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PMC:549712 / 29775-31061 JSONTXT

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craft-sa-dev

Id Subject Object Predicate Lexical cue
T9804 0-2 IN denotes In
T9805 23-32 VBN denotes generated
T9806 3-7 DT denotes this
T9807 8-13 NN denotes study
T9808 13-15 , denotes ,
T9809 15-17 PRP denotes we
T9810 18-22 VBP denotes have
T9811 33-34 DT denotes a
T9812 40-48 NN denotes mutation
T9813 35-39 JJ denotes null
T9814 49-51 IN denotes in
T9815 52-55 DT denotes the
T9816 92-96 NN denotes gene
T9817 56-74 NN denotes phosphatidylserine
T9818 75-83 NN denotes receptor
T9819 84-85 -LRB- denotes (
T9820 85-90 NN denotes Ptdsr
T9821 90-91 -RRB- denotes )
T9822 97-99 IN denotes in
T9823 100-105 NN denotes C57BL
T9824 106-108 NN denotes 6J
T9825 105-106 HYPH denotes /
T9826 109-113 NNS denotes mice
T9827 113-114 . denotes .
T9828 114-277 sentence denotes We show that ablation of Ptdsr results in profound differentiation defects in multiple organs and tissues during embryogenesis, although with variable penetrance.
T9829 115-117 PRP denotes We
T9830 118-122 VBP denotes show
T9831 123-127 IN denotes that
T9832 146-153 VBZ denotes results
T9833 128-136 NN denotes ablation
T9834 137-139 IN denotes of
T9835 140-145 NN denotes Ptdsr
T9836 154-156 IN denotes in
T9837 157-165 JJ denotes profound
T9838 182-189 NNS denotes defects
T9839 166-181 NN denotes differentiation
T9840 190-192 IN denotes in
T9841 193-201 JJ denotes multiple
T9842 202-208 NNS denotes organs
T9843 209-212 CC denotes and
T9844 213-220 NNS denotes tissues
T9845 221-227 IN denotes during
T9846 228-241 NN denotes embryogenesis
T9847 241-243 , denotes ,
T9848 243-251 IN denotes although
T9849 252-256 IN denotes with
T9850 257-265 JJ denotes variable
T9851 266-276 NN denotes penetrance
T9852 276-277 . denotes .
T9853 277-384 sentence denotes While this work was in progress, two other groups reported the generation of Ptdsr-deficient mice [31,32].
T9854 278-283 IN denotes While
T9855 294-297 VBD denotes was
T9856 284-288 DT denotes this
T9857 289-293 NN denotes work
T9858 328-336 VBD denotes reported
T9859 298-300 IN denotes in
T9860 301-309 NN denotes progress
T9861 309-311 , denotes ,
T9862 311-314 CD denotes two
T9863 321-327 NNS denotes groups
T9864 315-320 JJ denotes other
T9865 337-340 DT denotes the
T9866 341-351 NN denotes generation
T9867 352-354 IN denotes of
T9868 355-360 NN denotes Ptdsr
T9869 361-370 JJ denotes deficient
T9870 360-361 HYPH denotes -
T9871 371-375 NNS denotes mice
T9872 376-377 -LRB- denotes [
T9873 380-382 CD denotes 32
T9874 377-379 CD denotes 31
T9875 379-380 , denotes ,
T9876 382-383 -RRB- denotes ]
T9877 383-384 . denotes .
T9878 384-552 sentence denotes In all three knockout mouse lines, the first two exons ([31] and this study) or exons one to three [32] were deleted by replacement with a neomycin-selection cassette.
