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PMC:1183529 / 4902-5771 JSONTXT

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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
T2455 88-101 UBERON:0001103 denotes diaphragmatic
T2456 114-123 UBERON:0002048 denotes pulmonary
T2457 138-144 NCBITaxon:9606 denotes humans
T2458 297-304 SO:0000704 denotes genetic
T2459 455-468 UBERON:0001103 denotes diaphragmatic
T2460 455-480 GO:0060539 denotes diaphragmatic development
T2461 672-678 NCBITaxon:9606 denotes humans
T2462 724-730 NCBITaxon:33208 denotes animal
T2463 741-746 NCBITaxon:9606 denotes human
T2464 747-752 GO:0007567 denotes birth
T2465 778-785 SO:0000704 denotes genetic
T2466 809-815 NCBITaxon:33208 denotes animal
T2467 851-856 NCBITaxon:9606 denotes human

2_test

Id Subject Object Predicate Lexical cue
16103912-12725592-85559732 593-595 12725592 denotes 12
16103912-9788565-85559733 596-598 9788565 denotes 13
T44365 593-595 12725592 denotes 12
T34234 596-598 9788565 denotes 13

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
T2523 37-46 SO_EXT:sequence_alteration_entity_or_process denotes mutations
T2524 88-101 UBERON:0001103 denotes diaphragmatic
T2525 114-123 UBERON:0002048 denotes pulmonary
T2526 138-144 NCBITaxon:9606 denotes humans
T2527 297-304 SO_EXT:0000704 denotes genetic
T2528 375-384 SO_EXT:sequence_alteration_entity_or_process denotes mutations
T2529 409-418 CHEBI_EXT:polyatomic_entity_or_group denotes molecular
T2530 455-468 UBERON:0001103 denotes diaphragmatic
T2531 455-480 GO:0060539 denotes diaphragmatic development
T2532 539-550 GO_SO_EXT:chromosome denotes chromosomal
T2533 634-640 GO_EXT:fatality_or_lethality denotes lethal
T2534 672-678 NCBITaxon:9606 denotes humans
T2535 724-730 NCBITaxon:33208 denotes animal
T2536 741-746 NCBITaxon:9606 denotes human
T2537 747-752 GO:0007567 denotes birth
T2538 778-785 SO_EXT:0000704 denotes genetic
T2539 809-815 NCBITaxon:33208 denotes animal
T2540 851-856 NCBITaxon:9606 denotes human

