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PMC:1892049 / 0-802 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
T822 0-8 SO_EXT:sequence_deletion_entity_or_process denotes Deletion
T823 12-17 PR_EXT:000009158 denotes ITPR1
T824 38-42 NCBITaxon:10088 denotes Mice
T825 47-62 UBERON:0014643 denotes Spinocerebellar
T826 76-82 NCBITaxon:9606 denotes Humans
T827 143-152 GO:0030849 denotes autosomal
T828 163-171 GO_EXT:biological_movement_or_translocation_process denotes movement
T829 184-188 NCBITaxon:10088 denotes mice
T830 266-273 SO_EXT:0000704 denotes genetic
T831 343-349 NCBITaxon:9606 denotes humans
T832 355-363 SO_EXT:sequence_alteration_entity_or_process denotes mutation
T833 403-411 SO_EXT:biological_sequence denotes sequence
T834 479-487 SO:0001817 denotes in-frame
T835 491-493 SO_EXT:0000028 denotes bp
T836 494-502 SO_EXT:sequence_deletion_entity_or_process denotes deletion
T837 506-511 PR_EXT:000009158 denotes Itpr1
T838 513-518 PR_EXT:000009158 denotes Itpr1
T839 528-536 SO_EXT:sequence_coding_function denotes encoding
T840 537-564 CHEBI_EXT:1D_myo_inositol_1_4_5_trisphosphate denotes inositol 1,4,5-triphosphate
T841 537-573 GO_EXT:0005220 denotes inositol 1,4,5-triphosphate receptor
T842 537-575 PR_EXT:000009158 denotes inositol 1,4,5-triphosphate receptor 1
T843 611-616 PR_EXT:000009158 denotes Itpr1
T844 617-625 SO_EXT:sequence_alteration_entity_or_process denotes mutation
T845 629-633 NCBITaxon:10088 denotes mice
T846 701-709 SO:0001817 denotes in-frame
T847 710-718 SO_EXT:sequence_deletion_entity_or_process denotes deletion
T848 726-731 PR_EXT:000009158 denotes Itpr1
T849 782-787 PR_EXT:000009158 denotes Itpr1
T850 788-798 GO:0010467 denotes expression

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
T788 12-17 PR:000009158 denotes ITPR1
T789 38-42 NCBITaxon:10088 denotes Mice
T790 47-62 UBERON:0014643 denotes Spinocerebellar
T791 76-82 NCBITaxon:9606 denotes Humans
T792 143-152 GO:0030849 denotes autosomal
T793 184-188 NCBITaxon:10088 denotes mice
T794 266-273 SO:0000704 denotes genetic
T795 343-349 NCBITaxon:9606 denotes humans
T796 479-487 SO:0001817 denotes in-frame
T797 491-493 SO:0000028 denotes bp
T798 506-511 PR:000009158 denotes Itpr1
T799 513-518 PR:000009158 denotes Itpr1
T800 537-575 PR:000009158 denotes inositol 1,4,5-triphosphate receptor 1
T801 611-616 PR:000009158 denotes Itpr1
T802 629-633 NCBITaxon:10088 denotes mice
T803 701-709 SO:0001817 denotes in-frame
T804 726-731 PR:000009158 denotes Itpr1
T805 782-787 PR:000009158 denotes Itpr1
T806 788-798 GO:0010467 denotes expression

craft-sa-dev

Id Subject Object Predicate Lexical cue
T871 0-8 NN denotes Deletion
T872 18-27 VBZ denotes Underlies
T873 0-82 sentence denotes Deletion at ITPR1 Underlies Ataxia in Mice and Spinocerebellar Ataxia 15 in Humans
T874 9-11 IN denotes at
T875 12-17 NNP denotes ITPR1
T876 28-34 NN denotes Ataxia
T877 35-37 IN denotes in
T878 38-42 NNS denotes Mice
T879 43-46 CC denotes and
T880 47-62 JJ denotes Spinocerebellar
T881 63-69 NN denotes Ataxia
T882 70-72 CD denotes 15
T883 73-75 IN denotes in
T884 76-82 NNS denotes Humans
T887 82-216 sentence denotes ITPR1 Deletion Causes Ataxia Abstract We observed a severe autosomal recessive movement disorder in mice used within our laboratory.