T9879 385-387 IN denotes In
T9880 494-501 VBN denotes deleted
T9881 388-391 DT denotes all
T9882 413-418 NNS denotes lines
T9883 392-397 CD denotes three
T9884 398-406 NN denotes knockout
T9885 407-412 NN denotes mouse
T9886 418-420 , denotes ,
T9887 420-423 DT denotes the
T9888 434-439 NNS denotes exons
T9889 424-429 JJ denotes first
T9890 430-433 CD denotes two
T9891 440-441 -LRB- denotes (
T9892 442-444 CD denotes 31
T9893 441-442 -LRB- denotes [
T9894 444-445 -RRB- denotes ]
T9895 446-449 CC denotes and
T9896 450-454 DT denotes this
T9897 455-460 NN denotes study
T9898 460-461 -RRB- denotes )
T9899 462-464 CC denotes or
T9900 465-470 NNS denotes exons
T9901 471-474 CD denotes one
T9902 475-477 IN denotes to
T9903 478-483 CD denotes three
T9904 484-485 -LRB- denotes [
T9905 485-487 CD denotes 32
T9906 487-488 -RRB- denotes ]
T9907 489-493 VBD denotes were
T9908 502-504 IN denotes by
T9909 505-516 NN denotes replacement
T9910 517-521 IN denotes with
T9911 522-523 DT denotes a
T9912 543-551 NN denotes cassette
T9913 524-532 NN denotes neomycin
T9914 533-542 NN denotes selection
T9915 532-533 HYPH denotes -
T9916 551-552 . denotes .
T9917 552-677 sentence denotes The Ptdsr-knockout mouse lines differ in the genetic background in which the mutation was generated and maintained, however.
T9918 553-556 DT denotes The
T9919 578-583 NNS denotes lines
T9920 557-562 NN denotes Ptdsr
T9921 572-577 NN denotes mouse
T9922 562-563 HYPH denotes -
T9923 563-571 NN denotes knockout
T9924 584-590 VBP denotes differ
T9925 591-593 IN denotes in
T9926 594-597 DT denotes the
T9927 606-616 NN denotes background
T9928 598-605 JJ denotes genetic
T9929 617-619 IN denotes in
T9930 643-652 VBN denotes generated
T9931 620-625 WDT denotes which
T9932 626-629 DT denotes the
T9933 630-638 NN denotes mutation
T9934 639-642 VBD denotes was
T9935 653-656 CC denotes and
T9936 657-667 VBN denotes maintained
T9937 667-669 , denotes ,
T9938 669-676 RB denotes however
T9939 676-677 . denotes .
T9940 677-903 sentence denotes In our case, the Ptdsr-null allele was generated in an isogenic C57BL/6J background, whereas Li et al. [31] and Kunisaki et al. [32] investigated the phenotype of their Ptdsr-knockout mice in a mixed 129 × C57BL/6 background.
T9941 678-680 IN denotes In
T9942 717-726 VBN denotes generated
T9943 681-684 PRP$ denotes our
T9944 685-689 NN denotes case
T9945 689-691 , denotes ,
T9946 691-694 DT denotes the
T9947 706-712 NN denotes allele
T9948 695-700 NN denotes Ptdsr
T9949 701-705 JJ denotes null
T9950 700-701 HYPH denotes -
T9951 713-716 VBD denotes was
T9952 727-729 IN denotes in
T9953 730-732 DT denotes an
T9954 751-761 NN denotes background
T9955 733-741 JJ denotes isogenic
T9956 742-747 NN denotes C57BL
T9957 748-750 NN denotes 6J
T9958 747-748 HYPH denotes /
T9959 761-763 , denotes ,
T9960 763-770 IN denotes whereas
T9961 811-823 VBD denotes investigated
T9962 771-773 NNP denotes Li
T9963 774-776 FW denotes et
T9964 777-780 FW denotes al.
T9965 781-782 -LRB- denotes [
T9966 782-784 CD denotes 31
T9967 784-785 -RRB- denotes ]
T9968 786-789 CC denotes and
T9969 790-798 NNP denotes Kunisaki
T9970 799-801 FW denotes et
T9971 802-805 FW denotes al.
T9972 806-807 -LRB- denotes [
T9973 807-809 CD denotes 32
T9974 809-810 -RRB- denotes ]
T9975 824-827 DT denotes the
T9976 828-837 NN denotes phenotype
T9977 838-840 IN denotes of
T9978 841-846 PRP$ denotes their
T9979 862-866 NNS denotes mice
T9980 847-852 NN denotes Ptdsr
T9981 853-861 NN denotes knockout
T9982 852-853 HYPH denotes -
T9983 867-869 IN denotes in
T9984 870-871 DT denotes a
T9985 892-902 NN denotes background
T9986 872-877 VBN denotes mixed
T9987 878-881 CD denotes 129
T9988 882-883 SYM denotes ×
T9989 884-889 NN denotes C57BL
T9990 889-890 HYPH denotes /
T9991 890-891 CD denotes 6
T9992 902-903 . denotes .
