| Id |
Subject |
Object |
Predicate |
Lexical cue |
| T781 |
0-3 |
NN |
denotes |
XPD |
| T782 |
4-11 |
VBZ |
denotes |
encodes |
| T783 |
12-15 |
CD |
denotes |
one |
| T784 |
16-18 |
IN |
denotes |
of |
| T785 |
19-22 |
DT |
denotes |
the |
| T787 |
23-26 |
CD |
denotes |
two |
| T788 |
27-35 |
NN |
denotes |
helicase |
| T786 |
36-46 |
NNS |
denotes |
components |
| T789 |
47-49 |
IN |
denotes |
of |
| T790 |
50-55 |
JJ |
denotes |
basal |
| T792 |
56-69 |
NN |
denotes |
transcription |
| T793 |
69-70 |
HYPH |
denotes |
/ |
| T794 |
70-73 |
NN |
denotes |
DNA |
| T795 |
74-80 |
NN |
denotes |
repair |
| T796 |
81-87 |
NN |
denotes |
factor |
| T791 |
88-91 |
NN |
denotes |
IIH |
| T797 |
92-93 |
-LRB- |
denotes |
( |
| T798 |
93-98 |
NN |
denotes |
TFIIH |
| T799 |
98-99 |
-RRB- |
denotes |
) |
| T800 |
99-101 |
, |
denotes |
, |
| T801 |
101-102 |
DT |
denotes |
a |
| T803 |
103-106 |
CD |
denotes |
ten |
| T805 |
106-107 |
HYPH |
denotes |
- |
| T804 |
107-114 |
NN |
denotes |
subunit |
| T806 |
114-116 |
, |
denotes |
, |
| T807 |
116-131 |
JJ |
denotes |
multifunctional |
| T802 |
132-139 |
NN |
denotes |
complex |
| T808 |
140-144 |
WDT |
denotes |
that |
| T809 |
145-147 |
VBZ |
denotes |
is |
| T810 |
148-157 |
JJ |
denotes |
essential |
| T811 |
158-161 |
IN |
denotes |
for |
| T812 |
162-170 |
JJ |
denotes |
multiple |
| T813 |
171-180 |
NNS |
denotes |
processes |
| T814 |
180-182 |
, |
denotes |
, |
| T815 |
182-191 |
VBG |
denotes |
including |
| T816 |
192-197 |
JJ |
denotes |
basal |
| T818 |
198-211 |
NN |
denotes |
transcription |
| T817 |
212-222 |
NN |
denotes |
initiation |
| T819 |
223-226 |
CC |
denotes |
and |
| T820 |
227-230 |
NN |
denotes |
DNA |
| T822 |
231-237 |
NN |
denotes |
damage |
| T821 |
238-244 |
NN |
denotes |
repair |
| T823 |
245-248 |
IN |
denotes |
via |
| T824 |
249-252 |
DT |
denotes |
the |
| T826 |
253-263 |
NN |
denotes |
nucleotide |
| T828 |
264-272 |
NN |
denotes |
excision |
| T827 |
273-279 |
NN |
denotes |
repair |
| T829 |
280-281 |
-LRB- |
denotes |
( |
| T830 |
281-284 |
NN |
denotes |
NER |
| T831 |
284-285 |
-RRB- |
denotes |
) |
| T825 |
286-293 |
NN |
denotes |
pathway |
| T832 |
294-295 |
-LRB- |
denotes |
[ |
| T834 |
295-296 |
CD |
denotes |
6 |
| T835 |
296-297 |
, |
denotes |
, |
| T833 |
297-298 |
CD |
denotes |
7 |
| T836 |
298-299 |
-RRB- |
denotes |
] |
| T837 |
299-300 |
. |
denotes |
. |
| T838 |
300-530 |
sentence |
denotes |
Alterations in XPD resulting in defective TFIIH function are associated with UV-sensitive, multisystem disorders including xeroderma pigmentosum (XP), XP combined with Cockayne syndrome (CS), and trichothiodystrophy (TTD) [8–10]. |
| T839 |
301-312 |
NNS |
denotes |
Alterations |
| T841 |
313-315 |
IN |
denotes |
in |
| T842 |
316-319 |
NN |
denotes |
XPD |
| T843 |
320-329 |
VBG |
denotes |
