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PMC:1892049 / 3882-4452 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
T6033 0-8 GO_EXT:breeding denotes Breeding
T6034 78-87 GO:0030849 denotes autosomal
T6035 170-176 SO_EXT:0001026 denotes genome
T6036 221-252 SO_EXT:0000694 denotes single nucleotide polymorphisms
T6037 228-238 CHEBI_SO_EXT:nucleotide denotes nucleotide
T6038 254-258 SO_EXT:0000694 denotes SNPs
T6039 283-288 NCBITaxon:10088 denotes mouse
T6040 289-295 SO_EXT:0001026 denotes genome
T6041 336-343 SO_EXT:0001026 denotes genomic
T6042 431-437 CHEBI_SO_EXT:molecular_indicator_or_label_or_marker_or_tag denotes marker
T6043 456-466 GO_SO_EXT:chromosome denotes Chromosome
T6044 484-493 SO_EXT:0001024 denotes haplotype
T6045 508-516 SO_EXT:sequence_alteration_entity_or_process denotes mutation

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
T5815 78-87 GO:0030849 denotes autosomal
T5816 170-176 SO:0001026 denotes genome
T5817 221-252 SO:0000694 denotes single nucleotide polymorphisms
T5818 254-258 SO:0000694 denotes SNPs
T5819 283-288 NCBITaxon:10088 denotes mouse
T5820 289-295 SO:0001026 denotes genome
T5821 336-343 SO:0001026 denotes genomic
T5822 484-493 SO:0001024 denotes haplotype

