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PMC:1892049 / 28-234 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
T824 10-14 NCBITaxon:10088 denotes Mice
T825 19-34 UBERON:0014643 denotes Spinocerebellar
T826 48-54 NCBITaxon:9606 denotes Humans
T827 115-124 GO:0030849 denotes autosomal
T828 135-143 GO_EXT:biological_movement_or_translocation_process denotes movement
T829 156-160 NCBITaxon:10088 denotes mice

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
T789 10-14 NCBITaxon:10088 denotes Mice
T790 19-34 UBERON:0014643 denotes Spinocerebellar
T791 48-54 NCBITaxon:9606 denotes Humans
T792 115-124 GO:0030849 denotes autosomal
T793 156-160 NCBITaxon:10088 denotes mice

craft-sa-dev

Id Subject Object Predicate Lexical cue
T876 0-6 NN denotes Ataxia
T877 7-9 IN denotes in
T878 10-14 NNS denotes Mice
T879 15-18 CC denotes and
T880 19-34 JJ denotes Spinocerebellar
T881 35-41 NN denotes Ataxia
T882 42-44 CD denotes 15
T883 45-47 IN denotes in
T884 48-54 NNS denotes Humans
T887 54-188 sentence denotes ITPR1 Deletion Causes Ataxia Abstract We observed a severe autosomal recessive movement disorder in mice used within our laboratory.
T888 94-96 PRP denotes We
T889 97-105 VBD denotes observed
T890 106-107 DT denotes a
T891 144-152 NN denotes disorder
T892 108-114 JJ denotes severe
T893 115-124 JJ denotes autosomal
T894 125-134 JJ denotes recessive
T895 135-143 NN denotes movement
T896 153-155 IN denotes in
T897 156-160 NNS denotes mice
T898 161-165 VBN denotes used
T899 166-172 IN denotes within
T900 173-176 PRP$ denotes our
T901 177-187 NN denotes laboratory
T902 187-188 . denotes .
T904 189-191 PRP denotes We
T905 192-199 VBD denotes pursued
T906 200-201 DT denotes a
R7 T877 T876 prep in,Ataxia
R8 T878 T877 pobj Mice,in
R9 T879 T876 cc and,Ataxia
R10 T880 T881 amod Spinocerebellar,Ataxia
R11 T881 T876 conj Ataxia,Ataxia
R12 T882 T881 nummod 15,Ataxia
R13 T883 T881 prep in,Ataxia
R14 T884 T883 pobj Humans,in
R15 T888 T889 nsubj We,observed
R16 T890 T891 det a,disorder
R17 T891 T889 dobj disorder,observed
R18 T892 T891 amod severe,disorder
R19 T893 T891 amod autosomal,disorder
R20 T894 T891 amod recessive,disorder
R21 T895 T891 compound movement,disorder
R22 T896 T889 prep in,observed
R23 T897 T896 pobj mice,in
R24 T898 T897 acl used,mice
R25 T899 T898 prep within,used
R26 T900 T901 poss our,laboratory
R27 T901 T899 pobj laboratory,within
R28 T902 T889 punct .,observed
R29 T904 T905 nsubj We,pursued