resulting |
| T844 |
330-332 |
IN |
denotes |
in |
| T845 |
333-342 |
JJ |
denotes |
defective |
| T847 |
343-348 |
NN |
denotes |
TFIIH |
| T846 |
349-357 |
NN |
denotes |
function |
| T848 |
358-361 |
VBP |
denotes |
are |
| T840 |
362-372 |
VBN |
denotes |
associated |
| T849 |
373-377 |
IN |
denotes |
with |
| T850 |
378-380 |
NN |
denotes |
UV |
| T852 |
380-381 |
HYPH |
denotes |
- |
| T851 |
381-390 |
JJ |
denotes |
sensitive |
| T854 |
390-392 |
, |
denotes |
, |
| T855 |
392-403 |
JJ |
denotes |
multisystem |
| T853 |
404-413 |
NNS |
denotes |
disorders |
| T856 |
414-423 |
VBG |
denotes |
including |
| T857 |
424-433 |
NN |
denotes |
xeroderma |
| T858 |
434-445 |
NN |
denotes |
pigmentosum |
| T859 |
446-447 |
-LRB- |
denotes |
( |
| T860 |
447-449 |
NN |
denotes |
XP |
| T861 |
449-450 |
-RRB- |
denotes |
) |
| T862 |
450-452 |
, |
denotes |
, |
| T863 |
452-454 |
NN |
denotes |
XP |
| T864 |
455-463 |
VBN |
denotes |
combined |
| T865 |
464-468 |
IN |
denotes |
with |
| T866 |
469-477 |
NN |
denotes |
Cockayne |
| T867 |
478-486 |
NN |
denotes |
syndrome |
| T868 |
487-488 |
-LRB- |
denotes |
( |
| T869 |
488-490 |
NN |
denotes |
CS |
| T870 |
490-491 |
-RRB- |
denotes |
) |
| T871 |
491-493 |
, |
denotes |
, |
| T872 |
493-496 |
CC |
denotes |
and |
| T873 |
497-516 |
NN |
denotes |
trichothiodystrophy |
| T874 |
517-518 |
-LRB- |
denotes |
( |
| T875 |
518-521 |
NN |
denotes |
TTD |
| T876 |
521-522 |
-RRB- |
denotes |
) |
| T877 |
523-524 |
-LRB- |
denotes |
[ |
| T878 |
524-525 |
CD |
denotes |
8 |
| T879 |
525-526 |
SYM |
denotes |
– |
| T880 |
526-528 |
CD |
denotes |
10 |
| T881 |
528-529 |
-RRB- |
denotes |
] |
| T882 |
529-530 |
. |
denotes |
. |
| T883 |
530-642 |
sentence |
denotes |
XP is marked by sun-induced pigmentation anomalies and a greater than 1,000-fold elevation in skin cancer risk. |
| T884 |
531-533 |
NN |
denotes |
XP |
| T886 |
534-536 |
VBZ |
denotes |
is |
| T885 |
537-543 |
VBN |
denotes |
marked |
| T887 |
544-546 |
IN |
denotes |
by |
| T888 |
547-550 |
NN |
denotes |
sun |
| T890 |
550-551 |
HYPH |
denotes |
- |
| T889 |
551-558 |
VBN |
denotes |
induced |
| T892 |
559-571 |
NN |
denotes |
pigmentation |
| T891 |
572-581 |
NNS |
denotes |
anomalies |
| T893 |
582-585 |
CC |
denotes |
and |
| T894 |
586-587 |
DT |
denotes |
a |
| T896 |
588-595 |
JJR |
denotes |
greater |
| T898 |
596-600 |
IN |
denotes |
than |
| T897 |
601-606 |
CD |
denotes |
1,000 |
| T900 |
606-607 |
HYPH |
denotes |
- |
| T899 |
607-611 |
RB |
denotes |
fold |
| T895 |
612-621 |
NN |
denotes |
elevation |
| T901 |
622-624 |
IN |
denotes |
in |
| T902 |
625-629 |
NN |
denotes |
skin |
| T903 |
630-636 |
NN |
denotes |
cancer |
| T904 |
637-641 |
NN |
denotes |
risk |
| T905 |
641-642 |
. |
denotes |
. |
| T906 |
642-732 |
sentence |
denotes |
