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PMC:1892049 / 16407-17803 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
T6278 0-5 PR_EXT:000009158 denotes Itpr1
T6279 21-28 SO_EXT:0000417 denotes domains
T6280 33-43 CHEBI_SO_EXT:N_terminus_or_N_terminal_region denotes N-terminal
T6281 44-65 CHEBI:25450 denotes inositol triphosphate
T6282 66-73 CHEMINF_GO_EXT:chemical_binding_or_bond_formation denotes binding
T6283 66-80 SO_EXT:0100018 denotes binding domain
T6284 93-99 SO_EXT:0000417 denotes domain
T6285 107-117 CHEBI_SO_EXT:C_terminus_or_C_terminal_region denotes C-terminal
T6286 123-131 GO:0016020 denotes membrane
T6287 161-168 CHEBI_PR_EXT:protein denotes protein
T6288 161-177 GO_EXT:0004691 denotes protein kinase A
T6289 178-193 GO_PATO_EXT:phosphorylation_process denotes phosphorylation
T6290 207-210 CHEBI_EXT:ATP denotes ATP
T6291 211-218 CHEMINF_GO_EXT:chemical_binding_or_bond_formation denotes binding
T6292 211-223 SO_EXT:0000409 denotes binding site
T6293 225-230 PR_EXT:000009158 denotes Itpr1
T6294 245-249 CHEBI:29108 denotes Ca2+
T6295 245-258 GO_EXT:0005262 denotes Ca2+ channels
T6296 275-279 CHEBI:29108 denotes Ca2+
T6297 280-287 GO_EXT:biological_release denotes release
T6298 297-318 GO:0005783 denotes endoplasmic reticulum
T6299 325-332 CHEMINF_GO_EXT:chemical_binding_or_bond_formation denotes binding
T6300 340-353 GO:0005622 denotes intracellular
T6301 345-353 CL_GO_EXT:cell denotes cellular
T6302 361-370 CHEBI_EXT:33280 denotes messenger
T6303 371-398 CHEBI_EXT:1D_myo_inositol_1_4_5_trisphosphate denotes inositol 1,4,5-triphosphate
T6304 404-409 PR_EXT:000009158 denotes Itpr1
T6305 429-446 _FRAGMENT denotes Purkinje cells of
T6306 451-461 CL:0000121 denotes cerebellum
T6307 438-443 CL_GO_EXT:cell denotes cells
T6308 451-461 UBERON:0002037 denotes cerebellum
T6309 467-472 PR_EXT:000009158 denotes ITPR1
T6310 473-482 SO_EXT:sequence_alteration_entity_or_process denotes mutations
T6311 594-599 PR_EXT:000009158 denotes ITPR1
T6312 667-675 SO_EXT:sequence_deletion_entity_or_process denotes deletion
T6313 711-717 NCBITaxon:9606 denotes humans
T6314 738-746 SO_EXT:sequence_deletion_entity_or_process denotes deletion
T6315 750-754 NCBITaxon:10088 denotes mice
T6316 834-843 UBERON:0000104 denotes life span
T6317 851-856 NCBITaxon:10088 denotes mouse
T6318 915-925 SO_EXT:0000318 denotes start site
T6319 930-935 PR_EXT:000009158 denotes ITPR1
T6320 1015-1022 CHEBI_PR_EXT:protein denotes protein
T6321 1058-1063 CL_GO_EXT:cell denotes cells
T6322 1136-1144 GO:0042571 denotes antibody
T6323 1164-1174 CHEBI_SO_EXT:C_terminus_or_C_terminal_region denotes C-terminal
T6324 1186-1191 PR_EXT:000009158 denotes ITPR1
T6325 1233-1242 SO_EXT:sequence_truncation_process denotes truncated
T6326 1243-1250 CHEBI_PR_EXT:protein denotes protein
T6327 1301-1306 PR_EXT:000009158 denotes ITPR1
T6328 1307-1316 SO_EXT:sequence_alteration_entity_or_process denotes mutations
R405 T6306 T6305 _lexicallyChainedTo cerebellum,Purkinje cells of

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
T5964 0-5 PR:000009158 denotes Itpr1
T5965 21-28 SO:0000417 denotes domains
T5966 44-65 CHEBI:25450 denotes inositol triphosphate
T5967 66-80 SO:0100018 denotes binding domain
T5968 93-99 SO:0000417 denotes domain
T5969 123-131 GO:0016020 denotes membrane
T5970 211-223 SO:0000409 denotes binding site
T5971 225-230 PR:000009158 denotes Itpr1
T5972 245-249 CHEBI:29108 denotes Ca2+