T888 122-124 PRP denotes We
T889 125-133 VBD denotes observed
T890 134-135 DT denotes a
T891 172-180 NN denotes disorder
T892 136-142 JJ denotes severe
T893 143-152 JJ denotes autosomal
T894 153-162 JJ denotes recessive
T895 163-171 NN denotes movement
T896 181-183 IN denotes in
T897 184-188 NNS denotes mice
T898 189-193 VBN denotes used
T899 194-200 IN denotes within
T900 201-204 PRP$ denotes our
T901 205-215 NN denotes laboratory
T902 215-216 . denotes .
T903 216-382 sentence denotes We pursued a series of experiments to define the genetic lesion underlying this disorder and to identify a cognate disease in humans with mutation at the same locus.
T904 217-219 PRP denotes We
T905 220-227 VBD denotes pursued
T906 228-229 DT denotes a
T907 230-236 NN denotes series
T908 237-239 IN denotes of
T909 240-251 NNS denotes experiments
T910 252-254 TO denotes to
T911 255-261 VB denotes define
T912 262-265 DT denotes the
T913 274-280 NN denotes lesion
T914 266-273 JJ denotes genetic
T915 281-291 VBG denotes underlying
T916 292-296 DT denotes this
T917 297-305 NN denotes disorder
T918 306-309 CC denotes and
T919 310-312 TO denotes to
T920 313-321 VB denotes identify
T921 322-323 DT denotes a
T922 332-339 NN denotes disease
T923 324-331 JJ denotes cognate
T924 340-342 IN denotes in
T925 343-349 NNS denotes humans
T926 350-354 IN denotes with
T927 355-363 NN denotes mutation
T928 364-366 IN denotes at
T929 367-370 DT denotes the
T930 376-381 NN denotes locus
T931 371-375 JJ denotes same
T932 381-382 . denotes .
T933 382-576 sentence denotes Through linkage and sequence analysis we show here that this disorder is caused by a homozygous in-frame 18-bp deletion in Itpr1 (Itpr1Δ18/Δ18), encoding inositol 1,4,5-triphosphate receptor 1.
T934 383-390 IN denotes Through
T935 424-428 VBP denotes show
T936 391-398 NN denotes linkage
T937 412-420 NN denotes analysis
T938 399-402 CC denotes and
T939 403-411 NN denotes sequence
T940 421-423 PRP denotes we
T941 429-433 RB denotes here
T942 434-438 IN denotes that
T943 456-462 VBN denotes caused
T944 439-443 DT denotes this
T945 444-452 NN denotes disorder
T946 453-455 VBZ denotes is
T947 463-465 IN denotes by
T948 466-467 DT denotes a
T949 494-502 NN denotes deletion
T950 468-478 JJ denotes homozygous
T951 479-481 IN denotes in
T952 481-482 HYPH denotes -
T953 482-487 NN denotes frame
T954 488-490 CD denotes 18
T955 491-493 NN denotes bp
T956 490-491 HYPH denotes -
T957 503-505 IN denotes in
T958 506-511 NN denotes Itpr1
T959 512-513 -LRB- denotes (
T960 522-525 NN denotes Δ18
T961 513-518 NN denotes Itpr1
T962 518-521 NN denotes Δ18
T963 521-522 HYPH denotes /
T964 525-526 -RRB- denotes )
T965 526-528 , denotes ,
T966 528-536 VBG denotes encoding
T967 537-545 NN denotes inositol
T968 565-573 NN denotes receptor
T969 546-547 CD denotes 1
T970 550-551 CD denotes 5
T971 547-548 , denotes ,
T972 548-549 CD denotes 4
T973 549-550 , denotes ,
T974 552-564 NN denotes triphosphate
T975 551-552 HYPH denotes -
T976 574-575 CD denotes 1
T977 575-576 . denotes .
