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PMC:2806624 / 2043-2342 JSONTXT

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pmc-enju-pas

Id Subject Object Predicate Lexical cue
T1391 0-1 DT denotes A
T1392 2-13 JJ denotes spontaneous
T1393 14-22 NN denotes mutation
T1394 23-25 IN denotes of
T1395 26-29 DT denotes the
T1396 30-49 NN denotes X-linked Foxp3 gene
T1397 50-64 NN denotes in scurfy mice
T1398 65-71 VB denotes causes
T1399 72-74 DT denotes an
T1400 75-90 JJ denotes autoimmune-like
T1401 91-98 NN denotes disease
T1402 98-99 -COMMA- denotes ,
T1403 100-107 IN denotes whereas
T1404 108-111 DT denotes the
T1405 112-120 NN denotes mutation
T1406 121-123 IN denotes in
T1407 124-130 NN denotes humans
T1408 131-136 VB denotes leads
T1409 137-139 TO denotes to
T1410 140-159 NN denotes immunodysregulation
T1411 159-160 -COMMA- denotes ,
T1412 161-179 NN denotes polyendocrinopathy
T1413 179-180 -COMMA- denotes ,
T1414 181-192 NN denotes enteropathy
T1415 192-193 -COMMA- denotes ,
T1416 194-197 CC denotes and
T1417 198-206 JJ denotes X-linked
T1418 207-215 NN denotes syndrome
T1419 216-220 WDT denotes that
T1420 221-223 VB denotes is
T1421 224-228 RB denotes also
T1422 229-230 DT denotes a
T1423 231-237 JJ denotes severe
T1424 238-248 JJ denotes multiorgan
T1425 249-259 JJ denotes autoimmune
T1426 260-267 NN denotes disease
T1427 268-272 IN denotes with
T1428 273-282 NN denotes hyper-IgE
T1429 283-284 -LRB- denotes (
T1430 284-291 NNP denotes Ziegler
T1431 291-292 -COMMA- denotes ,
T1432 293-297 CD denotes 2006
T1433 297-298 -RRB- denotes )
R973 T1393 T1391 arg1Of mutation,A
R974 T1393 T1392 arg1Of mutation,spontaneous
R975 T1393 T1394 arg1Of mutation,of
R976 T1393 T1398 arg1Of mutation,causes
R977 T1397 T1394 arg2Of in scurfy mice,of
R978 T1397 T1395 arg1Of in scurfy mice,the
R979 T1397 T1396 arg1Of in scurfy mice,X-linked Foxp3 gene
R980 T1398 T1403 arg1Of causes,whereas
R981 T1401 T1398 arg2Of disease,causes
R982 T1401 T1399 arg1Of disease,an
R983 T1401 T1400 arg1Of disease,autoimmune-like
R984 T1403 T1402 arg1Of whereas,","
R986 T1405 T1404 arg1Of mutation,the
R987 T1405 T1406 arg1Of mutation,in
R988 T1405 T1408 arg1Of mutation,leads
R989 T1407 T1406 arg2Of humans,in
R990 T1408 T1403 arg2Of leads,whereas
R991 T1408 T1409 arg1Of leads,to
R992 T1410 T1411 arg1Of immunodysregulation,","
R993 T1411 T1413 arg1Of ",",","
R994 T1412 T1411 arg2Of polyendocrinopathy,","
R995 T1413 T1416 arg1Of ",",and
R996 T1414 T1413 arg2Of enteropathy,","
R997 T1416 T1409 arg2Of and,to
R998 T1416 T1415 arg1Of and,","
R999 T1418 T1416 arg2Of syndrome,and
R1000 T1418 T1417 arg1Of syndrome,X-linked
R1001 T1418 T1419 arg1Of syndrome,that
R1002 T1418 T1420 arg1Of syndrome,is
R1003 T1420 T1421 arg1Of is,also
R1004 T1420 T1429 arg1Of is,(
R1005 T1426 T1420 arg2Of disease,is
R1006 T1426 T1422 arg1Of disease,a
R1007 T1426 T1423 arg1Of disease,severe
R1008 T1426 T1424 arg1Of disease,multiorgan
R1009 T1426 T1425 arg1Of disease,autoimmune
R1010 T1426 T1427 arg1Of disease,with
R1011 T1428 T1427 arg2Of hyper-IgE,with
R1012 T1430 T1429 arg2Of Ziegler,(
R1013 T1430 T1431 arg1Of Ziegler,","
R1014 T1430 T1432 arg1Of Ziegler,2006
R1015 T1433 T1429 arg3Of ),(