T5973 275-279 CHEBI:29108 denotes Ca2+
T5974 297-318 GO:0005783 denotes endoplasmic reticulum
T5975 340-353 GO:0005622 denotes intracellular
T5976 361-370 CHEBI:33280 denotes messenger
T5977 404-409 PR:000009158 denotes Itpr1
T5978 429-446 _FRAGMENT denotes Purkinje cells of
T5979 451-461 CL:0000121 denotes cerebellum
T5980 451-461 UBERON:0002037 denotes cerebellum
T5981 467-472 PR:000009158 denotes ITPR1
T5982 594-599 PR:000009158 denotes ITPR1
T5983 711-717 NCBITaxon:9606 denotes humans
T5984 750-754 NCBITaxon:10088 denotes mice
T5985 834-843 UBERON:0000104 denotes life span
T5986 851-856 NCBITaxon:10088 denotes mouse
T5987 915-925 SO:0000318 denotes start site
T5988 930-935 PR:000009158 denotes ITPR1
T5989 1136-1144 GO:0042571 denotes antibody
T5990 1186-1191 PR:000009158 denotes ITPR1
T5991 1301-1306 PR:000009158 denotes ITPR1
R401 T5979 T5978 _lexicallyChainedTo cerebellum,Purkinje cells of

craft-sa-dev

Id Subject Object Predicate Lexical cue
T8123 0-5 NN denotes Itpr1
T8124 6-14 VBZ denotes contains
T8125 148-156 VBZ denotes contains
T8126 15-20 CD denotes three
T8127 21-28 NNS denotes domains
T8128 28-30 , denotes ,
T8129 30-32 DT denotes an
T8130 74-80 NN denotes domain
T8131 33-34 NN denotes N
T8132 35-43 JJ denotes terminal
T8133 34-35 HYPH denotes -
T8134 44-52 NN denotes inositol
T8135 53-65 NN denotes triphosphate
T8136 66-73 NN denotes binding
T8137 80-82 , denotes ,
T8138 82-83 DT denotes a
T8139 93-99 NN denotes domain
T8140 84-92 VBG denotes coupling
T8141 99-101 , denotes ,
T8142 101-104 CC denotes and
T8143 105-106 DT denotes a
T8144 132-138 NN denotes domain
T8145 107-108 NN denotes C
T8146 109-117 JJ denotes terminal
T8147 108-109 HYPH denotes -
T8148 118-131 NN denotes transmembrane
T8149 138-139 : denotes ;
T8150 140-142 PRP denotes it
T8151 143-147 RB denotes also
T8152 157-160 CD denotes two
T8153 194-199 NNS denotes sites
T8154 161-168 NN denotes protein
T8155 176-177 NN denotes A
T8156 169-175 NN denotes kinase
T8157 178-193 NN denotes phosphorylation
T8158 200-203 CC denotes and
T8159 204-206 DT denotes an
T8160 219-223 NN denotes site
T8161 207-210 NN denotes ATP
T8162 211-218 VBG denotes binding
T8163 210-211 HYPH denotes -
T8164 223-224 . denotes .
T8165 224-403 sentence denotes Itpr1 is coupled to Ca2+ channels and facilitates Ca2+ release from the endoplasmic reticulum after binding by the intracellular second messenger inositol 1,4,5-triphosphate [9].
T8166 225-230 NN denotes Itpr1
T8167 234-241 VBN denotes coupled
T8168 231-233 VBZ denotes is
T8169 242-244 IN denotes to
T8170 245-249 NN denotes Ca2+
T8171 250-258 NNS denotes channels
T8172 259-262 CC denotes and
T8173 263-274 VBZ denotes facilitates
T8174 275-279 NN denotes Ca2+
T8175 280-287 NN denotes release
T8176 288-292 IN denotes from
T8177 293-296 DT denotes the
T8178 309-318 NN denotes reticulum
T8179 297-308 JJ denotes endoplasmic
T8180 319-324 IN denotes after
T8181 325-332 NN denotes binding
T8182 333-335 IN denotes by
T8183 336-339 DT denotes the
T8184 361-370 NN denotes messenger
T8185 340-353 JJ denotes intracellular
T8186 354-360 JJ denotes second
T8187 371-379 NN denotes inositol
T8188 386-398 NN denotes triphosphate
T8189 380-381 CD denotes 1
T8190 384-385 CD denotes 5
T8191 381-382 , denotes ,
T8192 382-383 CD denotes 4
T8193 383-384 , denotes ,
T8194 385-386 HYPH denotes -
T8195 399-400 -LRB- denotes [
T8196 400-401 CD denotes 9
T8197 401-402 -RRB- denotes ]
T8198 402-403 . denotes .