T978 576-685 sentence denotes A previously reported spontaneous Itpr1 mutation in mice causes a phenotype identical to that observed here.
T979 577-578 DT denotes A
T980 617-625 NN denotes mutation
T981 579-589 RB denotes previously
T982 590-598 VBN denotes reported
T983 599-610 JJ denotes spontaneous
T984 611-616 NN denotes Itpr1
T985 634-640 VBZ denotes causes
T986 626-628 IN denotes in
T987 629-633 NNS denotes mice
T988 641-642 DT denotes a
T989 643-652 NN denotes phenotype
T990 653-662 JJ denotes identical
T991 663-665 IN denotes to
T992 666-670 DT denotes that
T993 671-679 VBN denotes observed
T994 680-684 RB denotes here
T995 684-685 . denotes .
T997 686-688 IN denotes In
T998 732-737 VBZ denotes leads
T999 689-693 DT denotes both
T1000 694-700 NNS denotes models
T1001 701-703 IN denotes in
T1002 704-709 NN denotes frame
T1003 703-704 HYPH denotes -
T1004 710-718 NN denotes deletion
T1005 719-725 IN denotes within
T1006 726-731 NN denotes Itpr1
T1007 738-740 IN denotes to
T1008 741-742 DT denotes a
T1009 743-751 NN denotes decrease
T1010 752-754 IN denotes in
T1011 755-758 DT denotes the
T1012 773-778 NN denotes level
T1013 759-767 RB denotes normally
T1014 768-772 JJ denotes high
T1015 779-781 IN denotes of
T1016 782-787 NN denotes Itpr1
T1017 788-798 NN denotes expression
T1018 799-801 IN denotes in
R66 T944 T945 det this,disorder
R3 T871 T872 nsubj Deletion,Underlies
R4 T874 T871 prep at,Deletion
R5 T875 T874 pobj ITPR1,at
R6 T876 T872 dobj Ataxia,Underlies
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
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
R49 T925 T924 pobj humans,in
R50 T926 T925 prep with,humans
R51 T927 T926 pobj mutation,with
R52 T928 T927 prep at,mutation
R53 T929 T930 det the,locus
R54 T930 T928 pobj locus,at
R55 T931 T930 amod same,locus
R56 T932 T905 punct .,pursued
R57 T934 T935 prep Through,show
R58 T936 T937 nmod linkage,analysis
R60 T938 T936 cc and,linkage
R61 T939 T936 conj sequence,linkage
R62 T940 T935 nsubj we,show
R63 T941 T935 advmod here,show
R64 T942 T943 mark that,caused
R65 T943 T935 ccomp caused,show
R67 T945 T943 nsubjpass disorder,caused
R68 T946 T943 auxpass is,caused
R69 T947 T943 agent by,caused
R70 T948 T949 det a,deletion
R71 T949 T947 pobj deletion,by
R72 T950 T949 amod homozygous,deletion
R73 T951 T949 nmod in,deletion
R74 T952 T951 punct -,in
R75 T953 T951 pobj frame,in
R76 T954 T955 nummod 18,bp
R77 T955 T949 compound bp,deletion
R78 T956 T955 punct -,bp
R79 T957 T949 prep in,deletion
R80 T958 T957 pobj Itpr1,in
R81 T959 T960 punct (,Δ18
R82 T960 T958 parataxis Δ18,Itpr1
R83 T961 T960 compound Itpr1,Δ18
R84 T962 T960 compound Δ18,Δ18
R85 T963 T960 punct /,Δ18
R86 T964 T960 punct ),Δ18
R87 T965 T949 punct ", ",deletion
R88 T966 T949 acl encoding,deletion
R89 T967 T968 nmod inositol,receptor
R90 T968 T966 dobj receptor,encoding
R91 T969 T970 nummod 1,5
R93 T971 T970 punct ",",5
R94 T972 T970 nummod 4,5
R95 T973 T970 punct ",",5
R96 T974 T968 compound triphosphate,receptor
R97 T975 T974 punct -,triphosphate
R98 T976 T968 nummod 1,receptor
R99 T977 T935 punct .,show
R100 T979 T980 det A,mutation
R101 T980 T985 nsubj mutation,causes
R102 T981 T982 advmod previously,reported
R103 T982 T980 amod reported,mutation
R104 T983 T980 amod spontaneous,mutation
R105 T984 T980 compound Itpr1,mutation
R106 T986 T980 prep in,mutation
R107 T987 T986 pobj mice,in
R108 T988 T989 det a,phenotype
R109 T989 T985 dobj phenotype,causes
R110 T990 T989 amod identical,phenotype
R111 T991 T990 prep to,identical
R112 T992 T991 pobj that,to
R113 T993 T992 acl observed,that
R114 T994 T993 advmod here,observed
R115 T995 T985 punct .,causes
R116 T997 T998 prep In,leads
R117 T999 T1000 det both,models
R118 T1000 T997 pobj models,In
R119 T1001 T1002 nmod in,frame
R120 T1002 T1004 compound frame,deletion
R121 T1003 T1002 punct -,frame
R122 T1004 T998 nsubj deletion,leads
R123 T1005 T1004 prep within,deletion