T9993 903-1110 sentence denotes The ablation of Ptdsr function results in perinatal lethality in all cases, but there are interesting differences in severity or expressivities of phenotypes among the different Ptdsr-deficient mouse lines.
T9994 904-907 DT denotes The
T9995 908-916 NN denotes ablation
T9996 935-942 VBZ denotes results
T9997 917-919 IN denotes of
T9998 920-925 NN denotes Ptdsr
T9999 926-934 NN denotes function
T10000 943-945 IN denotes in
T10001 946-955 JJ denotes perinatal
T10002 956-965 NN denotes lethality
T10003 966-968 IN denotes in
T10004 969-972 DT denotes all
T10005 973-978 NNS denotes cases
T10006 978-980 , denotes ,
T10007 980-983 CC denotes but
T10008 984-989 EX denotes there
T10009 990-993 VBP denotes are
T10010 994-1005 JJ denotes interesting
T10011 1006-1017 NNS denotes differences
T10012 1018-1020 IN denotes in
T10013 1021-1029 NN denotes severity
T10014 1030-1032 CC denotes or
T10015 1033-1047 NNS denotes expressivities
T10016 1048-1050 IN denotes of
T10017 1051-1061 NNS denotes phenotypes
T10018 1062-1067 IN denotes among
T10019 1068-1071 DT denotes the
T10020 1104-1109 NNS denotes lines
T10021 1072-1081 JJ denotes different
T10022 1082-1087 NN denotes Ptdsr
T10023 1088-1097 JJ denotes deficient
T10024 1087-1088 HYPH denotes -
T10025 1098-1103 NN denotes mouse
T10026 1109-1110 . denotes .
T10027 1110-1286 sentence denotes This might be due either to differences in genetic background or because the phenotypes that have been investigated in this study have not been analyzed in such detail before.
T10028 1111-1115 DT denotes This
T10029 1122-1124 VB denotes be
T10030 1116-1121 MD denotes might
T10031 1125-1128 IN denotes due
T10032 1129-1135 CC denotes either
T10033 1136-1138 IN denotes to
T10034 1139-1150 NNS denotes differences
T10035 1151-1153 IN denotes in
T10036 1154-1161 JJ denotes genetic
T10037 1162-1172 NN denotes background
T10038 1173-1175 CC denotes or
T10039 1176-1183 IN denotes because
T10040 1255-1263 VBN denotes analyzed
T10041 1184-1187 DT denotes the
T10042 1188-1198 NNS denotes phenotypes
T10043 1199-1203 WDT denotes that
T10044 1214-1226 VBN denotes investigated
T10045 1204-1208 VBP denotes have
T10046 1209-1213 VBN denotes been
T10047 1227-1229 IN denotes in
T10048 1230-1234 DT denotes this
T10049 1235-1240 NN denotes study
T10050 1241-1245 VBP denotes have
T10051 1246-1249 RB denotes not
T10052 1250-1254 VBN denotes been
T10053 1264-1266 IN denotes in
T10054 1267-1271 JJ denotes such
T10055 1272-1278 NN denotes detail
T10056 1279-1285 RB denotes before
T10057 1285-1286 . denotes .