Severe cases can also present with growth retardation and primary neurodegeneration [11]. |
| T907 |
643-649 |
JJ |
denotes |
Severe |
| T908 |
650-655 |
NNS |
denotes |
cases |
| T910 |
656-659 |
MD |
denotes |
can |
| T911 |
660-664 |
RB |
denotes |
also |
| T909 |
665-672 |
VB |
denotes |
present |
| T912 |
673-677 |
IN |
denotes |
with |
| T913 |
678-684 |
NN |
denotes |
growth |
| T914 |
685-696 |
NN |
denotes |
retardation |
| T915 |
697-700 |
CC |
denotes |
and |
| T916 |
701-708 |
JJ |
denotes |
primary |
| T917 |
709-726 |
NN |
denotes |
neurodegeneration |
| T918 |
727-728 |
-LRB- |
denotes |
[ |
| T919 |
728-730 |
CD |
denotes |
11 |
| T920 |
730-731 |
-RRB- |
denotes |
] |
| T921 |
731-732 |
. |
denotes |
. |
| T922 |
732-967 |
sentence |
denotes |
CS and TTD, on the other hand, are segmental progeroid disorders characterised by progressive post-natal growth failure and primary demyelination resulting in severe neurodysfunction, but without a clear cancer predisposition [12–15]. |
| T923 |
733-735 |
NN |
denotes |
CS |
| T925 |
736-739 |
CC |
denotes |
and |
| T926 |
740-743 |
NN |
denotes |
TTD |
| T927 |
743-745 |
, |
denotes |
, |
| T928 |
745-747 |
IN |
denotes |
on |
| T929 |
748-751 |
DT |
denotes |
the |
| T931 |
752-757 |
JJ |
denotes |
other |
| T930 |
758-762 |
NN |
denotes |
hand |
| T932 |
762-764 |
, |
denotes |
, |
| T924 |
764-767 |
VBP |
denotes |
are |
| T933 |
768-777 |
JJ |
denotes |
segmental |
| T935 |
778-787 |
JJ |
denotes |
progeroid |
| T934 |
788-797 |
NNS |
denotes |
disorders |
| T936 |
798-811 |
VBN |
denotes |
characterised |
| T937 |
812-814 |
IN |
denotes |
by |
| T938 |
815-826 |
JJ |
denotes |
progressive |
| T940 |
827-837 |
JJ |
denotes |
post-natal |
| T941 |
838-844 |
NN |
denotes |
growth |
| T939 |
845-852 |
NN |
denotes |
failure |
| T942 |
853-856 |
CC |
denotes |
and |
| T943 |
857-864 |
JJ |
denotes |
primary |
| T944 |
865-878 |
NN |
denotes |
demyelination |
| T945 |
879-888 |
VBG |
denotes |
resulting |
| T946 |
889-891 |
IN |
denotes |
in |
| T947 |
892-898 |
JJ |
denotes |
severe |
| T948 |
899-915 |
NN |
denotes |
neurodysfunction |
| T949 |
915-917 |
, |
denotes |
, |
| T950 |
917-920 |
CC |
denotes |
but |
| T951 |
921-928 |
IN |
denotes |
without |
| T952 |
929-930 |
DT |
denotes |
a |
| T954 |
931-936 |
JJ |
denotes |
clear |
| T955 |
937-943 |
NN |
denotes |
cancer |
| T953 |
944-958 |
NN |
denotes |
predisposition |
| T956 |
959-960 |
-LRB- |
denotes |
[ |
| T957 |
960-962 |
CD |
denotes |
12 |
| T958 |
962-963 |
SYM |
denotes |
– |
| T959 |
963-965 |
CD |
denotes |
15 |
| T960 |
965-966 |
-RRB- |
denotes |
] |
| T961 |
966-967 |
. |
denotes |
. |
| T962 |
967-1155 |
sentence |
denotes |
Patients with TTD additionally display hallmark sulphur-deficient brittle hair and nails and scaling skin [13], resulting from a basal transcription defect in specific cell types [16,17]. |