T8199 403-466 sentence denotes Itpr1 is enriched in the Purkinje cells of the cerebellum [4].
T8200 404-409 NN denotes Itpr1
T8201 413-421 VBN denotes enriched
T8202 410-412 VBZ denotes is
T8203 422-424 IN denotes in
T8204 425-428 DT denotes the
T8205 438-443 NNS denotes cells
T8206 429-437 NNP denotes Purkinje
T8207 444-446 IN denotes of
T8208 447-450 DT denotes the
T8209 451-461 NN denotes cerebellum
T8210 462-463 -LRB- denotes [
T8211 463-464 CD denotes 4
T8212 464-465 -RRB- denotes ]
T8213 465-466 . denotes .
T8214 466-533 sentence denotes ITPR1 mutations have more than one potential pathogenic mechanism.
T8215 467-472 NN denotes ITPR1
T8216 473-482 NNS denotes mutations
T8217 483-487 VBP denotes have
T8218 488-492 JJR denotes more
T8219 498-501 CD denotes one
T8220 493-497 IN denotes than
T8221 523-532 NN denotes mechanism
T8222 502-511 JJ denotes potential
T8223 512-522 JJ denotes pathogenic
T8224 532-533 . denotes .
T8225 533-857 sentence denotes First, the disease may be a result of haploinsufficiency at ITPR1; this concept is consistent with the observation that heterozygous deletion leads to a later onset disorder in humans, whereas homozygous deletion in mice leads to an early onset disorder, able to be expressed within the much shorter life span of the mouse.
T8226 534-539 RB denotes First
T8227 614-616 VBZ denotes is
T8228 539-541 , denotes ,
T8229 541-544 DT denotes the
T8230 545-552 NN denotes disease
T8231 557-559 VB denotes be
T8232 553-556 MD denotes may
T8233 560-561 DT denotes a
T8234 562-568 NN denotes result
T8235 569-571 IN denotes of
T8236 572-590 NN denotes haploinsufficiency
T8237 591-593 IN denotes at
T8238 594-599 NN denotes ITPR1
T8239 599-600 : denotes ;
T8240 601-605 DT denotes this
T8241 606-613 NN denotes concept
T8242 617-627 JJ denotes consistent
T8243 628-632 IN denotes with
T8244 633-636 DT denotes the
T8245 637-648 NN denotes observation
T8246 649-653 IN denotes that
T8247 676-681 VBZ denotes leads
T8248 654-666 JJ denotes heterozygous
T8249 667-675 NN denotes deletion
T8250 682-684 IN denotes to
T8251 685-686 DT denotes a
T8252 699-707 NN denotes disorder
T8253 687-692 JJ denotes later
T8254 693-698 NN denotes onset
T8255 708-710 IN denotes in
T8256 711-717 NNS denotes humans
T8257 717-719 , denotes ,
T8258 719-726 IN denotes whereas
T8259 755-760 VBZ denotes leads
T8260 727-737 JJ denotes homozygous
T8261 738-746 NN denotes deletion
T8262 747-749 IN denotes in
T8263 750-754 NNS denotes mice
T8264 761-763 IN denotes to
T8265 764-766 DT denotes an
T8266 779-787 NN denotes disorder
T8267 767-772 JJ denotes early
T8268 773-778 NN denotes onset
T8269 787-789 , denotes ,
T8270 789-793 JJ denotes able
T8271 794-796 TO denotes to
T8272 800-809 VBN denotes expressed
T8273 797-799 VB denotes be
T8274 810-816 IN denotes within
T8275 817-820 DT denotes the
T8276 839-843 NN denotes span
T8277 821-825 RB denotes much
T8278 826-833 JJR denotes shorter
T8279 834-838 NN denotes life
T8280 844-846 IN denotes of
T8281 847-850 DT denotes the
T8282 851-856 NN denotes mouse
T8283 856-857 . denotes .