R5303 T9804 T9805 prep In,generated
R5304 T9806 T9807 det this,study
R5305 T9807 T9804 pobj study,In
R5306 T9808 T9805 punct ", ",generated
R5307 T9809 T9805 nsubj we,generated
R5308 T9810 T9805 aux have,generated
R5309 T9811 T9812 det a,mutation
R5310 T9812 T9805 dobj mutation,generated
R5311 T9813 T9812 amod null,mutation
R5312 T9814 T9812 prep in,mutation
R5313 T9815 T9816 det the,gene
R5314 T9816 T9814 pobj gene,in
R5315 T9817 T9816 nmod phosphatidylserine,gene
R5316 T9818 T9816 nmod receptor,gene
R5317 T9819 T9820 punct (,Ptdsr
R5318 T9820 T9816 parataxis Ptdsr,gene
R5319 T9821 T9820 punct ),Ptdsr
R5320 T9822 T9812 prep in,mutation
R5321 T9823 T9824 compound C57BL,6J
R5322 T9824 T9826 compound 6J,mice
R5323 T9825 T9824 punct /,6J
R5324 T9826 T9822 pobj mice,in
R5325 T9827 T9805 punct .,generated
R5326 T9829 T9830 nsubj We,show
R5327 T9831 T9832 mark that,results
R5328 T9832 T9830 ccomp results,show
R5329 T9833 T9832 nsubj ablation,results
R5330 T9834 T9833 prep of,ablation
R5331 T9835 T9834 pobj Ptdsr,of
R5332 T9836 T9832 prep in,results
R5333 T9837 T9838 amod profound,defects
R5334 T9838 T9836 pobj defects,in
R5335 T9839 T9838 compound differentiation,defects
R5336 T9840 T9832 prep in,results
R5337 T9841 T9842 amod multiple,organs
R5338 T9842 T9840 pobj organs,in
R5339 T9843 T9842 cc and,organs
R5340 T9844 T9842 conj tissues,organs
R5341 T9845 T9832 prep during,results
R5342 T9846 T9845 pobj embryogenesis,during
R5343 T9847 T9832 punct ", ",results
R5344 T9848 T9849 mark although,with
R5345 T9849 T9832 advcl with,results
R5346 T9850 T9851 amod variable,penetrance
R5347 T9851 T9849 pobj penetrance,with
R5348 T9852 T9830 punct .,show
R5349 T9854 T9855 mark While,was
R5350 T9855 T9858 advcl was,reported
R5351 T9856 T9857 det this,work
R5352 T9857 T9855 nsubj work,was
R5353 T9859 T9855 prep in,was
R5354 T9860 T9859 pobj progress,in
R5355 T9861 T9858 punct ", ",reported
R5356 T9862 T9863 nummod two,groups
R5357 T9863 T9858 nsubj groups,reported
R5358 T9864 T9863 amod other,groups
R5359 T9865 T9866 det the,generation
R5360 T9866 T9858 dobj generation,reported
R5361 T9867 T9866 prep of,generation
R5362 T9868 T9869 npadvmod Ptdsr,deficient
R5363 T9869 T9871 amod deficient,mice
R5364 T9870 T9869 punct -,deficient
R5365 T9871 T9867 pobj mice,of
R5366 T9872 T9873 punct [,32
R5367 T9873 T9858 parataxis 32,reported
R5368 T9874 T9873 nummod 31,32
R5369 T9875 T9873 punct ",",32
R5370 T9876 T9873 punct ],32
R5371 T9877 T9858 punct .,reported
R5372 T9879 T9880 prep In,deleted
R5373 T9881 T9882 det all,lines
R5374 T9882 T9879 pobj lines,In
R5375 T9883 T9882 nummod three,lines
R5376 T9884 T9885 compound knockout,mouse
R5377 T9885 T9882 compound mouse,lines
R5378 T9886 T9880 punct ", ",deleted
R5379 T9887 T9888 det the,exons
R5380 T9888 T9880 nsubjpass exons,deleted