craft-sa-dev

Id Subject Object Predicate Lexical cue
T2899 0-2 IN denotes To
T2900 20-24 VBN denotes been
T2901 3-7 NN denotes date
T2902 7-9 , denotes ,
T2903 9-14 EX denotes there
T2904 15-19 VBP denotes have
T2905 25-27 DT denotes no
T2906 37-46 NNS denotes mutations
T2907 28-36 JJ denotes specific
T2908 47-52 VBN denotes found
T2909 53-55 TO denotes to
T2910 56-58 VB denotes be
T2911 59-69 JJ denotes associated
T2912 70-74 IN denotes with
T2913 75-87 JJ denotes nonsyndromic
T2914 102-109 NNS denotes defects
T2915 88-101 JJ denotes diaphragmatic
T2916 110-113 CC denotes and
T2917 114-123 JJ denotes pulmonary
T2918 124-134 NN denotes hypoplasia
T2919 135-137 IN denotes in
T2920 138-144 NNS denotes humans
T2921 144-145 . denotes .
T2922 145-292 sentence denotes The heritability of these defects is unclear, as the high morbidity and mortality limit the collection of multigenerational families for analysis.
T2923 146-149 DT denotes The
T2924 150-162 NN denotes heritability
T2925 180-182 VBZ denotes is
T2926 163-165 IN denotes of
T2927 166-171 DT denotes these
T2928 172-179 NNS denotes defects
T2929 183-190 JJ denotes unclear
T2930 190-192 , denotes ,
T2931 192-194 IN denotes as
T2932 228-233 VBP denotes limit
T2933 195-198 DT denotes the
T2934 204-213 NN denotes morbidity
T2935 199-203 JJ denotes high
T2936 214-217 CC denotes and
T2937 218-227 NN denotes mortality
T2938 234-237 DT denotes the
T2939 238-248 NN denotes collection
T2940 249-251 IN denotes of
T2941 252-269 JJ denotes multigenerational
T2942 270-278 NNS denotes families
T2943 279-282 IN denotes for
T2944 283-291 NN denotes analysis
T2945 291-292 . denotes .
T2946 292-481 sentence denotes The genetic etiologies are likely to be complex and probably arise from different mutations in various parts of the molecular developmental pathways required for diaphragmatic development.
T2947 293-296 DT denotes The
T2948 305-315 NNS denotes etiologies
T2949 297-304 JJ denotes genetic
T2950 316-319 VBP denotes are
T2951 320-326 JJ denotes likely
T2952 327-329 TO denotes to
T2953 330-332 VB denotes be
T2954 333-340 JJ denotes complex
T2955 341-344 CC denotes and
T2956 345-353 RB denotes probably
T2957 354-359 VBP denotes arise
T2958 360-364 IN denotes from
T2959 365-374 JJ denotes different
T2960 375-384 NNS denotes mutations
T2961 385-387 IN denotes in
T2962 388-395 JJ denotes various
T2963 396-401 NNS denotes parts
T2964 402-404 IN denotes of
T2965 405-408 DT denotes the
T2966 433-441 NNS denotes pathways
T2967 409-418 JJ denotes molecular
T2968 419-432 JJ denotes developmental
T2969 442-450 VBN denotes required
T2970 451-454 IN denotes for
T2971 455-468 JJ denotes diaphragmatic
T2972 469-480 NN denotes development
T2973 480-481 . denotes .
T2974 481-600 sentence denotes Indeed, there are numerous reports implicating different chromosomal abnormalities in the pathogenesis of CDH [12,13].
T2975 482-488 RB denotes Indeed
T2976 496-499 VBP denotes are
T2977 488-490 , denotes ,
T2978 490-495 EX denotes there
T2979 500-508 JJ denotes numerous
T2980 509-516 NNS denotes reports
T2981 517-528 VBG denotes implicating
T2982 529-538 JJ denotes different
T2983 551-564 NNS denotes abnormalities
T2984 539-550 JJ denotes chromosomal
T2985 565-567 IN denotes in
T2986 568-571 DT denotes the
T2987 572-584 NN denotes pathogenesis
T2988 585-587 IN denotes of
T2989 588-591 NN denotes CDH
T2990 592-593 -LRB- denotes [
T2991 596-598 CD denotes 13
T2992 593-595 CD denotes 12
T2993 595-596 , denotes ,
T2994 598-599 -RRB- denotes ]
T2995 599-600 . denotes .
T2996 600-869 sentence denotes Given the difficulty of studying lethal developmental abnormalities in humans, it is of great potential utility to develop animal models of human birth defects, as the specific genetic abnormalities found in animal models can then be investigated in human populations.
T2997 601-606 VBN denotes Given
T2998 683-685 VBZ denotes is
T2999 607-610 DT denotes the
T3000 611-621 NN denotes difficulty
T3001 622-624 IN denotes of
T3002 625-633 VBG denotes studying
T3003 634-640 JJ denotes lethal
T3004 655-668 NNS denotes abnormalities
T3005 641-654 JJ denotes developmental
T3006 669-671 IN denotes in
T3007 672-678 NNS denotes humans
T3008 678-680 , denotes ,
T3009 680-682 PRP denotes it
T3010 686-688 IN denotes of
T3011 689-694 JJ denotes great
T3012 705-712 NN denotes utility
T3013 695-704 JJ denotes potential
T3014 713-715 TO denotes to
T3015 716-723 VB denotes develop
T3016 724-730 NN denotes animal
T3017 731-737 NNS denotes models
T3018 738-740 IN denotes of
T3019 741-746 JJ denotes human
T3020 753-760 NNS denotes defects
T3021 747-752 NN denotes birth
T3022 760-762 , denotes ,
T3023 762-764 IN denotes as
T3024 835-847 VBN denotes investigated
T3025 765-768 DT denotes the
T3026 786-799 NNS denotes abnormalities
T3027 769-777 JJ denotes specific
T3028 778-785 JJ denotes genetic
T3029 800-805 VBN denotes found
T3030 806-808 IN denotes in
T3031 809-815 NN denotes animal
T3032 816-822 NNS denotes models
