPH denotes -
T953 155-160 NN denotes frame
T954 161-163 CD denotes 18
T956 163-164 HYPH denotes -
T955 164-166 NN denotes bp
T949 167-175 NN denotes deletion
T957 176-178 IN denotes in
T958 179-184 NN denotes Itpr1
T959 185-186 -LRB- denotes (
T961 186-191 NN denotes Itpr1
T962 191-194 NN denotes Δ18
T963 194-195 HYPH denotes /
T960 195-198 NN denotes Δ18
T964 198-199 -RRB- denotes )
T965 199-201 , denotes ,
T966 201-209 VBG denotes encoding
T967 210-218 NN denotes inositol
T969 219-220 CD denotes 1
T971 220-221 , denotes ,
T972 221-222 CD denotes 4
T973 222-223 , denotes ,
T970 223-224 CD denotes 5
T975 224-225 HYPH denotes -
T974 225-237 NN denotes triphosphate
T968 238-246 NN denotes receptor
T976 247-248 CD denotes 1
T977 248-249 . denotes .
T979 250-251 DT denotes A
T981 252-262 RB denotes previously
T982 263-271 VBN denotes reported
T983 272-283 JJ denotes spontaneous
T984 284-289 NN denotes Itpr1
R102 T981 T982 advmod previously,reported
R49 T925 T924 pobj humans,in
R50 T926 T925 prep with,humans
R51 T927 T926 pobj mutation,with
R52 T928 T927 prep at,mutation
R53 T929 T930 det the,locus
R54 T930 T928 pobj locus,at
R55 T931 T930 amod same,locus
R57 T934 T935 prep Through,show
R58 T936 T937 nmod linkage,analysis
R59 T937 T934 pobj analysis,Through
R60 T938 T936 cc and,linkage
R61 T939 T936 conj sequence,linkage
R62 T940 T935 nsubj we,show
R63 T941 T935 advmod here,show
R64 T942 T943 mark that,caused
R65 T943 T935 ccomp caused,show
R66 T944 T945 det this,disorder
R67 T945 T943 nsubjpass disorder,caused
R68 T946 T943 auxpass is,caused
R69 T947 T943 agent by,caused
R70 T948 T949 det a,deletion
R71 T949 T947 pobj deletion,by
R72 T950 T949 amod homozygous,deletion
R73 T951 T949 nmod in,deletion
R74 T952 T951 punct -,in
R75 T953 T951 pobj frame,in
R76 T954 T955 nummod 18,bp
R77 T955 T949 compound bp,deletion
R78 T956 T955 punct -,bp
R79 T957 T949 prep in,deletion
R80 T958 T957 pobj Itpr1,in
R81 T959 T960 punct (,Δ18
R82 T960 T958 parataxis Δ18,Itpr1
R83 T961 T960 compound Itpr1,Δ18
R84 T962 T960 compound Δ18,Δ18
R85 T963 T960 punct /,Δ18
R86 T964 T960 punct ),Δ18
R87 T965 T949 punct ", ",deletion
R88 T966 T949 acl encoding,deletion
R89 T967 T968 nmod inositol,receptor
R90 T968 T966 dobj receptor,encoding
R91 T969 T970 nummod 1,5
R92 T970 T974 nummod 5,triphosphate
R93 T971 T970 punct ",",5
R94 T972 T970 nummod 4,5
R95 T973 T970 punct ",",5
R96 T974 T968 compound triphosphate,receptor
R97 T975 T974 punct -,triphosphate
R98 T976 T968 nummod 1,receptor
R99 T977 T935 punct .,show