R5381 T9889 T9888 amod first,exons
R5382 T9890 T9888 nummod two,exons
R5383 T9891 T9892 punct (,31
R5384 T9892 T9888 parataxis 31,exons
R5385 T9893 T9892 punct [,31
R5386 T9894 T9892 punct ],31
R5387 T9895 T9892 cc and,31
R5388 T9896 T9897 det this,study
R5389 T9897 T9892 conj study,31
R5390 T9898 T9892 punct ),31
R5391 T9899 T9888 cc or,exons
R5392 T9900 T9901 nmod exons,one
R5393 T9901 T9888 conj one,exons
R5394 T9902 T9901 prep to,one
R5395 T9903 T9902 pobj three,to
R5396 T9904 T9905 punct [,32
R5397 T9905 T9901 parataxis 32,one
R5398 T9906 T9905 punct ],32
R5399 T9907 T9880 auxpass were,deleted
R5400 T9908 T9880 prep by,deleted
R5401 T9909 T9908 pobj replacement,by
R5402 T9910 T9909 prep with,replacement
R5403 T9911 T9912 det a,cassette
R5404 T9912 T9910 pobj cassette,with
R5405 T9913 T9914 compound neomycin,selection
R5406 T9914 T9912 compound selection,cassette
R5407 T9915 T9914 punct -,selection
R5408 T9916 T9880 punct .,deleted
R5409 T9918 T9919 det The,lines
R5410 T9919 T9924 nsubj lines,differ
R5411 T9920 T9921 compound Ptdsr,mouse
R5412 T9921 T9919 compound mouse,lines
R5413 T9922 T9921 punct -,mouse
R5414 T9923 T9921 compound knockout,mouse
R5415 T9925 T9924 prep in,differ
R5416 T9926 T9927 det the,background
R5417 T9927 T9925 pobj background,in
R5418 T9928 T9927 amod genetic,background
R5419 T9929 T9930 prep in,generated
R5420 T9930 T9927 relcl generated,background
R5421 T9931 T9929 pobj which,in
R5422 T9932 T9933 det the,mutation
R5423 T9933 T9930 nsubjpass mutation,generated
R5424 T9934 T9930 auxpass was,generated
R5425 T9935 T9930 cc and,generated
R5426 T9936 T9930 conj maintained,generated
R5427 T9937 T9924 punct ", ",differ
R5428 T9938 T9924 advmod however,differ
R5429 T9939 T9924 punct .,differ
R5430 T9941 T9942 prep In,generated
R5431 T9943 T9944 poss our,case
R5432 T9944 T9941 pobj case,In
R5433 T9945 T9942 punct ", ",generated
R5434 T9946 T9947 det the,allele
R5435 T9947 T9942 nsubjpass allele,generated
R5436 T9948 T9949 npadvmod Ptdsr,null
R5437 T9949 T9947 amod null,allele
R5438 T9950 T9949 punct -,null
R5439 T9951 T9942 auxpass was,generated
R5440 T9952 T9942 prep in,generated
R5441 T9953 T9954 det an,background
R5442 T9954 T9952 pobj background,in
R5443 T9955 T9954 amod isogenic,background
R5444 T9956 T9957 compound C57BL,6J
R5445 T9957 T9954 compound 6J,background
R5446 T9958 T9957 punct /,6J
R5447 T9959 T9942 punct ", ",generated
R5448 T9960 T9961 mark whereas,investigated
R5449 T9961 T9942 advcl investigated,generated
R5450 T9962 T9961 nsubj Li,investigated
R5451 T9963 T9964 advmod et,al.
R5452 T9964 T9962 advmod al.,Li
R5453 T9965 T9966 punct [,31
R5454 T9966 T9962 parataxis 31,Li
R5455 T9967 T9966 punct ],31
R5456 T9968 T9962 cc and,Li
R5457 T9969 T9962 conj Kunisaki,Li
R5458 T9970 T9971 advmod et,al.