T8284 857-1260 sentence denotes Second, we cannot rule out the existence of an alternate start site for ITPR1 that may result in a product that confers a pathogenic gain of function to the protein; however, Western blot analysis of cells derived from affected AUS1 family members, which was performed using an antibody raised against the C-terminal portion of ITPR1, failed to identify any disease-specific truncated protein products.
T8285 858-864 RB denotes Second
T8286 1193-1199 VBD denotes failed
T8287 864-866 , denotes ,
T8288 866-868 PRP denotes we
T8289 876-880 VB denotes rule
T8290 869-872 MD denotes can
T8291 872-875 RB denotes not
T8292 881-884 RP denotes out
T8293 885-888 DT denotes the
T8294 889-898 NN denotes existence
T8295 899-901 IN denotes of
T8296 902-904 DT denotes an
T8297 921-925 NN denotes site
T8298 905-914 JJ denotes alternate
T8299 915-920 NN denotes start
T8300 926-929 IN denotes for
T8301 930-935 NN denotes ITPR1
T8302 936-940 WDT denotes that
T8303 945-951 VB denotes result
T8304 941-944 MD denotes may
T8305 952-954 IN denotes in
T8306 955-956 DT denotes a
T8307 957-964 NN denotes product
T8308 965-969 WDT denotes that
T8309 970-977 VBZ denotes confers
T8310 978-979 DT denotes a
T8311 991-995 NN denotes gain
T8312 980-990 JJ denotes pathogenic
T8313 996-998 IN denotes of
T8314 999-1007 NN denotes function
T8315 1008-1010 IN denotes to
T8316 1011-1014 DT denotes the
T8317 1015-1022 NN denotes protein
T8318 1022-1023 : denotes ;
T8319 1024-1031 RB denotes however
T8320 1031-1033 , denotes ,
T8321 1033-1040 NNP denotes Western
T8322 1041-1045 NN denotes blot
T8323 1046-1054 NN denotes analysis
T8324 1055-1057 IN denotes of
T8325 1058-1063 NNS denotes cells
T8326 1064-1071 VBN denotes derived
T8327 1072-1076 IN denotes from
T8328 1077-1085 VBN denotes affected
T8329 1098-1105 NNS denotes members
T8330 1086-1090 NN denotes AUS1
T8331 1091-1097 NN denotes family
T8332 1105-1107 , denotes ,
T8333 1107-1112 WDT denotes which
T8334 1117-1126 VBN denotes performed
T8335 1113-1116 VBD denotes was
T8336 1127-1132 VBG denotes using
T8337 1133-1135 DT denotes an
T8338 1136-1144 NN denotes antibody
T8339 1145-1151 VBN denotes raised
T8340 1152-1159 IN denotes against
T8341 1160-1163 DT denotes the
T8342 1175-1182 NN denotes portion
T8343 1164-1165 NN denotes C
T8344 1166-1174 JJ denotes terminal
T8345 1165-1166 HYPH denotes -
T8346 1183-1185 IN denotes of
T8347 1186-1191 NN denotes ITPR1
T8348 1191-1193 , denotes ,
T8349 1200-1202 TO denotes to
T8350 1203-1211 VB denotes identify
T8351 1212-1215 DT denotes any
T8352 1251-1259 NNS denotes products
T8353 1216-1223 NN denotes disease
T8354 1224-1232 JJ denotes specific
T8355 1223-1224 HYPH denotes -
T8356 1233-1242 VBN denotes truncated
T8357 1243-1250 NN denotes protein
T8358 1259-1260 . denotes .
T8359 1260-1396 sentence denotes Clearly, the identification of distinct ITPR1 mutations underlying SCA15 will help elucidate the pathogenic mechanism of this disorder.
T8360 1261-1268 RB denotes Clearly
T8361 1339-1343 VB denotes help
T8362 1268-1270 , denotes ,
T8363 1270-1273 DT denotes the
T8364 1274-1288 NN denotes identification
T8365 1289-1291 IN denotes of
T8366 1292-1300 JJ denotes distinct
T8367 1307-1316 NNS denotes mutations
T8368 1301-1306 NN denotes ITPR1
T8369 1317-1327 VBG denotes underlying
T8370 1328-1333 NN denotes SCA15
T8371 1334-1338 MD denotes will
T8372 1344-1353 VB denotes elucidate
T8373 1354-1357 DT denotes the
T8374 1369-1378 NN denotes mechanism
T8375 1358-1368 JJ denotes pathogenic
T8376 1379-1381 IN denotes of
T8377 1382-1386 DT denotes this
T8378 1387-1395 NN denotes disorder
T8379 1395-1396 . denotes .