R124 T1006 T1005 pobj Itpr1,within
R125 T1007 T998 prep to,leads
R126 T1008 T1009 det a,decrease
R127 T1009 T1007 pobj decrease,to
R128 T1010 T1009 prep in,decrease
R129 T1011 T1012 det the,level
R131 T1013 T1014 advmod normally,high
R132 T1014 T1012 amod high,level
R133 T1015 T1012 prep of,level
R134 T1016 T1017 compound Itpr1,expression
R135 T1017 T1015 pobj expression,of
R136 T1018 T1017 prep in,expression
R59 T937 T934 pobj analysis,Through
R92 T970 T974 nummod 5,triphosphate
R130 T1012 T1010 pobj level,in

Biotea

Id Subject Object Predicate Lexical cue
T510 63-69 http://purl.bioontology.org/ontology/OMIM/MTHU036349 denotes Ataxia
T513 28-34 http://purl.obolibrary.org/obo/SYMP_0000005 denotes Ataxia
T514 63-69 http://purl.obolibrary.org/obo/SYMP_0000005 denotes Ataxia
T517 28-34 http://purl.bioontology.org/ontology/MEDDRA/10003591 denotes Ataxia
T518 63-69 http://purl.bioontology.org/ontology/MEDDRA/10003591 denotes Ataxia
T521 28-34 http://purl.bioontology.org/ontology/MEDLINEPLUS/C0004134 denotes Ataxia
T522 63-69 http://purl.bioontology.org/ontology/MEDLINEPLUS/C0004134 denotes Ataxia
T525 28-34 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C26702 denotes Ataxia
T526 63-69 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C26702 denotes Ataxia
T529 28-34 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C146737 denotes Ataxia
T530 63-69 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C146737 denotes Ataxia
T533 28-34 http://purl.bioontology.org/ontology/SNOMEDCT/20262006 denotes Ataxia
T534 63-69 http://purl.bioontology.org/ontology/SNOMEDCT/20262006 denotes Ataxia
T537 28-34 http://purl.bioontology.org/ontology/MESH/D001259 denotes Ataxia
T538 63-69 http://purl.bioontology.org/ontology/MESH/D001259 denotes Ataxia
T541 38-42 http://purl.obolibrary.org/obo/PR_O89094 denotes Mice
T542 184-188 http://purl.obolibrary.org/obo/PR_O89094 denotes mice
T543 629-633 http://purl.obolibrary.org/obo/PR_O89094 denotes mice
T545 38-42 http://purl.obolibrary.org/obo/PR_000005054 denotes Mice
T546 184-188 http://purl.obolibrary.org/obo/PR_000005054 denotes mice
T547 629-633 http://purl.obolibrary.org/obo/PR_000005054 denotes mice
T549 38-42 http://purl.bioontology.org/ontology/MESH/D051379 denotes Mice
T550 184-188 http://purl.bioontology.org/ontology/MESH/D051379 denotes mice
T551 629-633 http://purl.bioontology.org/ontology/MESH/D051379 denotes mice
T553 38-42 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C14238 denotes Mice
T554 184-188 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C14238 denotes mice
T555 629-633 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C14238 denotes mice
T557 47-72 http://purl.bioontology.org/ontology/MESH/C564685 denotes Spinocerebellar Ataxia 15
T559 47-72 http://purl.bioontology.org/ontology/OMIM/606658 denotes Spinocerebellar Ataxia 15
T564 47-69 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C82341 denotes Spinocerebellar Ataxia
T566 47-69 http://purl.bioontology.org/ontology/MEDDRA/10057660 denotes Spinocerebellar Ataxia
T568 47-69 http://purl.bioontology.org/ontology/OMIM/MTHU004242 denotes Spinocerebellar Ataxia
T570 47-69 http://purl.bioontology.org/ontology/SNOMEDCT/129609000 denotes Spinocerebellar Ataxia
T572 76-82 http://purl.bioontology.org/ontology/MESH/D006801 denotes Humans
T573 343-349 http://purl.bioontology.org/ontology/MESH/D006801 denotes humans
T575 125-133 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C25599 denotes observed
T576 671-679 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C25599 denotes observed
T577 136-142 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C121395 denotes severe
T578 136-142 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C122951 denotes severe
T579 136-142 http://purl.bioontology.org/ontology/SNOMEDCT/24484000 denotes severe
T580 136-142 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C41340 denotes severe