| T963 |
968-976 |
NNS |
denotes |
Patients |
| T965 |
977-981 |
IN |
denotes |
with |
| T966 |
982-985 |
NN |
denotes |
TTD |
| T967 |
986-998 |
RB |
denotes |
additionally |
| T964 |
999-1006 |
VBP |
denotes |
display |
| T968 |
1007-1015 |
NN |
denotes |
hallmark |
| T970 |
1016-1023 |
NN |
denotes |
sulphur |
| T972 |
1023-1024 |
HYPH |
denotes |
- |
| T971 |
1024-1033 |
JJ |
denotes |
deficient |
| T973 |
1034-1041 |
JJ |
denotes |
brittle |
| T969 |
1042-1046 |
NN |
denotes |
hair |
| T974 |
1047-1050 |
CC |
denotes |
and |
| T975 |
1051-1056 |
NNS |
denotes |
nails |
| T976 |
1057-1060 |
CC |
denotes |
and |
| T977 |
1061-1068 |
JJ |
denotes |
scaling |
| T978 |
1069-1073 |
NN |
denotes |
skin |
| T979 |
1074-1075 |
-LRB- |
denotes |
[ |
| T980 |
1075-1077 |
CD |
denotes |
13 |
| T981 |
1077-1078 |
-RRB- |
denotes |
] |
| T982 |
1078-1080 |
, |
denotes |
, |
| T983 |
1080-1089 |
VBG |
denotes |
resulting |
| T984 |
1090-1094 |
IN |
denotes |
from |
| T985 |
1095-1096 |
DT |
denotes |
a |
| T987 |
1097-1102 |
JJ |
denotes |
basal |
| T988 |
1103-1116 |
NN |
denotes |
transcription |
| T986 |
1117-1123 |
NN |
denotes |
defect |
| T989 |
1124-1126 |
IN |
denotes |
in |
| T990 |
1127-1135 |
JJ |
denotes |
specific |
| T992 |
1136-1140 |
NN |
denotes |
cell |
| T991 |
1141-1146 |
NNS |
denotes |
types |
| T993 |
1147-1148 |
-LRB- |
denotes |
[ |
| T995 |
1148-1150 |
CD |
denotes |
16 |
| T996 |
1150-1151 |
, |
denotes |
, |
| T994 |
1151-1153 |
CD |
denotes |
17 |
| T997 |
1153-1154 |
-RRB- |
denotes |
] |
| T998 |
1154-1155 |
. |
denotes |
. |
| T999 |
1155-1321 |
sentence |
denotes |
A related disorder with the cancer predisposition of XP combined with the neurodevelopmental complications of CS (XPCS), although rare, has also been described [18]. |
| T1000 |
1156-1157 |
DT |
denotes |
A |
| T1002 |
1158-1165 |
JJ |
denotes |
related |
| T1001 |
1166-1174 |
NN |
denotes |
disorder |
| T1004 |
1175-1179 |
IN |
denotes |
with |
| T1005 |
1180-1183 |
DT |
denotes |
the |
| T1007 |
1184-1190 |
NN |
denotes |
cancer |
| T1006 |
1191-1205 |
NN |
denotes |
predisposition |
| T1008 |
1206-1208 |
IN |
denotes |
of |
| T1009 |
1209-1211 |
NN |
denotes |
XP |
| T1010 |
1212-1220 |
VBN |
denotes |
combined |
| T1011 |
1221-1225 |
IN |
denotes |
with |
| T1012 |
1226-1229 |
DT |
denotes |
the |
| T1014 |
1230-1248 |
JJ |
denotes |
neurodevelopmental |
| T1013 |
1249-1262 |
NNS |
denotes |
complications |
| T1015 |
1263-1265 |
IN |
denotes |
of |
| T1016 |
1266-1268 |
NN |
denotes |
CS |
| T1017 |
1269-1270 |
-LRB- |
denotes |
( |
| T1018 |
1270-1274 |
NN |
denotes |
XPCS |
| T1019 |
1274-1275 |
-RRB- |
denotes |
) |
| T1020 |
1275-1277 |
, |
denotes |
, |
| T1021 |
1277-1285 |
IN |
denotes |
although |
| T1022 |
1286-1290 |
JJ |
denotes |
rare |
| T1023 |
1290-1292 |
, |
denotes |
, |