R2029 T8123 T8124 nsubj Itpr1,contains
R2030 T8124 T8125 ccomp contains,contains
R2032 T8126 T8127 nummod three,domains
R2033 T8127 T8124 dobj domains,contains
R2035 T8128 T8127 punct ", ",domains
R2037 T8129 T8130 det an,domain
R2039 T8130 T8127 appos domain,domains
R2040 T8131 T8132 npadvmod N,terminal
R2041 T8132 T8130 amod terminal,domain
R2043 T8133 T8132 punct -,terminal
R2044 T8134 T8130 compound inositol,domain
R2045 T8135 T8130 compound triphosphate,domain
R2047 T8136 T8130 compound binding,domain
R2048 T8137 T8130 punct ", ",domain
R2050 T8138 T8139 det a,domain
R2051 T8139 T8130 conj domain,domain
R2052 T8140 T8139 amod coupling,domain
R2054 T8141 T8139 punct ", ",domain
R2055 T8142 T8139 cc and,domain
R2057 T8143 T8144 det a,domain
R2058 T8144 T8139 conj domain,domain
R2059 T8145 T8146 npadvmod C,terminal
R2061 T8146 T8144 amod terminal,domain
R2062 T8147 T8146 punct -,terminal
R2063 T8148 T8144 compound transmembrane,domain
R2064 T8149 T8125 punct ;,contains
R2065 T8150 T8125 nsubj it,contains
R2067 T8151 T8125 advmod also,contains
R2068 T8152 T8153 nummod two,sites
R2069 T8153 T8125 dobj sites,contains
R2071 T8154 T8155 compound protein,A
R2072 T8155 T8153 compound A,sites
R2073 T8156 T8155 compound kinase,A
R2075 T8157 T8153 compound phosphorylation,sites
R2076 T8158 T8153 cc and,sites
R2077 T8159 T8160 det an,site
R2079 T8160 T8153 conj site,sites
R2080 T8161 T8162 npadvmod ATP,binding
R2081 T8162 T8160 amod binding,site
R2083 T8163 T8162 punct -,binding
R2084 T8164 T8125 punct .,contains
R2086 T8166 T8167 nsubjpass Itpr1,coupled
R2088 T8168 T8167 auxpass is,coupled
R2089 T8169 T8167 prep to,coupled
R2091 T8170 T8171 compound Ca2+,channels
R2094 T8171 T8169 pobj channels,to
R2095 T8172 T8167 cc and,coupled
R2097 T8173 T8167 conj facilitates,coupled
R2098 T8174 T8175 compound Ca2+,release
R2099 T8175 T8173 dobj release,facilitates
R2100 T8176 T8175 prep from,release
R2102 T8177 T8178 det the,reticulum
R2103 T8178 T8176 pobj reticulum,from
R2105 T8179 T8178 amod endoplasmic,reticulum
R2106 T8180 T8175 prep after,release
R2107 T8181 T8180 pobj binding,after
R2109 T8182 T8181 prep by,binding
R2110 T8183 T8184 det the,messenger
R2111 T8184 T8182 pobj messenger,by
R2113 T8185 T8184 amod intracellular,messenger
R2114 T8186 T8184 amod second,messenger
R2115 T8187 T8188 nmod inositol,triphosphate
R2116 T8188 T8184 appos triphosphate,messenger
R2117 T8189 T8190 nummod 1,5
R2118 T8190 T8188 nummod 5,triphosphate
R2120 T8191 T8190 punct ",",5
R2121 T8192 T8190 nummod 4,5
R2122 T8193 T8190 punct ",",5
R2124 T8194 T8188 punct -,triphosphate
R2125 T8195 T8196 punct [,9
R2126 T8196 T8173 parataxis 9,facilitates
R2128 T8197 T8196 punct ],9
R2129 T8198 T8167 punct .,coupled
R2131 T8200 T8201 nsubjpass Itpr1,enriched
R2133 T8202 T8201 auxpass is,enriched
R2134 T8203 T8201 prep in,enriched
R2135 T8204 T8205 det the,cells
R2137 T8205 T8203 pobj cells,in
R2138 T8206 T8205 compound Purkinje,cells
R2139 T8207 T8205 prep of,cells
R2141 T8208 T8209 det the,cerebellum
R2142 T8209 T8207 pobj cerebellum,of
