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PMC:1892049 / 14853-15043 JSONTXT

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craft-ca-core-ex-dev

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

Id Subject Object Predicate Lexical cue
T6254 12-20 SO_EXT:sequence_alteration_entity_or_process denotes mutation
T6255 24-29 PR_EXT:000015827 denotes SUMF1
T6256 41-50 GO:0030849 denotes autosomal
T6257 70-79 GO_EXT:0008484 denotes sulfatase
T6258 94-103 GO:0008152 denotes metabolic

craft-ca-core-dev

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

Id Subject Object Predicate Lexical cue
T5950 24-29 PR:000015827 denotes SUMF1
T5951 41-50 GO:0030849 denotes autosomal
T5952 94-103 GO:0008152 denotes metabolic

craft-sa-dev

Id Subject Object Predicate Lexical cue
T7948 0-190 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 1-11 JJ denotes Homozygous
T7950 12-20 NN denotes mutation
T7951 30-37 VBZ denotes results
T7952 21-23 IN denotes of
T7953 24-29 NN denotes SUMF1
T7954 38-40 IN denotes in
T7955 41-50 JJ denotes autosomal
T7956 80-90 NN denotes deficiency
T7957 51-60 JJ denotes recessive
T7958 61-69 JJ denotes multiple
T7959 70-79 NN denotes sulfatase
T7960 90-92 , denotes ,
T7961 92-93 DT denotes a
T7962 104-112 NN denotes disorder
T7963 94-103 JJ denotes metabolic
T7964 113-126 VBN denotes characterized
T7965 127-129 IN denotes by
T7966 130-148 NN denotes hepatosplenomegaly
T7967 148-150 , denotes ,
T7968 150-158 NN denotes deafness
T7969 158-160 , denotes ,
T7970 160-163 CC denotes and
T7971 164-177 JJ denotes developmental
T7972 178-183 NN denotes delay
T7973 184-185 -LRB- denotes [
T7974 187-188 CD denotes 7
T7975 185-186 CD denotes 6
T7976 186-187 , denotes ,
T7977 188-189 -RRB- denotes ]
T7978 189-190 . denotes .
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
R1936 T7949 T7950 amod Homozygous,mutation
R1937 T7950 T7951 nsubj mutation,results
R1939 T7952 T7950 prep of,mutation
R1941 T7953 T7952 pobj SUMF1,of
R1942 T7954 T7951 prep in,results
R1943 T7955 T7956 amod autosomal,deficiency
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 185-186 12757706 denotes 6
17590087-15146462-85657853 187-188 15146462 denotes 7
T64473 185-186 12757706 denotes 6
T55562 187-188 15146462 denotes 7