| T1024 |
1292-1295 |
VBZ |
denotes |
has |
| T1025 |
1296-1300 |
RB |
denotes |
also |
| T1026 |
1301-1305 |
VBN |
denotes |
been |
| T1003 |
1306-1315 |
VBN |
denotes |
described |
| T1027 |
1316-1317 |
-LRB- |
denotes |
[ |
| T1028 |
1317-1319 |
CD |
denotes |
18 |
| T1029 |
1319-1320 |
-RRB- |
denotes |
] |
| T1030 |
1320-1321 |
. |
denotes |
. |
| R450 |
T781 |
T782 |
nsubj |
XPD,encodes |
| R451 |
T783 |
T782 |
dobj |
one,encodes |
| R452 |
T784 |
T783 |
prep |
of,one |
| R453 |
T785 |
T786 |
det |
the,components |
| R454 |
T786 |
T784 |
pobj |
components,of |
| R455 |
T787 |
T786 |
nummod |
two,components |
| R456 |
T788 |
T786 |
compound |
helicase,components |
| R457 |
T789 |
T786 |
prep |
of,components |
| R458 |
T790 |
T791 |
amod |
basal,IIH |
| R459 |
T791 |
T789 |
pobj |
IIH,of |
| R460 |
T792 |
T791 |
nmod |
transcription,IIH |
| R461 |
T793 |
T792 |
punct |
/,transcription |
| R462 |
T794 |
T795 |
compound |
DNA,repair |
| R463 |
T795 |
T792 |
appos |
repair,transcription |
| R464 |
T796 |
T791 |
compound |
factor,IIH |
| R465 |
T797 |
T791 |
punct |
(,IIH |
| R466 |
T798 |
T791 |
appos |
TFIIH,IIH |
| R467 |
T799 |
T783 |
punct |
),one |
| R468 |
T800 |
T783 |
punct |
", ",one |
| R469 |
T801 |
T802 |
det |
a,complex |
| R470 |
T802 |
T783 |
appos |
complex,one |
| R471 |
T803 |
T804 |
nummod |
ten,subunit |
| R472 |
T804 |
T802 |
nmod |
subunit,complex |
| R473 |
T805 |
T804 |
punct |
-,subunit |
| R474 |
T806 |
T802 |
punct |
", ",complex |
| R475 |
T807 |
T802 |
amod |
multifunctional,complex |
| R476 |
T808 |
T809 |
dep |
that,is |
| R477 |
T809 |
T802 |
relcl |
is,complex |
| R478 |
T810 |
T809 |
acomp |
essential,is |
| R479 |
T811 |
T810 |
prep |
for,essential |
| R480 |
T812 |
T813 |
amod |
multiple,processes |
| R481 |
T813 |
T811 |
pobj |
processes,for |
| R482 |
T814 |
T813 |
punct |
", ",processes |
| R483 |
T815 |
T813 |
prep |
including,processes |
| R484 |
T816 |
T817 |
amod |
basal,initiation |
| R485 |
T817 |
T815 |
pobj |
initiation,including |
| R486 |
T818 |
T817 |
compound |
transcription,initiation |
| R487 |
T819 |
T817 |
cc |
and,initiation |
| R488 |
T820 |
T821 |
compound |
DNA,repair |
| R489 |
T821 |
T817 |
conj |
repair,initiation |
| R490 |
T822 |
T821 |
compound |
damage,repair |
| R491 |
T823 |
T821 |
prep |
via,repair |
| R492 |
T824 |
T825 |
det |
the,pathway |
| R493 |
T825 |
T823 |
pobj |
pathway,via |
| R494 |
T826 |
T827 |
nmod |
nucleotide,repair |
| R495 |
T827 |
T825 |
nmod |
repair,pathway |
| R496 |
T828 |
T827 |
nmod |
excision,repair |
| R497 |
T829 |
T827 |
punct |
(,repair |
| R498 |
T830 |
T827 |
appos |
NER,repair |
| R499 |
T831 |
T825 |
punct |
),pathway |
| R500 |
T832 |
T833 |
punct |
[,7 |
| R501 |
T833 |
T783 |
parataxis |
7,one |
| R502 |
T834 |
T833 |
nummod |
6,7 |
| R503 |
T835 |
T833 |
punct |
",",7 |
| R504 |
T836 |