R2143 T8210 T8211 punct [,4
R2145 T8211 T8201 parataxis 4,enriched
R2146 T8212 T8211 punct ],4
R2147 T8213 T8201 punct .,enriched
R2150 T8215 T8216 compound ITPR1,mutations
R2152 T8216 T8217 nsubj mutations,have
R2154 T8218 T8219 amod more,one
R2155 T8219 T8221 nummod one,mechanism
R2156 T8220 T8219 quantmod than,one
R2157 T8221 T8217 dobj mechanism,have
R2159 T8222 T8221 amod potential,mechanism
R2160 T8223 T8221 amod pathogenic,mechanism
R2161 T8224 T8217 punct .,have
R2163 T8226 T8227 advmod First,is
R2165 T8228 T8227 punct ", ",is
R2166 T8229 T8230 det the,disease
R2167 T8230 T8231 nsubj disease,be
R2168 T8231 T8227 ccomp be,is
R2170 T8232 T8231 aux may,be
R2171 T8233 T8234 det a,result
R2172 T8234 T8231 attr result,be
R2173 T8235 T8234 prep of,result
R2175 T8236 T8235 pobj haploinsufficiency,of
R2176 T8237 T8236 prep at,haploinsufficiency
R2177 T8277 T8278 advmod much,shorter
R2178 T8238 T8237 pobj ITPR1,at
R2179 T8239 T8227 punct ;,is
R2180 T8240 T8241 det this,concept
R2181 T8241 T8227 nsubj concept,is
R2182 T8278 T8276 amod shorter,span
R2183 T8242 T8227 acomp consistent,is
R2184 T8243 T8242 prep with,consistent
R2185 T8244 T8245 det the,observation
R2186 T8279 T8276 compound life,span
R2187 T8245 T8243 pobj observation,with
R2188 T8246 T8247 mark that,leads
R2189 T8247 T8245 acl leads,observation
R2190 T8280 T8276 prep of,span
R2191 T8248 T8249 amod heterozygous,deletion
R2192 T8249 T8247 nsubj deletion,leads
R2193 T8250 T8247 prep to,leads
R2194 T8281 T8282 det the,mouse
R2195 T8251 T8252 det a,disorder
R2196 T8252 T8250 pobj disorder,to
R2197 T8282 T8280 pobj mouse,of
R2198 T8253 T8254 amod later,onset
R2199 T8254 T8252 compound onset,disorder
R2200 T8255 T8247 prep in,leads
R2201 T8283 T8227 punct .,is
R2202 T8256 T8255 pobj humans,in
R2203 T8257 T8247 punct ", ",leads
R2204 T8285 T8286 advmod Second,failed
R2205 T8258 T8259 mark whereas,leads
R2206 T8259 T8247 advcl leads,leads
R2207 T8260 T8261 amod homozygous,deletion
R2208 T8261 T8259 nsubj deletion,leads
R2209 T8262 T8261 prep in,deletion
R2210 T8263 T8262 pobj mice,in
R2211 T8287 T8286 punct ", ",failed
R2212 T8264 T8259 prep to,leads
R2213 T8265 T8266 det an,disorder
R2214 T8266 T8264 pobj disorder,to
R2215 T8288 T8289 nsubj we,rule
R2216 T8267 T8268 amod early,onset
R2217 T8268 T8266 compound onset,disorder
R2218 T8269 T8266 punct ", ",disorder
R2219 T8270 T8266 amod able,disorder
R2220 T8271 T8272 aux to,expressed
R2221 T8272 T8270 xcomp expressed,able
R2222 T8289 T8286 ccomp rule,failed
R2223 T8273 T8272 auxpass be,expressed
R2224 T8274 T8272 prep within,expressed
R2225 T8275 T8276 det the,span
R2226 T8290 T8289 aux can,rule
R2227 T8276 T8274 pobj span,within
R2228 T8291 T8289 neg not,rule
R2229 T8292 T8289 prt out,rule
R2231 T8293 T8294 det the,existence
R2234 T8294 T8289 dobj existence,rule
R2235 T8295 T8294 prep of,existence
R2237 T8296 T8297 det an,site
R2241 T8297 T8295 pobj site,of
R2245 T8298 T8297 amod alternate,site
R2248 T8299 T8297 compound start,site
R2250 T8300 T8297 prep for,site
R2254 T8301 T8300 pobj ITPR1,for