T581 136-142 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C156244 denotes severe
T582 136-142 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C70667 denotes severe
T583 143-162 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C94246 denotes autosomal recessive
T584 143-162 http://purl.bioontology.org/ontology/SNOMEDCT/258211005 denotes autosomal recessive
T585 143-162 http://purl.bioontology.org/ontology/OMIM/MTHU000016 denotes autosomal recessive
T586 143-152 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C32168 denotes autosomal
T588 163-180 http://purl.bioontology.org/ontology/OMIM/MTHU044333 denotes movement disorder
T589 163-180 http://purl.bioontology.org/ontology/MEDDRA/10028035 denotes movement disorder
T590 163-180 http://purl.bioontology.org/ontology/SNOMEDCT/60342002 denotes movement disorder
T591 163-180 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C116757 denotes movement disorder
T592 163-171 http://purl.bioontology.org/ontology/MESH/D009068 denotes movement
T593 163-171 http://purl.bioontology.org/ontology/OMIM/MTHU000756 denotes movement
T594 163-171 http://purl.bioontology.org/ontology/SNOMEDCT/255324009 denotes movement
T595 163-171 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C37994 denotes movement
T596 172-180 http://purl.bioontology.org/ontology/SNOMEDCT/64572001 denotes disorder
T597 297-305 http://purl.bioontology.org/ontology/SNOMEDCT/64572001 denotes disorder
T598 332-339 http://purl.bioontology.org/ontology/SNOMEDCT/64572001 denotes disease
T599 444-452 http://purl.bioontology.org/ontology/SNOMEDCT/64572001 denotes disorder
T601 172-180 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C2991 denotes disorder
T602 297-305 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C2991 denotes disorder
T603 332-339 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C2991 denotes disease
T604 444-452 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C2991 denotes disorder
T606 205-215 http://purl.bioontology.org/ontology/SNOMEDCT/261904005 denotes laboratory
T607 205-215 http://purl.bioontology.org/ontology/MESH/D007753 denotes laboratory
T608 205-215 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C37984 denotes laboratory
T609 230-236 http://purl.bioontology.org/ontology/SNOMEDCT/13039001 denotes series
T611 230-236 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C25674 denotes series
T613 230-236 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C69225 denotes series
T615 255-261 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C142506 denotes define
T616 266-273 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C15238 denotes genetic
T617 266-273 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C17938 denotes genetic
T618 274-280 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C71163 denotes lesion
T619 274-280 http://purl.bioontology.org/ontology/SNOMEDCT/52988006 denotes lesion
T620 274-280 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C3824 denotes lesion
T621 281-291 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C154417 denotes underlying
T622 332-339 http://purl.obolibrary.org/obo/OGMS_0000031 denotes disease
T623 332-339 http://purl.bioontology.org/ontology/NDFRT/N0000000981 denotes disease
T624 332-339 http://purl.bioontology.org/ontology/MESH/D004194 denotes disease
T625 355-363 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C16885 denotes mutation
T626 617-625 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C16885 denotes mutation
T628 355-363 http://purl.bioontology.org/ontology/MESH/D009154 denotes mutation
T629 617-625 http://purl.bioontology.org/ontology/MESH/D009154 denotes mutation
T632 355-363 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C45576 denotes mutation
T633 617-625 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C45576 denotes mutation