R5459 T9971 T9969 advmod al.,Kunisaki
R5460 T9972 T9973 punct [,32
R5461 T9973 T9969 parataxis 32,Kunisaki
R5462 T9974 T9973 punct ],32
R5463 T9975 T9976 det the,phenotype
R5464 T9976 T9961 dobj phenotype,investigated
R5465 T9977 T9976 prep of,phenotype
R5466 T9978 T9979 poss their,mice
R5467 T9979 T9977 pobj mice,of
R5468 T9980 T9981 compound Ptdsr,knockout
R5469 T9981 T9979 compound knockout,mice
R5470 T9982 T9981 punct -,knockout
R5471 T9983 T9961 prep in,investigated
R5472 T9984 T9985 det a,background
R5473 T9985 T9983 pobj background,in
R5474 T9986 T9985 amod mixed,background
R5475 T9987 T9985 nummod 129,background
R5476 T9988 T9989 punct ×,C57BL
R5477 T9989 T9987 prep C57BL,129
R5478 T9990 T9989 punct /,C57BL
R5479 T9991 T9989 nummod 6,C57BL
R5480 T9992 T9942 punct .,generated
R5481 T9994 T9995 det The,ablation
R5482 T9995 T9996 nsubj ablation,results
R5483 T9997 T9995 prep of,ablation
R5484 T9998 T9999 compound Ptdsr,function
R5485 T9999 T9997 pobj function,of
R5486 T10000 T9996 prep in,results
R5487 T10001 T10002 amod perinatal,lethality
R5488 T10002 T10000 pobj lethality,in
R5489 T10003 T9996 prep in,results
R5490 T10004 T10005 det all,cases
R5491 T10005 T10003 pobj cases,in
R5492 T10006 T9996 punct ", ",results
R5493 T10007 T9996 cc but,results
R5494 T10008 T10009 expl there,are
R5495 T10009 T9996 conj are,results
R5496 T10010 T10011 amod interesting,differences
R5497 T10011 T10009 attr differences,are
R5498 T10012 T10011 prep in,differences
R5499 T10013 T10012 pobj severity,in
R5500 T10014 T10013 cc or,severity
R5501 T10015 T10013 conj expressivities,severity
R5502 T10016 T10013 prep of,severity
R5503 T10017 T10016 pobj phenotypes,of
R5504 T10018 T10011 prep among,differences
R5505 T10019 T10020 det the,lines
R5506 T10020 T10018 pobj lines,among
R5507 T10021 T10020 amod different,lines
R5508 T10022 T10023 npadvmod Ptdsr,deficient
R5509 T10023 T10020 amod deficient,lines
R5510 T10024 T10023 punct -,deficient
R5511 T10025 T10020 compound mouse,lines
R5512 T10026 T10009 punct .,are
R5513 T10028 T10029 nsubj This,be
R5514 T10030 T10029 aux might,be
R5515 T10031 T10029 prep due,be
R5516 T10032 T10031 preconj either,due
R5517 T10033 T10031 conj to,due
R5518 T10034 T10033 pobj differences,to
R5519 T10035 T10034 prep in,differences
R5520 T10036 T10037 amod genetic,background
R5521 T10037 T10035 pobj background,in
R5522 T10038 T10031 cc or,due
R5523 T10039 T10040 mark because,analyzed
R5524 T10040 T10031 conj analyzed,due
R5525 T10041 T10042 det the,phenotypes
R5526 T10042 T10040 nsubjpass phenotypes,analyzed
R5527 T10043 T10044 dep that,investigated
R5528 T10044 T10042 relcl investigated,phenotypes
R5529 T10045 T10044 aux have,investigated
R5530 T10046 T10044 auxpass been,investigated
R5531 T10047 T10044 prep in,investigated
R5532 T10048 T10049 det this,study
R5533 T10049 T10047 pobj study,in
R5534 T10050 T10040 aux have,analyzed
R5535 T10051 T10040 neg not,analyzed
R5536 T10052 T10040 auxpass been,analyzed
R5537 T10053 T10040 prep in,analyzed
R5538 T10054 T10055 amod such,detail
R5539 T10055 T10053 pobj detail,in
R5540 T10056 T10040 advmod before,analyzed
R5541 T10057 T10029 punct .,be

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
T9419 35-39 SO_EXT:sequence_nullness denotes null
T9420 40-48 SO_EXT:sequence_alteration_entity_or_process denotes mutation
T9421 56-74 CHEBI:18303 denotes phosphatidylserine