R2257 T8302 T8303 dep that,result
R2261 T8303 T8297 relcl result,site
R2265 T8304 T8303 aux may,result
R2268 T8305 T8303 prep in,result
R2274 T8306 T8307 det a,product
R2278 T8307 T8305 pobj product,in
R2282 T8308 T8309 dep that,confers
R2285 T8309 T8307 relcl confers,product
R2289 T8310 T8311 det a,gain
R2293 T8311 T8309 dobj gain,confers
R2298 T8312 T8311 amod pathogenic,gain
R2301 T8313 T8311 prep of,gain
R2305 T8314 T8313 pobj function,of
R2309 T8315 T8309 prep to,confers
R2312 T8316 T8317 det the,protein
R2315 T8317 T8315 pobj protein,to
R2317 T8318 T8286 punct ;,failed
R2324 T8319 T8286 advmod however,failed
R2329 T8320 T8286 punct ", ",failed
R2333 T8321 T8322 compound Western,blot
R2336 T8322 T8323 compound blot,analysis
R2340 T8323 T8286 nsubj analysis,failed
R2342 T8324 T8323 prep of,analysis
R2345 T8325 T8324 pobj cells,of
R2347 T8326 T8325 acl derived,cells
R2348 T8327 T8326 prep from,derived
R2351 T8328 T8329 amod affected,members
R2354 T8329 T8327 pobj members,from
R2358 T8330 T8331 compound AUS1,family
R2360 T8331 T8329 compound family,members
R2361 T8332 T8323 punct ", ",analysis
R2363 T8333 T8334 dep which,performed
R2367 T8334 T8323 relcl performed,analysis
R2369 T8335 T8334 auxpass was,performed
R2372 T8336 T8334 advcl using,performed
R2373 T8337 T8338 det an,antibody
R2374 T8338 T8336 dobj antibody,using
R2376 T8339 T8338 acl raised,antibody
R2379 T8340 T8339 prep against,raised
R2383 T8341 T8342 det the,portion
R2386 T8342 T8340 pobj portion,against
R2389 T8343 T8344 npadvmod C,terminal
R2392 T8344 T8342 amod terminal,portion
R2396 T8345 T8344 punct -,terminal
R2400 T8346 T8342 prep of,portion
R2403 T8347 T8346 pobj ITPR1,of
R2407 T8348 T8286 punct ", ",failed
R2411 T8349 T8350 aux to,identify
R2414 T8350 T8286 xcomp identify,failed
R2418 T8351 T8352 det any,products
R2421 T8352 T8350 dobj products,identify
R2428 T8353 T8354 npadvmod disease,specific
R2431 T8354 T8352 amod specific,products
R2435 T8355 T8354 punct -,specific
R2439 T8356 T8357 amod truncated,protein
R2442 T8357 T8352 compound protein,products
R2445 T8358 T8286 punct .,failed
R2448 T8360 T8361 advmod Clearly,help
R2453 T8362 T8361 punct ", ",help
R2458 T8363 T8364 det the,identification
R2460 T8364 T8361 nsubj identification,help
R2462 T8365 T8364 prep of,identification
R2463 T8366 T8367 amod distinct,mutations
R2467 T8367 T8365 pobj mutations,of
R2470 T8368 T8367 compound ITPR1,mutations
R2473 T8369 T8367 acl underlying,mutations
R2479 T8370 T8369 dobj SCA15,underlying
R2483 T8371 T8361 aux will,help
R2487 T8372 T8361 xcomp elucidate,help
R2490 T8373 T8374 det the,mechanism
R2494 T8374 T8372 dobj mechanism,elucidate
R2498 T8375 T8374 amod pathogenic,mechanism
R2501 T8376 T8374 prep of,mechanism
R2506 T8377 T8378 det this,disorder
R2510 T8378 T8376 pobj disorder,of
R2512 T8379 T8361 punct .,help

2_test

Id Subject Object Predicate Lexical cue
17590087-10426189-85657855 400-401 10426189 denotes 9
17590087-8538767-85657856 463-464 8538767 denotes 4
T70545 400-401 10426189 denotes 9
T38629 463-464 8538767 denotes 4