> top > docs > PMC:1892049 > spans > 114-345 > annotations

PMC:1892049 / 114-345 JSONTXT

Annnotations TAB JSON ListView MergeView

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 29-38 GO:0030849 denotes autosomal
T828 49-57 GO_EXT:biological_movement_or_translocation_process denotes movement
T829 70-74 NCBITaxon:10088 denotes mice
T830 152-159 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 29-38 GO:0030849 denotes autosomal
T793 70-74 NCBITaxon:10088 denotes mice
T794 152-159 SO:0000704 denotes genetic

craft-sa-dev

Id Subject Object Predicate Lexical cue
T888 8-10 PRP denotes We
T889 11-19 VBD denotes observed
T890 20-21 DT denotes a
T891 58-66 NN denotes disorder
T892 22-28 JJ denotes severe
T893 29-38 JJ denotes autosomal
T894 39-48 JJ denotes recessive
T895 49-57 NN denotes movement
T896 67-69 IN denotes in
T897 70-74 NNS denotes mice
T898 75-79 VBN denotes used
T899 80-86 IN denotes within
T900 87-90 PRP$ denotes our
T901 91-101 NN denotes laboratory
T902 101-102 . denotes .
T904 103-105 PRP denotes We
T905 106-113 VBD denotes pursued
T906 114-115 DT denotes a
T907 116-122 NN denotes series
T908 123-125 IN denotes of
T909 126-137 NNS denotes experiments
T910 138-140 TO denotes to
T911 141-147 VB denotes define
T912 148-151 DT denotes the
T913 160-166 NN denotes lesion
T914 152-159 JJ denotes genetic
T915 167-177 VBG denotes underlying
T916 178-182 DT denotes this
T917 183-191 NN denotes disorder
T918 192-195 CC denotes and
T919 196-198 TO denotes to
T920 199-207 VB denotes identify
T921 208-209 DT denotes a
T922 218-225 NN denotes disease
T923 210-217 JJ denotes cognate
T924 226-228 IN denotes 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
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
R40 T916 T917 det this,disorder
R41 T917 T915 dobj disorder,underlying
R42 T918 T911 cc and,define
R43 T919 T920 aux to,identify
R44 T920 T911 conj identify,define
R45 T921 T922 det a,disease
R46 T922 T920 dobj disease,identify
R47 T923 T922 amod cognate,disease
R48 T924 T920 prep in,identify

Biotea

Id Subject Object Predicate Lexical cue
T542 70-74 http://purl.obolibrary.org/obo/PR_O89094 denotes mice
T546 70-74 http://purl.obolibrary.org/obo/PR_000005054 denotes mice
T550 70-74 http://purl.bioontology.org/ontology/MESH/D051379 denotes mice
T554 70-74 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C14238 denotes mice
T575 11-19 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C25599 denotes observed
T577 22-28 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C121395 denotes severe
T578 22-28 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C122951 denotes severe
T579 22-28 http://purl.bioontology.org/ontology/SNOMEDCT/24484000 denotes severe
T580 22-28 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C41340 denotes severe
T581 22-28 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C156244 denotes severe
T582 22-28 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C70667 denotes severe
T583 29-48 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C94246 denotes autosomal recessive
T584 29-48 http://purl.bioontology.org/ontology/SNOMEDCT/258211005 denotes autosomal recessive
T585 29-48 http://purl.bioontology.org/ontology/OMIM/MTHU000016 denotes autosomal recessive
T586 29-38 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C32168 denotes autosomal
T588 49-66 http://purl.bioontology.org/ontology/OMIM/MTHU044333 denotes movement disorder
T589 49-66 http://purl.bioontology.org/ontology/MEDDRA/10028035 denotes movement disorder
T590 49-66 http://purl.bioontology.org/ontology/SNOMEDCT/60342002 denotes movement disorder
T591 49-66 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C116757 denotes movement disorder
T592 49-57 http://purl.bioontology.org/ontology/MESH/D009068 denotes movement
T593 49-57 http://purl.bioontology.org/ontology/OMIM/MTHU000756 denotes movement
T594 49-57 http://purl.bioontology.org/ontology/SNOMEDCT/255324009 denotes movement
T595 49-57 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C37994 denotes movement
T596 58-66 http://purl.bioontology.org/ontology/SNOMEDCT/64572001 denotes disorder
T597 183-191 http://purl.bioontology.org/ontology/SNOMEDCT/64572001 denotes disorder
T598 218-225 http://purl.bioontology.org/ontology/SNOMEDCT/64572001 denotes disease
T601 58-66 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C2991 denotes disorder
T602 183-191 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C2991 denotes disorder
T603 218-225 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C2991 denotes disease
T606 91-101 http://purl.bioontology.org/ontology/SNOMEDCT/261904005 denotes laboratory
T607 91-101 http://purl.bioontology.org/ontology/MESH/D007753 denotes laboratory
T608 91-101 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C37984 denotes laboratory
T609 116-122 http://purl.bioontology.org/ontology/SNOMEDCT/13039001 denotes series
T611 116-122 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C25674 denotes series
T613 116-122 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C69225 denotes series
T615 141-147 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C142506 denotes define
T616 152-159 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C15238 denotes genetic
T617 152-159 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C17938 denotes genetic
T618 160-166 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C71163 denotes lesion
T619 160-166 http://purl.bioontology.org/ontology/SNOMEDCT/52988006 denotes lesion
T620 160-166 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C3824 denotes lesion
T621 167-177 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C154417 denotes underlying
T622 218-225 http://purl.obolibrary.org/obo/OGMS_0000031 denotes disease
T623 218-225 http://purl.bioontology.org/ontology/NDFRT/N0000000981 denotes disease
T624 218-225 http://purl.bioontology.org/ontology/MESH/D004194 denotes disease