T635 376-381 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C45822 denotes locus
T636 391-398 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C94542 denotes linkage
T637 403-420 http://purl.bioontology.org/ontology/MESH/D017421 denotes sequence analysis
T638 403-420 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C17565 denotes sequence analysis
T639 403-411 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C43465 denotes sequence
T640 403-411 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C89252 denotes sequence
T641 403-411 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C13299 denotes sequence
T642 403-411 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C25673 denotes sequence
T643 403-411 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C45374 denotes sequence
T644 403-411 http://purl.obolibrary.org/obo/SO_0000001 denotes sequence
T646 412-420 http://purl.bioontology.org/ontology/MESH/Q000032 denotes analysis
T647 412-420 http://purl.bioontology.org/ontology/SNOMEDCT/272389005 denotes analysis
T648 412-420 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C25391 denotes analysis
T649 468-478 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C45826 denotes homozygous
T650 482-487 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C49963 denotes frame
T651 704-709 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C49963 denotes frame
T652 482-487 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C63552 denotes frame
T653 704-709 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C63552 denotes frame
T654 482-487 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C80261 denotes frame
T655 704-709 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C80261 denotes frame
T656 482-487 http://purl.bioontology.org/ontology/SNOMEDCT/257297007 denotes frame
T657 704-709 http://purl.bioontology.org/ontology/SNOMEDCT/257297007 denotes frame
T658 506-511 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C51556 denotes Itpr1
T659 611-616 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C51556 denotes Itpr1
T660 726-731 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C51556 denotes Itpr1
T661 782-787 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C51556 denotes Itpr1
T669 506-511 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C24527 denotes Itpr1
T670 611-616 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C24527 denotes Itpr1
T671 726-731 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C24527 denotes Itpr1
T672 782-787 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C24527 denotes Itpr1
T678 506-511 http://purl.obolibrary.org/obo/PR_000009158 denotes Itpr1
T679 611-616 http://purl.obolibrary.org/obo/PR_000009158 denotes Itpr1
T680 726-731 http://purl.obolibrary.org/obo/PR_000009158 denotes Itpr1
T681 782-787 http://purl.obolibrary.org/obo/PR_000009158 denotes Itpr1
T686 528-536 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C80216 denotes encoding
T687 537-564 http://purl.bioontology.org/ontology/MESH/D015544 denotes inositol 1,4,5-triphosphate
T688 537-564 http://purl.bioontology.org/ontology/NDFRT/N0000168540 denotes inositol 1,4,5-triphosphate
T689 537-545 http://purl.bioontology.org/ontology/NDFRT/N0000146062 denotes inositol
T690 537-545 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C28163 denotes inositol
T691 537-545 http://purl.bioontology.org/ontology/NDDF/002057 denotes inositol
T692 537-545 http://purl.bioontology.org/ontology/NDFRT/N0000007204 denotes inositol
T693 537-545 http://purl.bioontology.org/ontology/MESH/D007294 denotes inositol
T694 537-545 http://purl.bioontology.org/ontology/SNOMEDCT/72164009 denotes inositol
T695 565-573 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C18106 denotes receptor
T696 565-573 http://purl.bioontology.org/ontology/STY/T192 denotes receptor
