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PMC:1564426 / 3895-4111 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
T2260 9-18 SO_EXT:sequence_alteration_entity_or_process denotes mutations
T2261 22-25 PR_EXT:000004122 denotes APC
T2262 161-171 UBERON:0012652 denotes colorectal

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
T2111 22-25 PR:000004122 denotes APC
T2112 161-171 UBERON:0012652 denotes colorectal

craft-sa-dev

Id Subject Object Predicate Lexical cue
T2582 9-18 NNS denotes mutations
T2584 0-8 NN denotes germline
T2585 26-31 VBP denotes cause
T2586 19-21 IN denotes in
T2587 22-25 NN denotes APC
T2588 32-40 JJ denotes familial
T2589 53-61 NN denotes polypois
T2590 41-52 JJ denotes adenomatous
T2591 62-63 -LRB- denotes (
T2592 63-66 NN denotes FAP
T2593 66-67 -RRB- denotes )
T2594 68-71 CC denotes and
T2595 72-75 PRP$ denotes its
T2596 76-83 NN denotes variant
T2597 83-85 , denotes ,
T2598 85-92 NNP denotes Gardner
T2599 93-101 NN denotes syndrome
T2600 101-102 . denotes .
T2602 103-106 NN denotes FAP
T2603 107-115 NNS denotes patients
T2604 120-133 VBN denotes characterized
T2605 116-119 VBP denotes are
T2606 134-136 IN denotes by
T2607 137-145 NNS denotes hundreds
T2608 146-148 IN denotes of
T2609 149-160 JJ denotes adenomatous
T2610 172-178 NNS denotes polyps
T2611 161-171 JJ denotes colorectal
T2612 178-180 , denotes ,
T2613 180-184 IN denotes with
T2614 185-187 DT denotes an
T2616 188-194 RB denotes almost
T2617 195-205 JJ denotes inevitable
R435 T2605 T2604 auxpass are,characterized
R437 T2606 T2604 agent by,characterized
R438 T2607 T2606 pobj hundreds,by
R440 T2608 T2607 prep of,hundreds
R441 T2609 T2610 amod adenomatous,polyps
R442 T2610 T2608 pobj polyps,of
R443 T2611 T2610 amod colorectal,polyps
R444 T2612 T2610 punct ", ",polyps
R445 T2613 T2610 prep with,polyps
R449 T2616 T2617 advmod almost,inevitable
R506 T2582 T2585 nsubj mutations,cause
R514 T2584 T2582 compound germline,mutations
R518 T2586 T2582 prep in,mutations
R519 T2587 T2586 pobj APC,in
R522 T2588 T2589 amod familial,polypois
R526 T2589 T2585 dobj polypois,cause
R529 T2590 T2589 amod adenomatous,polypois
R533 T2591 T2589 punct (,polypois
R537 T2592 T2589 appos FAP,polypois
R541 T2593 T2589 punct ),polypois
R545 T2594 T2589 cc and,polypois
R552 T2595 T2596 poss its,variant
R556 T2596 T2589 conj variant,polypois
R560 T2597 T2596 punct ", ",variant
R565 T2598 T2599 compound Gardner,syndrome
R568 T2599 T2596 appos syndrome,variant
R570 T2600 T2585 punct .,cause
R571 T2602 T2603 compound FAP,patients
R572 T2603 T2604 nsubjpass patients,characterized