T833 |
punct |
],7 |
| R505 |
T837 |
T782 |
punct |
.,encodes |
| R506 |
T839 |
T840 |
nsubjpass |
Alterations,associated |
| R507 |
T841 |
T839 |
prep |
in,Alterations |
| R508 |
T842 |
T841 |
pobj |
XPD,in |
| R509 |
T843 |
T839 |
acl |
resulting,Alterations |
| R510 |
T844 |
T843 |
prep |
in,resulting |
| R511 |
T845 |
T846 |
amod |
defective,function |
| R512 |
T846 |
T844 |
pobj |
function,in |
| R513 |
T847 |
T846 |
compound |
TFIIH,function |
| R514 |
T848 |
T840 |
auxpass |
are,associated |
| R515 |
T849 |
T840 |
prep |
with,associated |
| R516 |
T850 |
T851 |
npadvmod |
UV,sensitive |
| R517 |
T851 |
T853 |
amod |
sensitive,disorders |
| R518 |
T852 |
T851 |
punct |
-,sensitive |
| R519 |
T853 |
T849 |
pobj |
disorders,with |
| R520 |
T854 |
T853 |
punct |
", ",disorders |
| R521 |
T855 |
T853 |
amod |
multisystem,disorders |
| R522 |
T856 |
T853 |
prep |
including,disorders |
| R523 |
T857 |
T858 |
compound |
xeroderma,pigmentosum |
| R524 |
T858 |
T856 |
pobj |
pigmentosum,including |
| R525 |
T859 |
T858 |
punct |
(,pigmentosum |
| R526 |
T860 |
T858 |
appos |
XP,pigmentosum |
| R527 |
T861 |
T858 |
punct |
),pigmentosum |
| R528 |
T862 |
T858 |
punct |
", ",pigmentosum |
| R529 |
T863 |
T858 |
conj |
XP,pigmentosum |
| R530 |
T864 |
T863 |
acl |
combined,XP |
| R531 |
T865 |
T864 |
prep |
with,combined |
| R532 |
T866 |
T867 |
compound |
Cockayne,syndrome |
| R533 |
T867 |
T865 |
pobj |
syndrome,with |
| R534 |
T868 |
T867 |
punct |
(,syndrome |
| R535 |
T869 |
T867 |
appos |
CS,syndrome |
| R536 |
T870 |
T863 |
punct |
),XP |
| R537 |
T871 |
T863 |
punct |
", ",XP |
| R538 |
T872 |
T863 |
cc |
and,XP |
| R539 |
T873 |
T863 |
conj |
trichothiodystrophy,XP |
| R540 |
T874 |
T873 |
punct |
(,trichothiodystrophy |
| R541 |
T875 |
T873 |
appos |
TTD,trichothiodystrophy |
| R542 |
T876 |
T840 |
punct |
),associated |
| R543 |
T877 |
T878 |
punct |
[,8 |
| R544 |
T878 |
T840 |
parataxis |
8,associated |
| R545 |
T879 |
T880 |
punct |
–,10 |
| R546 |
T880 |
T878 |
prep |
10,8 |
| R547 |
T881 |
T878 |
punct |
],8 |
| R548 |
T882 |
T840 |
punct |
.,associated |
| R549 |
T884 |
T885 |
nsubjpass |
XP,marked |
| R550 |
T886 |
T885 |
auxpass |
is,marked |
| R551 |
T887 |
T885 |
agent |
by,marked |
| R552 |
T888 |
T889 |
npadvmod |
sun,induced |
| R553 |
T889 |
T891 |
amod |
induced,anomalies |
| R554 |
T890 |
T889 |
punct |
-,induced |
| R555 |
T891 |
T887 |
pobj |
anomalies,by |
| R556 |
T892 |
T891 |
compound |
pigmentation,anomalies |
| R557 |
T893 |
T891 |
cc |
and,anomalies |
| R558 |
T894 |
T895 |
det |
a,elevation |
| R559 |
T895 |
T891 |
conj |
elevation,anomalies |
| R560 |
T896 |
T897 |
amod |
greater,"1,000" |
| R561 |
T897 |
T899 |
quantmod |
"1,000",fold |
| R562 |
T898 |
T897 |
quantmod |
than,"1,000" |
| R563 |
T899 |
T895 |
nummod |
fold,elevation |
| R564 |
T900 |
T899 |
