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PMC:1892049 / 55-249 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
T826 21-27 NCBITaxon:9606 denotes Humans
T827 88-97 GO:0030849 denotes autosomal
T828 108-116 GO_EXT:biological_movement_or_translocation_process denotes movement
T829 129-133 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
T791 21-27 NCBITaxon:9606 denotes Humans
T792 88-97 GO:0030849 denotes autosomal
T793 129-133 NCBITaxon:10088 denotes mice

craft-sa-dev

Id Subject Object Predicate Lexical cue
T881 8-14 NN denotes Ataxia
T882 15-17 CD denotes 15
T883 18-20 IN denotes in
T884 21-27 NNS denotes Humans
T887 27-161 sentence denotes ITPR1 Deletion Causes Ataxia Abstract We observed a severe autosomal recessive movement disorder in mice used within our laboratory.
T888 67-69 PRP denotes We
T889 70-78 VBD denotes observed
T890 79-80 DT denotes a
T891 117-125 NN denotes disorder
T892 81-87 JJ denotes severe
T893 88-97 JJ denotes autosomal
T894 98-107 JJ denotes recessive
T895 108-116 NN denotes movement
T896 126-128 IN denotes in
T897 129-133 NNS denotes mice
T898 134-138 VBN denotes used
T899 139-145 IN denotes within
T900 146-149 PRP$ denotes our
T901 150-160 NN denotes laboratory
T902 160-161 . denotes .
T904 162-164 PRP denotes We
T905 165-172 VBD denotes pursued
T906 173-174 DT denotes a
T907 175-181 NN denotes series
T908 182-184 IN denotes of
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
R30 T906 T907 det a,series
R31 T907 T905 dobj series,pursued
R32 T908 T907 prep of,series

Biotea

Id Subject Object Predicate Lexical cue
T510 8-14 http://purl.bioontology.org/ontology/OMIM/MTHU036349 denotes Ataxia
T514 8-14 http://purl.obolibrary.org/obo/SYMP_0000005 denotes Ataxia
T518 8-14 http://purl.bioontology.org/ontology/MEDDRA/10003591 denotes Ataxia
T522 8-14 http://purl.bioontology.org/ontology/MEDLINEPLUS/C0004134 denotes Ataxia
T526 8-14 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C26702 denotes Ataxia
T530 8-14 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C146737 denotes Ataxia
T534 8-14 http://purl.bioontology.org/ontology/SNOMEDCT/20262006 denotes Ataxia
T538 8-14 http://purl.bioontology.org/ontology/MESH/D001259 denotes Ataxia
T542 129-133 http://purl.obolibrary.org/obo/PR_O89094 denotes mice
T546 129-133 http://purl.obolibrary.org/obo/PR_000005054 denotes mice
T550 129-133 http://purl.bioontology.org/ontology/MESH/D051379 denotes mice
T554 129-133 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C14238 denotes mice
T572 21-27 http://purl.bioontology.org/ontology/MESH/D006801 denotes Humans
T575 70-78 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C25599 denotes observed
T577 81-87 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C121395 denotes severe
T578 81-87 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C122951 denotes severe
T579 81-87 http://purl.bioontology.org/ontology/SNOMEDCT/24484000 denotes severe
T580 81-87 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C41340 denotes severe
T581 81-87 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C156244 denotes severe
T582 81-87 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C70667 denotes severe
T583 88-107 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C94246 denotes autosomal recessive
T584 88-107 http://purl.bioontology.org/ontology/SNOMEDCT/258211005 denotes autosomal recessive
T585 88-107 http://purl.bioontology.org/ontology/OMIM/MTHU000016 denotes autosomal recessive
T586 88-97 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C32168 denotes autosomal
T588 108-125 http://purl.bioontology.org/ontology/OMIM/MTHU044333 denotes movement disorder
T589 108-125 http://purl.bioontology.org/ontology/MEDDRA/10028035 denotes movement disorder
T590 108-125 http://purl.bioontology.org/ontology/SNOMEDCT/60342002 denotes movement disorder
T591 108-125 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C116757 denotes movement disorder
T592 108-116 http://purl.bioontology.org/ontology/MESH/D009068 denotes movement
T593 108-116 http://purl.bioontology.org/ontology/OMIM/MTHU000756 denotes movement
T594 108-116 http://purl.bioontology.org/ontology/SNOMEDCT/255324009 denotes movement
T595 108-116 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C37994 denotes movement
T596 117-125 http://purl.bioontology.org/ontology/SNOMEDCT/64572001 denotes disorder
T601 117-125 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C2991 denotes disorder
T606 150-160 http://purl.bioontology.org/ontology/SNOMEDCT/261904005 denotes laboratory
T607 150-160 http://purl.bioontology.org/ontology/MESH/D007753 denotes laboratory
T608 150-160 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C37984 denotes laboratory
T609 175-181 http://purl.bioontology.org/ontology/SNOMEDCT/13039001 denotes series
T611 175-181 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C25674 denotes series
T613 175-181 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C69225 denotes series