bionlp-st-ge-2016-spacy-parsed

Id Subject Object Predicate Lexical cue
T2212 0-1 DT denotes A
T2213 2-13 JJ denotes spontaneous
T2214 14-22 NN denotes mutation
T2215 23-25 IN denotes of
T2216 26-29 DT denotes the
T2217 30-49 JJ denotes X-linked Foxp3 gene
T2218 50-64 NN denotes in scurfy mice
T2219 65-71 VBZ denotes causes
T2220 72-74 DT denotes an
T2221 75-90 JJ denotes autoimmune-like
T2222 91-98 NN denotes disease
T2223 98-99 , denotes ,
T2224 100-107 IN denotes whereas
T2225 108-111 DT denotes the
T2226 112-120 NN denotes mutation
T2227 121-123 IN denotes in
T2228 124-130 NNS denotes humans
T2229 131-136 VBZ denotes leads
T2230 137-139 TO denotes to
T2231 140-159 NN denotes immunodysregulation
T2232 159-160 , denotes ,
T2233 161-179 NN denotes polyendocrinopathy
T2234 179-180 , denotes ,
T2235 181-192 NN denotes enteropathy
T2236 192-193 , denotes ,
T2237 194-197 CC denotes and
T2238 198-206 JJ denotes X-linked
T2239 207-215 NN denotes syndrome
T2240 216-220 WDT denotes that
T2241 221-223 VBZ denotes is
T2242 224-228 RB denotes also
T2243 229-230 DT denotes a
T2244 231-237 JJ denotes severe
T2245 238-248 JJ denotes multiorgan
T2246 249-259 JJ denotes autoimmune
T2247 260-267 NN denotes disease
T2248 268-272 IN denotes with
T2249 273-282 NNP denotes hyper-IgE
T2250 283-284 -LRB- denotes (
T2251 284-291 NNP denotes Ziegler
T2252 291-292 , denotes ,
T2253 293-297 CD denotes 2006
T2254 297-298 -RRB- denotes )
T2255 298-299 . denotes .
R1683 T2246 T2247 amod autoimmune,disease
R1685 T2247 T2241 attr disease,is
R1689 T2248 T2247 prep with,disease
R1693 T2249 T2248 pobj hyper-IgE,with
R1696 T2250 T2251 punct (,Ziegler
R1700 T2251 T2249 appos Ziegler,hyper-IgE
R1704 T2252 T2251 punct ",",Ziegler
R1711 T2253 T2251 npadvmod 2006,Ziegler
R1716 T2254 T2251 punct ),Ziegler
R1721 T2255 T2219 punct .,causes
R1723 T2212 T2214 det A,mutation
R1725 T2213 T2214 amod spontaneous,mutation
R1726 T2214 T2219 nsubj mutation,causes
R1727 T2215 T2214 prep of,mutation
R1729 T2216 T2218 det the,in scurfy mice
R1730 T2217 T2218 amod X-linked Foxp3 gene,in scurfy mice
R1731 T2218 T2215 pobj in scurfy mice,of
R1733 T2219 T2219 ROOT causes,causes
R1734 T2220 T2222 det an,disease
R1735 T2221 T2222 amod autoimmune-like,disease
R1737 T2222 T2219 dobj disease,causes
R1738 T2223 T2219 punct ",",causes
R1739 T2224 T2229 mark whereas,leads
R1740 T2225 T2226 det the,mutation
R1741 T2226 T2229 nsubj mutation,leads
R1742 T2227 T2226 prep in,mutation
R1743 T2228 T2227 pobj humans,in
R1745 T2229 T2219 advcl leads,causes
R1746 T2230 T2229 prep to,leads
R1747 T2231 T2230 pobj immunodysregulation,to
R1749 T2232 T2231 punct ",",immunodysregulation
R1750 T2233 T2231 conj polyendocrinopathy,immunodysregulation
R1751 T2234 T2233 punct ",",polyendocrinopathy
R1753 T2235 T2233 conj enteropathy,polyendocrinopathy
R1754 T2236 T2235 punct ",",enteropathy
R1755 T2237 T2235 cc and,enteropathy
R1756 T2238 T2239 compound X-linked,syndrome
R1757 T2239 T2235 conj syndrome,enteropathy
R1758 T2240 T2241 nsubj that,is
R1760 T2241 T2239 relcl is,syndrome
R1761 T2242 T2241 advmod also,is
R1762 T2243 T2247 det a,disease
R1764 T2244 T2247 amod severe,disease
R1766 T2245 T2247 amod multiorgan,disease

sentences

Id Subject Object Predicate Lexical cue
T14 0-299 Sentence denotes A spontaneous mutation of the X-linked Foxp3 gene in scurfy mice causes an autoimmune-like disease, whereas the mutation in humans leads to immunodysregulation, polyendocrinopathy, enteropathy, and X-linked syndrome that is also a severe multiorgan autoimmune disease with hyper-IgE (Ziegler, 2006).

events-check-again

Id Subject Object Predicate Lexical cue
T3212 39-44 Protein denotes Foxp3

bionlp-st-ge-2016-reference-tees

Id Subject Object Predicate Lexical cue
T3033 30-49 Protein denotes X-linked Foxp3 gene

bionlp-st-ge-2016-reference

Id Subject Object Predicate Lexical cue
T1202 39-44 Protein denotes Foxp3

test2

Id Subject Object Predicate Lexical cue
T1120 32-49 Protein denotes linked Foxp3 gene