punct |
-,fold |
| R565 |
T901 |
T895 |
prep |
in,elevation |
| R566 |
T902 |
T903 |
compound |
skin,cancer |
| R567 |
T903 |
T904 |
compound |
cancer,risk |
| R568 |
T904 |
T901 |
pobj |
risk,in |
| R569 |
T905 |
T885 |
punct |
.,marked |
| R570 |
T907 |
T908 |
amod |
Severe,cases |
| R571 |
T908 |
T909 |
nsubj |
cases,present |
| R572 |
T910 |
T909 |
aux |
can,present |
| R573 |
T911 |
T909 |
advmod |
also,present |
| R574 |
T912 |
T909 |
prep |
with,present |
| R575 |
T913 |
T914 |
compound |
growth,retardation |
| R576 |
T914 |
T912 |
pobj |
retardation,with |
| R577 |
T915 |
T914 |
cc |
and,retardation |
| R578 |
T916 |
T917 |
amod |
primary,neurodegeneration |
| R579 |
T917 |
T914 |
conj |
neurodegeneration,retardation |
| R580 |
T918 |
T919 |
punct |
[,11 |
| R581 |
T919 |
T909 |
parataxis |
11,present |
| R582 |
T920 |
T919 |
punct |
],11 |
| R583 |
T921 |
T909 |
punct |
.,present |
| R584 |
T923 |
T924 |
nsubj |
CS,are |
| R585 |
T925 |
T923 |
cc |
and,CS |
| R586 |
T926 |
T923 |
conj |
TTD,CS |
| R587 |
T927 |
T924 |
punct |
", ",are |
| R588 |
T928 |
T924 |
prep |
on,are |
| R589 |
T929 |
T930 |
det |
the,hand |
| R590 |
T930 |
T928 |
pobj |
hand,on |
| R591 |
T931 |
T930 |
amod |
other,hand |
| R592 |
T932 |
T924 |
punct |
", ",are |
| R593 |
T933 |
T934 |
amod |
segmental,disorders |
| R594 |
T934 |
T924 |
attr |
disorders,are |
| R595 |
T935 |
T934 |
amod |
progeroid,disorders |
| R596 |
T936 |
T934 |
acl |
characterised,disorders |
| R597 |
T937 |
T936 |
agent |
by,characterised |
| R598 |
T938 |
T939 |
amod |
progressive,failure |
| R599 |
T939 |
T937 |
pobj |
failure,by |
| R600 |
T940 |
T939 |
amod |
post-natal,failure |
| R601 |
T941 |
T939 |
compound |
growth,failure |
| R602 |
T942 |
T939 |
cc |
and,failure |
| R603 |
T943 |
T944 |
amod |
primary,demyelination |
| R604 |
T944 |
T939 |
conj |
demyelination,failure |
| R605 |
T945 |
T944 |
acl |
resulting,demyelination |
| R606 |
T946 |
T945 |
prep |
in,resulting |
| R607 |
T947 |
T948 |
amod |
severe,neurodysfunction |
| R608 |
T948 |
T946 |
pobj |
neurodysfunction,in |
| R609 |
T949 |
T924 |
punct |
", ",are |
| R610 |
T950 |
T951 |
cc |
but,without |
| R611 |
T951 |
T924 |
prep |
without,are |
| R612 |
T952 |
T953 |
det |
a,predisposition |
| R613 |
T953 |
T951 |
pobj |
predisposition,without |
| R614 |
T954 |
T953 |
amod |
clear,predisposition |
| R615 |
T955 |
T953 |
compound |
cancer,predisposition |
| R616 |
T956 |
T957 |
punct |
[,12 |
| R617 |
T957 |
T924 |
parataxis |
12,are |
| R618 |
T958 |
T959 |
punct |
–,15 |
| R619 |
T959 |
T957 |
prep |
15,12 |
| R620 |
T960 |
T957 |
punct |
],12 |
| R621 |
T961 |
T924 |
punct |
.,are |
| R622 |
T963 |
T964 |
nsubj |
Patients,display |
| R623 |
T965 |
T963 |
prep |
with,Patients |
| R624 |
T966 |
T965 |
pobj |
TTD,with |
| R625 |
T967 |
T964 |
advmod |
additionally,display |
