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PMC:1892049 / 129-291 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
T827 14-23 GO:0030849 denotes autosomal
T828 34-42 GO_EXT:biological_movement_or_translocation_process denotes movement
T829 55-59 NCBITaxon:10088 denotes mice
T830 137-144 SO_EXT:0000704 denotes genetic

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
T792 14-23 GO:0030849 denotes autosomal
T793 55-59 NCBITaxon:10088 denotes mice
T794 137-144 SO:0000704 denotes genetic

craft-sa-dev

Id Subject Object Predicate Lexical cue
T890 5-6 DT denotes a
T891 43-51 NN denotes disorder
T892 7-13 JJ denotes severe
T893 14-23 JJ denotes autosomal
T894 24-33 JJ denotes recessive
T895 34-42 NN denotes movement
T896 52-54 IN denotes in
T897 55-59 NNS denotes mice
T898 60-64 VBN denotes used
T899 65-71 IN denotes within
T900 72-75 PRP$ denotes our
T901 76-86 NN denotes laboratory
T902 86-87 . denotes .
T904 88-90 PRP denotes We
T905 91-98 VBD denotes pursued
T906 99-100 DT denotes a
T907 101-107 NN denotes series
T908 108-110 IN denotes of
T909 111-122 NNS denotes experiments
T910 123-125 TO denotes to
T911 126-132 VB denotes define
T912 133-136 DT denotes the
T913 145-151 NN denotes lesion
T914 137-144 JJ denotes genetic
T915 152-162 VBG denotes underlying
R16 T890 T891 det a,disorder
R18 T892 T891 amod severe,disorder
R19 T893 T891 amod autosomal,disorder
R20 T894 T891 amod recessive,disorder
R21 T895 T891 compound movement,disorder
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
R29 T904 T905 nsubj We,pursued
R30 T906 T907 det a,series
R31 T907 T905 dobj series,pursued
R32 T908 T907 prep of,series
R33 T909 T908 pobj experiments,of
R34 T910 T911 aux to,define
R35 T911 T905 advcl define,pursued
R36 T912 T913 det the,lesion
R37 T913 T911 dobj lesion,define
R38 T914 T913 amod genetic,lesion
R39 T915 T913 acl underlying,lesion

Biotea

Id Subject Object Predicate Lexical cue
T542 55-59 http://purl.obolibrary.org/obo/PR_O89094 denotes mice
T546 55-59 http://purl.obolibrary.org/obo/PR_000005054 denotes mice
T550 55-59 http://purl.bioontology.org/ontology/MESH/D051379 denotes mice
T554 55-59 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C14238 denotes mice
T577 7-13 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C121395 denotes severe
T578 7-13 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C122951 denotes severe
T579 7-13 http://purl.bioontology.org/ontology/SNOMEDCT/24484000 denotes severe
T580 7-13 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C41340 denotes severe
T581 7-13 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C156244 denotes severe
T582 7-13 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C70667 denotes severe
T583 14-33 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C94246 denotes autosomal recessive
T584 14-33 http://purl.bioontology.org/ontology/SNOMEDCT/258211005 denotes autosomal recessive
T585 14-33 http://purl.bioontology.org/ontology/OMIM/MTHU000016 denotes autosomal recessive
T586 14-23 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C32168 denotes autosomal
T588 34-51 http://purl.bioontology.org/ontology/OMIM/MTHU044333 denotes movement disorder
T589 34-51 http://purl.bioontology.org/ontology/MEDDRA/10028035 denotes movement disorder
T590 34-51 http://purl.bioontology.org/ontology/SNOMEDCT/60342002 denotes movement disorder
T591 34-51 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C116757 denotes movement disorder
T592 34-42 http://purl.bioontology.org/ontology/MESH/D009068 denotes movement
T593 34-42 http://purl.bioontology.org/ontology/OMIM/MTHU000756 denotes movement
T594 34-42 http://purl.bioontology.org/ontology/SNOMEDCT/255324009 denotes movement
T595 34-42 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C37994 denotes movement
T596 43-51 http://purl.bioontology.org/ontology/SNOMEDCT/64572001 denotes disorder
T601 43-51 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C2991 denotes disorder
T606 76-86 http://purl.bioontology.org/ontology/SNOMEDCT/261904005 denotes laboratory
T607 76-86 http://purl.bioontology.org/ontology/MESH/D007753 denotes laboratory
T608 76-86 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C37984 denotes laboratory
T609 101-107 http://purl.bioontology.org/ontology/SNOMEDCT/13039001 denotes series
T611 101-107 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C25674 denotes series
T613 101-107 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C69225 denotes series
T615 126-132 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C142506 denotes define
T616 137-144 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C15238 denotes genetic
T617 137-144 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C17938 denotes genetic
T618 145-151 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C71163 denotes lesion
T619 145-151 http://purl.bioontology.org/ontology/SNOMEDCT/52988006 denotes lesion
T620 145-151 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C3824 denotes lesion
T621 152-162 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C154417 denotes underlying