T3033 823-826 MD denotes can
T3034 827-831 RB denotes then
T3035 832-834 VB denotes be
T3036 848-850 IN denotes in
T3037 851-856 JJ denotes human
T3038 857-868 NNS denotes populations
T3039 868-869 . denotes .
R538 T2899 T2900 prep To,been
R539 T2901 T2899 pobj date,To
R540 T2902 T2900 punct ", ",been
R541 T2903 T2900 expl there,been
R542 T2904 T2900 aux have,been
R543 T2905 T2906 det no,mutations
R544 T2906 T2900 attr mutations,been
R545 T2907 T2906 amod specific,mutations
R546 T2908 T2906 acl found,mutations
R547 T3015 T2998 xcomp develop,is
R548 T3016 T3017 compound animal,models
R549 T3017 T3015 dobj models,develop
R550 T3018 T3017 prep of,models
R551 T3019 T3020 amod human,defects
R552 T3020 T3018 pobj defects,of
R553 T3021 T3020 compound birth,defects
R554 T3022 T3015 punct ", ",develop
R555 T3023 T3024 mark as,investigated
R556 T3024 T3015 advcl investigated,develop
R557 T3025 T3026 det the,abnormalities
R558 T3026 T3024 nsubjpass abnormalities,investigated
R559 T2909 T2910 aux to,be
R560 T3027 T3026 amod specific,abnormalities
R561 T2910 T2908 xcomp be,found
R562 T3028 T3026 amod genetic,abnormalities
R563 T2911 T2910 acomp associated,be
R564 T2912 T2911 prep with,associated
R565 T3029 T3026 acl found,abnormalities
R566 T2913 T2914 amod nonsyndromic,defects
R567 T2914 T2912 pobj defects,with
R568 T2915 T2914 amod diaphragmatic,defects
R569 T3030 T3029 prep in,found
R570 T2916 T2914 cc and,defects
R571 T2917 T2918 amod pulmonary,hypoplasia
R572 T3031 T3032 compound animal,models
R573 T2918 T2914 conj hypoplasia,defects
R574 T2919 T2910 prep in,be
R575 T2920 T2919 pobj humans,in
R576 T3032 T3030 pobj models,in
R577 T2921 T2900 punct .,been
R578 T3033 T3024 aux can,investigated
R579 T2923 T2924 det The,heritability
R580 T2924 T2925 nsubj heritability,is
R581 T3034 T3024 advmod then,investigated
R582 T2926 T2924 prep of,heritability
R583 T2927 T2928 det these,defects
R584 T3035 T3024 auxpass be,investigated
R585 T2928 T2926 pobj defects,of
R586 T2929 T2925 acomp unclear,is
R587 T3036 T3024 prep in,investigated
R588 T3037 T3038 amod human,populations
R589 T2930 T2925 punct ", ",is
R590 T2931 T2932 mark as,limit
R591 T3038 T3036 pobj populations,in
R592 T2932 T2925 advcl limit,is
R593 T2933 T2934 det the,morbidity
R594 T3039 T2998 punct .,is
R595 T2934 T2932 nsubj morbidity,limit
R596 T2935 T2934 amod high,morbidity
R597 T2936 T2934 cc and,morbidity
R599 T2937 T2934 conj mortality,morbidity
R600 T2938 T2939 det the,collection
R601 T2939 T2932 dobj collection,limit
R602 T2940 T2939 prep of,collection
R604 T2941 T2942 amod multigenerational,families
R605 T2942 T2940 pobj families,of
R606 T2943 T2939 prep for,collection
R607 T2944 T2943 pobj analysis,for
R608 T2945 T2925 punct .,is
R610 T2947 T2948 det The,etiologies
R611 T2948 T2950 nsubj etiologies,are
R612 T2949 T2948 amod genetic,etiologies
R614 T2951 T2950 acomp likely,are
R615 T2952 T2953 aux to,be
R617 T2953 T2951 xcomp be,likely
R618 T2954 T2953 acomp complex,be
R620 T2955 T2950 cc and,are
R621 T2956 T2957 advmod probably,arise
R622 T2957 T2950 conj arise,are
R624 T2958 T2957 prep from,arise
R625 T2959 T2960 amod different,mutations
R626 T2960 T2958 pobj mutations,from
R628 T2961 T2957 prep in,arise
R629 T2962 T2963 amod various,parts
R630 T2963 T2961 pobj parts,in
R631 T2964 T2963 prep of,parts
R633 T2965 T2966 det the,pathways
R634 T2966 T2964 pobj pathways,of
R636 T2967 T2966 amod molecular,pathways
R637 T2968 T2966 amod developmental,pathways
R638 T2969 T2966 acl required,pathways
R640 T2970 T2969 prep for,required
R641 T2971 T2972 amod diaphragmatic,development
R642 T2972 T2970 pobj development,for
R644 T2973 T2950 punct .,are
R646 T2975 T2976 advmod Indeed,are
R648 T2977 T2976 punct ", ",are
R649 T2978 T2976 expl there,are
R650 T2979 T2980 amod numerous,reports
R652 T2980 T2976 attr reports,are
R653 T2981 T2980 acl implicating,reports
R654 T2982 T2983 amod different,abnormalities
R655 T2983 T2981 dobj abnormalities,implicating
R657 T2984 T2983 amod chromosomal,abnormalities
R658 T2985 T2981 prep in,implicating
R659 T2986 T2987 det the,pathogenesis
R660 T2987 T2985 pobj pathogenesis,in
R661 T2988 T2987 prep of,pathogenesis
R663 T2989 T2988 pobj CDH,of
R664 T2990 T2991 punct [,13
R665 T2991 T2976 parataxis 13,are
R667 T2992 T2991 nummod 12,13
R668 T2993 T2991 punct ",",13
R669 T2994 T2991 punct ],13
R671 T2995 T2976 punct .,are
R673 T2997 T2998 prep Given,is
R674 T2999 T3000 det the,difficulty
R676 T3000 T2997 pobj difficulty,Given
R677 T3001 T3000 prep of,difficulty
R678 T3002 T3001 pcomp studying,of
R680 T3003 T3004 amod lethal,abnormalities
R681 T3004 T3002 dobj abnormalities,studying
R683 T3005 T3004 amod developmental,abnormalities
R684 T3006 T3002 prep in,studying
R685 T3007 T3006 pobj humans,in
R687 T3008 T2998 punct ", ",is
R688 T3009 T2998 nsubj it,is
R689 T3010 T2998 prep of,is
R691 T3011 T3012 amod great,utility
R692 T3012 T3010 pobj utility,of
R694 T3013 T3012 amod potential,utility
R695 T3014 T3015 aux to,develop