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PMC:1892049 / 7151-7419 JSONTXT 5 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue
T6945 3-5 IN denotes to
T6946 6-9 DT denotes the
T6948 10-18 JJ denotes syntenic
T6947 19-25 NN denotes region
T6949 26-28 IN denotes of
T6950 29-32 DT denotes the
T6952 33-38 JJ denotes human
T6951 39-45 NN denotes genome
T6953 45-47 , denotes ,
T6954 47-50 CC denotes but
T6955 51-56 WRB denotes where
T6957 57-59 DT denotes no
T6959 60-66 JJ denotes causal
T6958 67-75 NN denotes mutation
T6960 76-79 VBD denotes had
T6961 80-84 VBN denotes been
T6956 85-95 VBN denotes identified
T6962 95-96 . denotes .
T6963 96-185 sentence denotes SCA15, an adult-onset autosomal dominant progressive ataxia is linked to this locus [5].
T6964 97-102 NN denotes SCA15
T6966 102-104 , denotes ,
T6967 104-106 DT denotes an
T6969 107-112 JJ denotes adult
T6971 112-113 HYPH denotes -
T6970 113-118 NN denotes onset
T6972 119-128 JJ denotes autosomal
T6973 129-137 JJ denotes dominant
T6974 138-149 JJ denotes progressive
T6968 150-156 NN denotes ataxia
T6975 157-159 VBZ denotes is
T6965 160-166 VBN denotes linked
T6976 167-169 IN denotes to
T6977 170-174 DT denotes this
T6978 175-180 NN denotes locus
T6979 181-182 -LRB- denotes [
T6980 182-183 CD denotes 5
T6981 183-184 -RRB- denotes ]
T6982 184-185 . denotes .
T6984 186-194 IN denotes Although
T6986 195-203 NN denotes missense
T6987 204-212 NN denotes mutation
T6988 213-215 IN denotes of
T6989 216-221 NN denotes ITPR1
T6990 222-225 VBD denotes had
T6991 226-236 RB denotes previously
T6992 237-241 VBN denotes been
T6985 242-247 VBN denotes ruled
T6994 248-251 RP denotes out
T6995 252-253 -LRB- denotes [
T6996 253-254 CD denotes 2
T6997 254-255 -RRB- denotes ]
T6998 256-259 CC denotes and
T6999 260-263 DT denotes the
T7000 264-268 NN denotes mode
R894 T6946 T6947 det the,region
R895 T6947 T6945 pobj region,to
R896 T6948 T6947 amod syntenic,region
R898 T6949 T6947 prep of,region
R899 T6950 T6951 det the,genome
R900 T6951 T6949 pobj genome,of
R902 T6952 T6951 amod human,genome
R906 T6955 T6956 advmod where,identified
R909 T6957 T6958 det no,mutation
R910 T6958 T6956 nsubjpass mutation,identified
R911 T6959 T6958 amod causal,mutation
R913 T6960 T6956 aux had,identified
R914 T6961 T6956 auxpass been,identified
R917 T6964 T6965 nsubjpass SCA15,linked
R918 T6966 T6964 punct ", ",SCA15
R919 T6967 T6968 det an,ataxia
R920 T6968 T6964 appos ataxia,SCA15
R921 T6969 T6970 amod adult,onset
R922 T6970 T6968 nmod onset,ataxia
R924 T6971 T6970 punct -,onset
R925 T6972 T6973 amod autosomal,dominant
R926 T6973 T6968 amod dominant,ataxia
R928 T6974 T6968 amod progressive,ataxia
R929 T6975 T6965 auxpass is,linked
R930 T6976 T6965 prep to,linked
R932 T6977 T6978 det this,locus
R933 T6978 T6976 pobj locus,to
R935 T6979 T6980 punct [,5
R936 T6980 T6965 parataxis 5,linked
R938 T6981 T6980 punct ],5
R939 T6982 T6965 punct .,linked
R941 T6984 T6985 mark Although,ruled
R943 T6986 T6987 compound missense,mutation
R945 T6987 T6985 nsubjpass mutation,ruled
R946 T6988 T6987 prep of,mutation
R947 T6989 T6988 pobj ITPR1,of
R949 T6990 T6985 aux had,ruled
R950 T6991 T6985 advmod previously,ruled
R951 T6992 T6985 auxpass been,ruled
R953 T6994 T6985 prt out,ruled
R954 T6995 T6996 punct [,2
R956 T6996 T6985 parataxis 2,ruled
R957 T6997 T6996 punct ],2
R958 T6998 T6985 cc and,ruled
R960 T6999 T7000 det the,mode