T9422 56-83 PR_EXT:000009218 denotes phosphatidylserine receptor
T9423 75-83 GO_EXT:0004872 denotes receptor
T9424 85-90 PR_EXT:000009218 denotes Ptdsr
T9425 92-96 SO_EXT:0000704 denotes gene
T9426 109-113 NCBITaxon:10088 denotes mice
T9427 140-145 PR_EXT:000009218 denotes Ptdsr
T9428 166-181 GO_RO_EXT:developmental_differentiation_process denotes differentiation
T9429 202-208 UBERON:0000062 denotes organs
T9430 213-220 UBERON:0000479 denotes tissues
T9431 228-241 GO:0009790 denotes embryogenesis
T9432 355-360 PR_EXT:000009218 denotes Ptdsr
T9433 371-375 NCBITaxon:10088 denotes mice
T9434 407-412 NCBITaxon:10088 denotes mouse
T9435 434-439 SO_EXT:0000147 denotes exons
T9436 465-470 SO_EXT:0000147 denotes exons
T9437 494-501 SO_EXT:sequence_deletion_process denotes deleted
T9438 505-516 SO_EXT:sequence_substitution_entity_or_process denotes replacement
T9439 524-532 CHEBI:7507 denotes neomycin
T9440 543-551 SO_EXT:0005853 denotes cassette
T9441 557-562 PR_EXT:000009218 denotes Ptdsr
T9442 572-577 NCBITaxon:10088 denotes mouse
T9443 598-605 SO_EXT:0000704 denotes genetic
T9444 630-638 SO_EXT:sequence_alteration_entity_or_process denotes mutation
T9445 695-700 PR_EXT:000009218 denotes Ptdsr
T9446 701-705 SO_EXT:sequence_nullness denotes null
T9447 706-712 SO_EXT:0001023 denotes allele
T9448 847-852 PR_EXT:000009218 denotes Ptdsr
T9449 862-866 NCBITaxon:10088 denotes mice
T9450 920-925 PR_EXT:000009218 denotes Ptdsr
T9451 946-955 UBERON:0012101 denotes perinatal
T9452 950-955 GO:0007567 denotes natal
T9453 956-965 GO_EXT:fatality_or_lethality denotes lethality
T9454 1082-1087 PR_EXT:000009218 denotes Ptdsr
T9455 1098-1103 NCBITaxon:10088 denotes mouse
T9456 1154-1161 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
T9133 56-74 CHEBI:18303 denotes phosphatidylserine
T9134 56-83 PR:000009218 denotes phosphatidylserine receptor
T9135 85-90 PR:000009218 denotes Ptdsr
T9136 92-96 SO:0000704 denotes gene
T9137 109-113 NCBITaxon:10088 denotes mice
T9138 140-145 PR:000009218 denotes Ptdsr
T9139 202-208 UBERON:0000062 denotes organs
T9140 213-220 UBERON:0000479 denotes tissues
T9141 228-241 GO:0009790 denotes embryogenesis
T9142 355-360 PR:000009218 denotes Ptdsr
T9143 371-375 NCBITaxon:10088 denotes mice
T9144 407-412 NCBITaxon:10088 denotes mouse
T9145 434-439 SO:0000147 denotes exons
T9146 465-470 SO:0000147 denotes exons
T9147 524-532 CHEBI:7507 denotes neomycin
T9148 543-551 SO:0005853 denotes cassette
T9149 557-562 PR:000009218 denotes Ptdsr
T9150 572-577 NCBITaxon:10088 denotes mouse
T9151 598-605 SO:0000704 denotes genetic
T9152 695-700 PR:000009218 denotes Ptdsr
T9153 706-712 SO:0001023 denotes allele
T9154 847-852 PR:000009218 denotes Ptdsr
T9155 862-866 NCBITaxon:10088 denotes mice
T9156 920-925 PR:000009218 denotes Ptdsr
T9157 946-955 UBERON:0012101 denotes perinatal
T9158 950-955 GO:0007567 denotes natal
T9159 1082-1087 PR:000009218 denotes Ptdsr
T9160 1098-1103 NCBITaxon:10088 denotes mouse
T9161 1154-1161 SO:0000704 denotes genetic

2_test

Id Subject Object Predicate Lexical cue
15345036-14645847-55938512 377-379 14645847 denotes 31
15345036-14715629-55938513 380-382 14715629 denotes 32
15345036-14645847-55938514 442-444 14645847 denotes 31
15345036-14715629-55938515 485-487 14715629 denotes 32
15345036-14645847-55938516 782-784 14645847 denotes 31
15345036-14715629-55938517 807-809 14715629 denotes 32