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PMC:1584416 / 4409-4628 JSONTXT

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craft-sa-dev

Id Subject Object Predicate Lexical cue
T1003 81-90 VBN denotes described
T1012 1-4 DT denotes the
T1013 24-37 NNS denotes complications
T1014 5-23 JJ denotes neurodevelopmental
T1015 38-40 IN denotes of
T1016 41-43 NN denotes CS
T1017 44-45 -LRB- denotes (
T1018 45-49 NN denotes XPCS
T1019 49-50 -RRB- denotes )
T1020 50-52 , denotes ,
T1021 52-60 IN denotes although
T1022 61-65 JJ denotes rare
T1023 65-67 , denotes ,
T1024 67-70 VBZ denotes has
T1025 71-75 RB denotes also
T1026 76-80 VBN denotes been
T1027 91-92 -LRB- denotes [
T1028 92-94 CD denotes 18
T1029 94-95 -RRB- denotes ]
T1030 95-96 . denotes .
T1032 97-101 JJ denotes Many
T1033 106-115 NNS denotes mutations
T1034 102-105 NN denotes XPD
T1035 120-130 VBN denotes associated
T1036 116-119 VBP denotes are
T1037 131-135 IN denotes with
T1038 136-138 DT denotes an
T1039 157-166 NN denotes phenotype
T1040 139-148 JJ denotes exclusive
T1041 149-156 NN denotes disease
T1042 167-168 -LRB- denotes (
T1043 174-182 NN denotes XPDR722W
T1044 168-172 FW denotes e.g.
T1045 172-174 , denotes ,
T1046 183-187 IN denotes with
T1047 188-191 NN denotes TTD
T1048 192-195 CC denotes and
T1049 196-204 NN denotes XPDR683W
T1050 205-209 IN denotes with
T1051 210-212 NN denotes XP
T1052 212-213 -RRB- denotes )
T1053 214-217 CC denotes and
R668 T1012 T1013 det the,complications
R670 T1014 T1013 amod neurodevelopmental,complications
R671 T1015 T1013 prep of,complications
R672 T1016 T1015 pobj CS,of
R673 T1017 T1018 punct (,XPCS
R674 T1018 T1016 parataxis XPCS,CS
R675 T1019 T1018 punct ),XPCS
R676 T1020 T1003 punct ", ",described
R677 T1021 T1022 mark although,rare
R678 T1022 T1003 advcl rare,described
R679 T1023 T1003 punct ", ",described
R680 T1024 T1003 aux has,described
R681 T1025 T1003 advmod also,described
R682 T1026 T1003 auxpass been,described
R683 T1027 T1028 punct [,18
R684 T1028 T1003 parataxis 18,described
R685 T1029 T1028 punct ],18
R686 T1030 T1003 punct .,described
R687 T1032 T1033 amod Many,mutations
R689 T1034 T1033 compound XPD,mutations
R690 T1036 T1035 auxpass are,associated
R691 T1037 T1035 prep with,associated
R692 T1038 T1039 det an,phenotype
R693 T1039 T1037 pobj phenotype,with
R694 T1040 T1039 amod exclusive,phenotype
R695 T1041 T1039 compound disease,phenotype
R696 T1042 T1043 punct (,XPDR722W
R697 T1043 T1039 parataxis XPDR722W,phenotype
R698 T1044 T1043 advmod e.g.,XPDR722W
R699 T1045 T1043 punct ", ",XPDR722W
R700 T1046 T1043 prep with,XPDR722W
R701 T1047 T1046 pobj TTD,with
R702 T1048 T1043 cc and,XPDR722W
R703 T1049 T1043 conj XPDR683W,XPDR722W
R704 T1050 T1049 prep with,XPDR683W
R705 T1051 T1050 pobj XP,with
R706 T1052 T1043 punct ),XPDR722W
R707 T1053 T1035 cc and,associated
R688 T1033 T1035 nsubjpass mutations,associated

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
T443 5-23 GO:0007399 denotes neurodevelopmental
T444 102-105 PR:000007164 denotes XPD
T445 174-177 PR:000007164 denotes XPD
T446 196-199 PR:000007164 denotes XPD

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
T533 5-23 GO:0007399 denotes neurodevelopmental
T534 102-105 PR_EXT:000007164 denotes XPD
T535 106-115 SO_EXT:sequence_alteration_entity_or_process denotes mutations
T536 174-177 PR_EXT:000007164 denotes XPD
T537 196-199 PR_EXT:000007164 denotes XPD

2_test

Id Subject Object Predicate Lexical cue
17020410-15226750-84795132 92-94 15226750 denotes 18
T90963 92-94 15226750 denotes 18