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PMC:1892049 / 814-985 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
T853 8-13 CL_GO_EXT:cell denotes cells
T854 15-30 UBERON:0014643 denotes Spinocerebellar
T855 52-57 NCBITaxon:9606 denotes human
T856 58-67 GO:0030849 denotes autosomal
T857 99-106 SO_EXT:0001026 denotes genomic
T858 125-130 PR_EXT:000009158 denotes ITPR1
T859 159-168 SO_EXT:sequence_alteration_entity_or_process denotes mutations

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
T809 15-30 UBERON:0014643 denotes Spinocerebellar
T810 52-57 NCBITaxon:9606 denotes human
T811 58-67 GO:0030849 denotes autosomal
T812 99-106 SO:0001026 denotes genomic
T813 125-130 PR:000009158 denotes ITPR1

craft-sa-dev

Id Subject Object Predicate Lexical cue
T1020 8-13 NNS denotes cells
T1022 13-14 . denotes .
T1024 15-30 JJ denotes Spinocerebellar
T1025 31-37 NN denotes ataxia
T1026 87-91 VBZ denotes maps
T1027 38-40 CD denotes 15
T1028 41-42 -LRB- denotes (
T1029 42-47 NN denotes SCA15
T1030 47-48 -RRB- denotes )
T1031 48-50 , denotes ,
T1032 50-51 DT denotes a
T1033 77-85 NN denotes disorder
T1034 52-57 JJ denotes human
T1035 58-67 JJ denotes autosomal
T1036 68-76 JJ denotes dominant
T1037 85-87 , denotes ,
T1039 92-94 IN denotes to
T1040 95-98 DT denotes the
T1041 107-113 NN denotes region
T1042 99-106 JJ denotes genomic
T1043 114-124 VBG denotes containing
T1044 125-130 NN denotes ITPR1
T1045 130-131 : denotes ;
T1046 132-139 RB denotes however
T1047 139-141 , denotes ,
T1048 141-143 IN denotes to
T1049 144-148 NN denotes date
T1050 149-151 DT denotes no
T1051 159-168 NNS denotes mutations
T1052 152-158 JJ denotes causal
R141 T1024 T1025 amod Spinocerebellar,ataxia
R142 T1025 T1026 nsubj ataxia,maps
R144 T1027 T1025 nummod 15,ataxia
R145 T1028 T1025 punct (,ataxia
R146 T1029 T1025 appos SCA15,ataxia
R147 T1030 T1025 punct ),ataxia
R148 T1031 T1025 punct ", ",ataxia
R149 T1032 T1033 det a,disorder
R151 T1034 T1033 amod human,disorder
R152 T1035 T1033 amod autosomal,disorder
R153 T1036 T1033 amod dominant,disorder
R154 T1037 T1026 punct ", ",maps
R155 T1039 T1026 prep to,maps
R156 T1040 T1041 det the,region
R157 T1041 T1039 pobj region,to
R158 T1042 T1041 amod genomic,region
R159 T1043 T1041 acl containing,region
R160 T1044 T1043 dobj ITPR1,containing
R165 T1049 T1048 pobj date,to
R166 T1050 T1051 det no,mutations
R168 T1052 T1051 amod causal,mutations
R150 T1033 T1025 appos disorder,ataxia

Biotea

Id Subject Object Predicate Lexical cue
T511 31-37 http://purl.bioontology.org/ontology/OMIM/MTHU036349 denotes ataxia
T515 31-37 http://purl.obolibrary.org/obo/SYMP_0000005 denotes ataxia
T519 31-37 http://purl.bioontology.org/ontology/MEDDRA/10003591 denotes ataxia
T523 31-37 http://purl.bioontology.org/ontology/MEDLINEPLUS/C0004134 denotes ataxia
T527 31-37 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C26702 denotes ataxia
T531 31-37 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C146737 denotes ataxia
T535 31-37 http://purl.bioontology.org/ontology/SNOMEDCT/20262006 denotes ataxia
T539 31-37 http://purl.bioontology.org/ontology/MESH/D001259 denotes ataxia
T558 15-40 http://purl.bioontology.org/ontology/MESH/C564685 denotes Spinocerebellar ataxia 15
T560 15-40 http://purl.bioontology.org/ontology/OMIM/606658 denotes Spinocerebellar ataxia 15
T561 42-47 http://purl.bioontology.org/ontology/OMIM/606658 denotes SCA15
T565 15-37 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C82341 denotes Spinocerebellar ataxia
T567 15-37 http://purl.bioontology.org/ontology/MEDDRA/10057660 denotes Spinocerebellar ataxia
T569 15-37 http://purl.bioontology.org/ontology/OMIM/MTHU004242 denotes Spinocerebellar ataxia
T571 15-37 http://purl.bioontology.org/ontology/SNOMEDCT/129609000 denotes Spinocerebellar ataxia
T587 58-67 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C32168 denotes autosomal
T600 77-85 http://purl.bioontology.org/ontology/SNOMEDCT/64572001 denotes disorder
T605 77-85 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C2991 denotes disorder
T630 159-168 http://purl.bioontology.org/ontology/MESH/D009154 denotes mutations
T645 107-113 http://purl.obolibrary.org/obo/SO_0000001 denotes region
T662 42-47 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C51556 denotes SCA15
T663 125-130 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C51556 denotes ITPR1
T673 125-130 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C24527 denotes ITPR1
T682 125-130 http://purl.obolibrary.org/obo/PR_000009158 denotes ITPR1
T731 8-13 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C48938 denotes cells
T732 8-13 http://purl.bioontology.org/ontology/NDFRT/N0000184307 denotes cells
T733 8-13 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C12508 denotes cells
T734 8-13 http://purl.bioontology.org/ontology/MESH/D002477 denotes cells
T735 52-57 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C14225 denotes human
T736 52-57 http://purl.bioontology.org/ontology/STY/T016 denotes human
T737 52-57 http://purl.bioontology.org/ontology/STY/T016 denotes human
T738 52-57 http://purl.bioontology.org/ontology/STY/T016 denotes human
T739 52-57 http://purl.bioontology.org/ontology/STY/T016 denotes human
T740 52-57 http://purl.bioontology.org/ontology/STY/T016 denotes human
T741 52-57 http://purl.bioontology.org/ontology/STY/T016 denotes human
T742 52-57 http://purl.bioontology.org/ontology/STY/T016 denotes human
T743 52-57 http://purl.bioontology.org/ontology/STY/T016 denotes human
T744 52-57 http://purl.bioontology.org/ontology/STY/T016 denotes human
T745 52-57 http://purl.obolibrary.org/obo/NCBITaxon_9606 denotes human
T746 52-57 http://purl.obolibrary.org/obo/NCBITaxon_9606 denotes human
T747 58-85 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C98829 denotes autosomal dominant disorder
T748 58-76 http://purl.bioontology.org/ontology/OMIM/MTHU000018 denotes autosomal dominant
T749 58-76 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C94245 denotes autosomal dominant
T750 68-76 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C25487 denotes dominant
T751 87-91 http://purl.bioontology.org/ontology/MESH/D019532 denotes maps
T752 87-91 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C16861 denotes maps
T753 99-106 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C16629 denotes genomic
T754 107-113 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C13379 denotes region
T756 107-113 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C16632 denotes region
T757 107-113 http://purl.bioontology.org/ontology/SNOMEDCT/410673009 denotes region
T758 107-113 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C41129 denotes region