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PMC:1892049 / 14818-15142 JSONTXT

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craft-ca-core-ex-dev

Below, discontinuous spans are shown in the bag model. You can change it to the chain model.

Id Subject Object Predicate Lexical cue
T6254 47-55 SO_EXT:sequence_alteration_entity_or_process denotes mutation
T6255 59-64 PR_EXT:000015827 denotes SUMF1
T6256 76-85 GO:0030849 denotes autosomal
T6257 105-114 GO_EXT:0008484 denotes sulfatase
T6258 129-138 GO:0008152 denotes metabolic

craft-ca-core-dev

Below, discontinuous spans are shown in the bag model. You can change it to the chain model.

Id Subject Object Predicate Lexical cue
T5950 59-64 PR:000015827 denotes SUMF1
T5951 76-85 GO:0030849 denotes autosomal
T5952 129-138 GO:0008152 denotes metabolic

craft-sa-dev

Id Subject Object Predicate Lexical cue
T7927 4-10 VBZ denotes causes
T7943 11-13 CC denotes or
T7944 14-25 VBZ denotes contributes
T7945 26-28 IN denotes to
T7946 29-34 NN denotes SCA15
T7947 34-35 . denotes .
T7948 35-225 sentence denotes Homozygous mutation of SUMF1 results in autosomal recessive multiple sulfatase deficiency, a metabolic disorder characterized by hepatosplenomegaly, deafness, and developmental delay [6,7].
T7949 36-46 JJ denotes Homozygous
T7950 47-55 NN denotes mutation
T7951 65-72 VBZ denotes results
T7952 56-58 IN denotes of
T7953 59-64 NN denotes SUMF1
T7954 73-75 IN denotes in
T7955 76-85 JJ denotes autosomal
T7956 115-125 NN denotes deficiency
T7957 86-95 JJ denotes recessive
T7958 96-104 JJ denotes multiple
T7959 105-114 NN denotes sulfatase
T7960 125-127 , denotes ,
T7961 127-128 DT denotes a
T7962 139-147 NN denotes disorder
T7963 129-138 JJ denotes metabolic
T7964 148-161 VBN denotes characterized
T7965 162-164 IN denotes by
T7966 165-183 NN denotes hepatosplenomegaly
T7967 183-185 , denotes ,
T7968 185-193 NN denotes deafness
T7969 193-195 , denotes ,
T7970 195-198 CC denotes and
T7971 199-212 JJ denotes developmental
T7972 213-218 NN denotes delay
T7973 219-220 -LRB- denotes [
T7974 222-223 CD denotes 7
T7975 220-221 CD denotes 6
T7976 221-222 , denotes ,
T7977 223-224 -RRB- denotes ]
T7978 224-225 . denotes .
T7980 226-228 DT denotes No
T7981 229-242 NN denotes co-occurrence
T7982 262-271 VBN denotes described
T7983 243-245 IN denotes of
T7984 246-252 NN denotes ataxia
T7985 253-256 VBZ denotes has
T7986 257-261 VBN denotes been
T7987 272-274 IN denotes in
T7988 275-276 -LRB- denotes (
T7989 290-297 NNS denotes parents
T7990 276-288 JJ denotes heterozygous
T7991 288-289 -RRB- denotes )
T7992 298-300 IN denotes of
T7993 301-309 NNS denotes patients
T7994 310-314 IN denotes with
T7995 315-323 JJ denotes multiple
R1821 T7959 T7956 compound sulfatase,deficiency
R1827 T7960 T7956 punct ", ",deficiency
R1831 T7961 T7962 det a,disorder
R1833 T7962 T7956 appos disorder,deficiency
R1837 T7963 T7962 amod metabolic,disorder
R1838 T7964 T7962 acl characterized,disorder
R1840 T7965 T7964 agent by,characterized
R1843 T7966 T7965 pobj hepatosplenomegaly,by
R1846 T7967 T7966 punct ", ",hepatosplenomegaly
R1850 T7968 T7966 conj deafness,hepatosplenomegaly
R1857 T7969 T7968 punct ", ",deafness
R1861 T7970 T7968 cc and,deafness
R1865 T7971 T7972 amod developmental,delay
R1869 T7972 T7968 conj delay,deafness
R1872 T7973 T7974 punct [,7
R1876 T7974 T7951 parataxis 7,results
R1880 T7975 T7974 nummod 6,7
R1883 T7976 T7974 punct ",",7
R1887 T7977 T7974 punct ],7
R1891 T7978 T7951 punct .,results
R1895 T7980 T7981 det No,co-occurrence
R1900 T7981 T7982 nsubjpass co-occurrence,described
R1903 T7983 T7981 prep of,co-occurrence
R1909 T7984 T7983 pobj ataxia,of
R1912 T7985 T7982 aux has,described
R1917 T7986 T7982 auxpass been,described
R1920 T7987 T7982 prep in,described
R1924 T7988 T7989 punct (,parents
R1928 T7989 T7987 pobj parents,in
R1929 T7943 T7927 cc or,causes
R1930 T7944 T7927 conj contributes,causes
R1931 T7990 T7989 amod heterozygous,parents
R1932 T7945 T7944 prep to,contributes
R1933 T7946 T7944 dobj SCA15,contributes
R1935 T7991 T7989 punct ),parents
R1936 T7949 T7950 amod Homozygous,mutation
R1937 T7950 T7951 nsubj mutation,results
R1938 T7992 T7989 prep of,parents
R1939 T7952 T7950 prep of,mutation
R1940 T7993 T7992 pobj patients,of
R1941 T7953 T7952 pobj SUMF1,of
R1942 T7954 T7951 prep in,results
R1943 T7955 T7956 amod autosomal,deficiency
R1944 T7994 T7993 prep with,patients
R1946 T7956 T7954 pobj deficiency,in
R1947 T7957 T7956 amod recessive,deficiency
R1949 T7958 T7956 amod multiple,deficiency

2_test

Id Subject Object Predicate Lexical cue
17590087-12757706-85657852 220-221 12757706 denotes 6
17590087-15146462-85657853 222-223 15146462 denotes 7
T64473 220-221 12757706 denotes 6
T55562 222-223 15146462 denotes 7