Biotea

Id Subject Object Predicate Lexical cue
T510 35-41 http://purl.bioontology.org/ontology/OMIM/MTHU036349 denotes Ataxia
T513 0-6 http://purl.obolibrary.org/obo/SYMP_0000005 denotes Ataxia
T514 35-41 http://purl.obolibrary.org/obo/SYMP_0000005 denotes Ataxia
T517 0-6 http://purl.bioontology.org/ontology/MEDDRA/10003591 denotes Ataxia
T518 35-41 http://purl.bioontology.org/ontology/MEDDRA/10003591 denotes Ataxia
T521 0-6 http://purl.bioontology.org/ontology/MEDLINEPLUS/C0004134 denotes Ataxia
T522 35-41 http://purl.bioontology.org/ontology/MEDLINEPLUS/C0004134 denotes Ataxia
T525 0-6 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C26702 denotes Ataxia
T526 35-41 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C26702 denotes Ataxia
T529 0-6 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C146737 denotes Ataxia
T530 35-41 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C146737 denotes Ataxia
T533 0-6 http://purl.bioontology.org/ontology/SNOMEDCT/20262006 denotes Ataxia
T534 35-41 http://purl.bioontology.org/ontology/SNOMEDCT/20262006 denotes Ataxia
T537 0-6 http://purl.bioontology.org/ontology/MESH/D001259 denotes Ataxia
T538 35-41 http://purl.bioontology.org/ontology/MESH/D001259 denotes Ataxia
T541 10-14 http://purl.obolibrary.org/obo/PR_O89094 denotes Mice
T542 156-160 http://purl.obolibrary.org/obo/PR_O89094 denotes mice
T545 10-14 http://purl.obolibrary.org/obo/PR_000005054 denotes Mice
T546 156-160 http://purl.obolibrary.org/obo/PR_000005054 denotes mice
T549 10-14 http://purl.bioontology.org/ontology/MESH/D051379 denotes Mice
T550 156-160 http://purl.bioontology.org/ontology/MESH/D051379 denotes mice
T553 10-14 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C14238 denotes Mice
T554 156-160 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C14238 denotes mice
T557 19-44 http://purl.bioontology.org/ontology/MESH/C564685 denotes Spinocerebellar Ataxia 15
T559 19-44 http://purl.bioontology.org/ontology/OMIM/606658 denotes Spinocerebellar Ataxia 15
T564 19-41 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C82341 denotes Spinocerebellar Ataxia
T566 19-41 http://purl.bioontology.org/ontology/MEDDRA/10057660 denotes Spinocerebellar Ataxia
T568 19-41 http://purl.bioontology.org/ontology/OMIM/MTHU004242 denotes Spinocerebellar Ataxia
T570 19-41 http://purl.bioontology.org/ontology/SNOMEDCT/129609000 denotes Spinocerebellar Ataxia
T572 48-54 http://purl.bioontology.org/ontology/MESH/D006801 denotes Humans
T575 97-105 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C25599 denotes observed
T577 108-114 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C121395 denotes severe
T578 108-114 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C122951 denotes severe
T579 108-114 http://purl.bioontology.org/ontology/SNOMEDCT/24484000 denotes severe
T580 108-114 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C41340 denotes severe
T581 108-114 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C156244 denotes severe
T582 108-114 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C70667 denotes severe
T583 115-134 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C94246 denotes autosomal recessive
T584 115-134 http://purl.bioontology.org/ontology/SNOMEDCT/258211005 denotes autosomal recessive
T585 115-134 http://purl.bioontology.org/ontology/OMIM/MTHU000016 denotes autosomal recessive
T586 115-124 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C32168 denotes autosomal
T588 135-152 http://purl.bioontology.org/ontology/OMIM/MTHU044333 denotes movement disorder
T589 135-152 http://purl.bioontology.org/ontology/MEDDRA/10028035 denotes movement disorder
T590 135-152 http://purl.bioontology.org/ontology/SNOMEDCT/60342002 denotes movement disorder
T591 135-152 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C116757 denotes movement disorder
T592 135-143 http://purl.bioontology.org/ontology/MESH/D009068 denotes movement
T593 135-143 http://purl.bioontology.org/ontology/OMIM/MTHU000756 denotes movement
T594 135-143 http://purl.bioontology.org/ontology/SNOMEDCT/255324009 denotes movement
T595 135-143 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C37994 denotes movement
T596 144-152 http://purl.bioontology.org/ontology/SNOMEDCT/64572001 denotes disorder
T601 144-152 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C2991 denotes disorder
T606 177-187 http://purl.bioontology.org/ontology/SNOMEDCT/261904005 denotes laboratory
T607 177-187 http://purl.bioontology.org/ontology/MESH/D007753 denotes laboratory
T608 177-187 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C37984 denotes laboratory
T509 0-6 http://purl.bioontology.org/ontology/OMIM/MTHU036349 denotes Ataxia