T697 565-573 http://purl.bioontology.org/ontology/STY/T192 denotes receptor
T698 565-573 http://purl.bioontology.org/ontology/STY/T192 denotes receptor
T699 565-573 http://purl.bioontology.org/ontology/STY/T192 denotes receptor
T700 565-573 http://purl.bioontology.org/ontology/STY/T192 denotes receptor
T701 565-573 http://purl.bioontology.org/ontology/STY/T192 denotes receptor
T702 565-573 http://purl.bioontology.org/ontology/STY/T192 denotes receptor
T703 565-573 http://purl.bioontology.org/ontology/STY/T192 denotes receptor
T704 565-573 http://purl.bioontology.org/ontology/STY/T192 denotes receptor
T705 565-573 http://purl.bioontology.org/ontology/SNOMEDCT/116647005 denotes receptor
T706 590-598 http://purl.bioontology.org/ontology/SNOMEDCT/733985002 denotes reported
T707 590-598 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C25375 denotes reported
T708 599-610 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C48307 denotes spontaneous
T709 599-610 http://purl.bioontology.org/ontology/SNOMEDCT/5054005 denotes spontaneous
T710 643-652 http://purl.obolibrary.org/obo/OGMS_0000023 denotes phenotype
T711 643-652 http://purl.bioontology.org/ontology/SNOMEDCT/8116006 denotes phenotype
T712 643-652 http://purl.bioontology.org/ontology/MESH/D010641 denotes phenotype
T713 643-652 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C16977 denotes phenotype
T714 653-662 http://purl.bioontology.org/ontology/SNOMEDCT/20323000 denotes identical
T715 653-662 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C49034 denotes identical
T716 694-700 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C16866 denotes models
T717 743-751 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C25640 denotes decrease
T718 743-751 http://purl.bioontology.org/ontology/SNOMEDCT/260370003 denotes decrease
T719 768-778 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C129474 denotes high level
T720 773-778 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C87192 denotes level
T721 773-778 http://purl.bioontology.org/ontology/SNOMEDCT/276625007 denotes level
T722 773-778 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C25554 denotes level
T723 788-798 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C80488 denotes expression
T724 788-798 http://purl.bioontology.org/ontology/SNOMEDCT/706999006 denotes expression
T725 788-798 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C16608 denotes expression
T726 788-798 http://purl.bioontology.org/ontology/SNOMEDCT/10012005 denotes expression
T489 0-8 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C61330 denotes Deletion
T490 494-502 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C61330 denotes deletion
T491 710-718 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C61330 denotes deletion
T493 0-8 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C19296 denotes Deletion
T494 494-502 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C19296 denotes deletion
T495 710-718 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C19296 denotes deletion
T497 0-8 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C45583 denotes Deletion
T498 494-502 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C45583 denotes deletion
T499 710-718 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C45583 denotes deletion
T501 0-8 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C45577 denotes Deletion
T502 494-502 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C45577 denotes deletion
T503 710-718 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C45577 denotes deletion
T505 0-8 http://purl.bioontology.org/ontology/SNOMEDCT/737543005 denotes Deletion
T506 494-502 http://purl.bioontology.org/ontology/SNOMEDCT/737543005 denotes deletion
T507 710-718 http://purl.bioontology.org/ontology/SNOMEDCT/737543005 denotes deletion
T509 28-34 http://purl.bioontology.org/ontology/OMIM/MTHU036349 denotes Ataxia