| R626 |
T968 |
T969 |
nmod |
hallmark,hair |
| R627 |
T969 |
T964 |
dobj |
hair,display |
| R628 |
T970 |
T971 |
npadvmod |
sulphur,deficient |
| R629 |
T971 |
T969 |
amod |
deficient,hair |
| R630 |
T972 |
T971 |
punct |
-,deficient |
| R631 |
T973 |
T969 |
amod |
brittle,hair |
| R632 |
T974 |
T969 |
cc |
and,hair |
| R633 |
T975 |
T969 |
conj |
nails,hair |
| R634 |
T976 |
T969 |
cc |
and,hair |
| R635 |
T977 |
T978 |
amod |
scaling,skin |
| R636 |
T978 |
T969 |
conj |
skin,hair |
| R637 |
T979 |
T980 |
punct |
[,13 |
| R638 |
T980 |
T969 |
parataxis |
13,hair |
| R639 |
T981 |
T980 |
punct |
],13 |
| R640 |
T982 |
T969 |
punct |
", ",hair |
| R641 |
T983 |
T969 |
acl |
resulting,hair |
| R642 |
T984 |
T983 |
prep |
from,resulting |
| R643 |
T985 |
T986 |
det |
a,defect |
| R644 |
T986 |
T984 |
pobj |
defect,from |
| R645 |
T987 |
T986 |
amod |
basal,defect |
| R646 |
T988 |
T986 |
compound |
transcription,defect |
| R647 |
T989 |
T986 |
prep |
in,defect |
| R648 |
T990 |
T991 |
amod |
specific,types |
| R649 |
T991 |
T989 |
pobj |
types,in |
| R650 |
T992 |
T991 |
compound |
cell,types |
| R651 |
T993 |
T994 |
punct |
[,17 |
| R652 |
T994 |
T964 |
parataxis |
17,display |
| R653 |
T995 |
T994 |
nummod |
16,17 |
| R654 |
T996 |
T994 |
punct |
",",17 |
| R655 |
T997 |
T994 |
punct |
],17 |
| R656 |
T998 |
T964 |
punct |
.,display |
| R657 |
T1000 |
T1001 |
det |
A,disorder |
| R658 |
T1001 |
T1003 |
nsubjpass |
disorder,described |
| R659 |
T1002 |
T1001 |
amod |
related,disorder |
| R660 |
T1004 |
T1001 |
prep |
with,disorder |
| R661 |
T1005 |
T1006 |
det |
the,predisposition |
| R662 |
T1006 |
T1004 |
pobj |
predisposition,with |
| R663 |
T1007 |
T1006 |
compound |
cancer,predisposition |
| R664 |
T1008 |
T1006 |
prep |
of,predisposition |
| R665 |
T1009 |
T1008 |
pobj |
XP,of |
| R666 |
T1010 |
T1006 |
acl |
combined,predisposition |
| R667 |
T1011 |
T1010 |
prep |
with,combined |
| R668 |
T1012 |
T1013 |
det |
the,complications |
| R669 |
T1013 |
T1011 |
pobj |
complications,with |
| R670 |
T1014 |
T1013 |
amod |
neurodevelopmental,complications |
| R671 |
T1015 |
T1013 |
prep |
of,complications |
| R672 |
T1016 |
T1015 |
pobj |
CS,of |
| R673 |
T1017 |
T1018 |
punct |
(,XPCS |
| R674 |
T1018 |
T1016 |
parataxis |
XPCS,CS |
| R675 |
T1019 |
T1018 |
punct |
),XPCS |
| R676 |
T1020 |
T1003 |
punct |
", ",described |
| R677 |
T1021 |
T1022 |
mark |
although,rare |
| R678 |
T1022 |
T1003 |
advcl |
rare,described |
| R679 |
T1023 |
T1003 |
punct |
", ",described |
| R680 |
T1024 |
T1003 |
aux |
has,described |
| R681 |
T1025 |
T1003 |
advmod |
also,described |
| R682 |
T1026 |
T1003 |
auxpass |
been,described |
| R683 |
T1027 |
T1028 |
punct |
[,18 |
| R684 |
T1028 |
T1003 |
parataxis |
18,described |
| R685 |
T1029 |
T1028 |
punct |
],18 |
| R686 |
T1030 |
T1003 |
punct |
.,described |