craft-sa-dev

Id Subject Object Predicate Lexical cue
T6543 289-295 NN denotes genome
T6544 283-288 NN denotes mouse
T6494 0-8 NN denotes Breeding
T6495 9-20 NNS denotes experiments
T6496 21-30 VBD denotes suggested
T6497 31-35 IN denotes that
T6498 62-71 VBN denotes inherited
T6499 36-39 DT denotes the
T6500 49-57 NN denotes disorder
T6501 40-48 VBN denotes observed
T6502 58-61 VBD denotes was
T6503 72-74 IN denotes in
T6504 75-77 DT denotes an
T6505 98-104 NN denotes manner
T6506 78-87 JJ denotes autosomal
T6507 88-97 JJ denotes recessive
T6508 104-105 . denotes .
T6509 105-296 sentence denotes To map the location of the disease-causing lesion, we performed genome-wide linkage analysis using strain-specific single nucleotide polymorphisms (SNPs) at 120 loci across the mouse genome.
T6510 106-108 TO denotes To
T6511 109-112 VB denotes map
T6512 160-169 VBD denotes performed
T6513 113-116 DT denotes the
T6514 117-125 NN denotes location
T6515 126-128 IN denotes of
T6516 129-132 DT denotes the
T6517 149-155 NN denotes lesion
T6518 133-140 NN denotes disease
T6519 141-148 VBG denotes causing
T6520 140-141 HYPH denotes -
T6521 155-157 , denotes ,
T6522 157-159 PRP denotes we
T6523 170-176 NN denotes genome
T6524 177-181 JJ denotes wide
T6525 176-177 HYPH denotes -
T6526 190-198 NN denotes analysis
T6527 182-189 NN denotes linkage
T6528 199-204 VBG denotes using
T6529 205-211 NN denotes strain
T6530 212-220 JJ denotes specific
T6531 211-212 HYPH denotes -
T6532 239-252 NNS denotes polymorphisms
T6533 221-227 JJ denotes single
T6534 228-238 NN denotes nucleotide
T6535 253-254 -LRB- denotes (
T6536 254-258 NNS denotes SNPs
T6537 258-259 -RRB- denotes )
T6538 260-262 IN denotes at
T6539 263-266 CD denotes 120
T6540 267-271 NNS denotes loci
T6541 272-278 IN denotes across
T6542 279-282 DT denotes the
T6545 295-296 . denotes .
T6546 296-472 sentence denotes Analysis of these data showed a single genomic region with significant linkage to disease, providing a two-point LOD score of 5.13 at marker 20.MMHAP85FLG2 on Chromosome 6qE1.
T6547 297-305 NN denotes Analysis
T6548 320-326 VBD denotes showed
T6549 306-308 IN denotes of
T6550 309-314 DT denotes these
T6551 315-319 NNS denotes data
T6552 327-328 DT denotes a
T6553 344-350 NN denotes region
T6554 329-335 JJ denotes single
T6555 336-343 JJ denotes genomic
T6556 351-355 IN denotes with
T6557 356-367 JJ denotes significant
T6558 368-375 NN denotes linkage
T6559 376-378 IN denotes to
T6560 379-386 NN denotes disease
T6561 386-388 , denotes ,
T6562 388-397 VBG denotes providing
T6563 398-399 DT denotes a
T6564 414-419 NN denotes score
T6565 400-403 CD denotes two
T6566 404-409 NN denotes point
T6567 403-404 HYPH denotes -
T6568 410-413 NN denotes LOD
T6569 420-422 IN denotes of
T6570 423-427 CD denotes 5.13
T6571 428-430 IN denotes at
T6572 431-437 NN denotes marker
T6573 438-452 NN denotes 20.MMHAP85FLG2
T6574 453-455 IN denotes on
T6575 456-466 NN denotes Chromosome
T6576 467-471 NN denotes 6qE1
T6577 471-472 . denotes .
T6578 472-570 sentence denotes The linked haplotype suggested the mutation had occurred on the 129x1/SvJ background (Figure S1).
T6579 473-476 DT denotes The
T6580 484-493 NN denotes haplotype
T6581 477-483 VBN denotes linked
T6582 494-503 VBD denotes suggested
T6583 504-507 DT denotes the
T6584 508-516 NN denotes mutation
T6585 521-529 VBN denotes occurred
T6586 517-520 VBD denotes had
T6587 530-532 IN denotes on
T6588 533-536 DT denotes the
T6589 547-557 NN denotes background
T6590 537-542 NN denotes 129x1
T6591 543-546 NN denotes SvJ
T6592 542-543 HYPH denotes /
T6593 558-559 -LRB- denotes (
T6594 566-568 NN denotes S1
T6595 559-565 NN denotes Figure
T6596 568-569 -RRB- denotes )
T6597 569-570 . denotes .
R476 T6494 T6495 compound Breeding,experiments
R480 T6495 T6496 nsubj experiments,suggested
R484 T6497 T6498 mark that,inherited
R488 T6498 T6496 ccomp inherited,suggested
R492 T6499 T6500 det the,disorder
R494 T6500 T6498 nsubjpass disorder,inherited
R498 T6501 T6500 amod observed,disorder
R504 T6502 T6498 auxpass was,inherited
R509 T6503 T6498 prep in,inherited
R513 T6504 T6505 det an,manner
R517 T6505 T6503 pobj manner,in
R521 T6506 T6505 amod autosomal,manner
R525 T6507 T6505 amod recessive,manner
R529 T6508 T6496 punct .,suggested
R532 T6510 T6511 aux To,map
R538 T6511 T6512 advcl map,performed
R541 T6513 T6514 det the,location
R545 T6514 T6511 dobj location,map
R546 T6515 T6514 prep of,location
R547 T6516 T6517 det the,lesion
R548 T6517 T6515 pobj lesion,of
R549 T6518 T6519 npadvmod disease,causing
R550 T6579 T6580 det The,haplotype
R551 T6519 T6517 amod causing,lesion
R552 T6580 T6582 nsubj haplotype,suggested
R553 T6581 T6580 amod linked,haplotype
R554 T6583 T6584 det the,mutation
R555 T6584 T6585 nsubj mutation,occurred
R556 T6520 T6519 punct -,causing
R557 T6585 T6582 advcl occurred,suggested
R558 T6586 T6585 aux had,occurred
R559 T6521 T6512 punct ", ",performed
R560 T6587 T6585 prep on,occurred
R561 T6588 T6589 det the,background
R562 T6522 T6512 nsubj we,performed
R563 T6589 T6587 pobj background,on
R564 T6523 T6524 npadvmod genome,wide
R565 T6590 T6591 compound 129x1,SvJ
R566 T6591 T6589 compound SvJ,background
R567 T6524 T6526 amod wide,analysis
R568 T6592 T6591 punct /,SvJ
R569 T6593 T6594 punct (,S1
R570 T6594 T6582 parataxis S1,suggested
R571 T6525 T6524 punct -,wide
R572 T6595 T6594 compound Figure,S1
R573 T6596 T6594 punct ),S1
R574 T6597 T6582 punct .,suggested
R575 T6526 T6512 dobj analysis,performed
R578 T6527 T6526 compound linkage,analysis
R580 T6528 T6512 advcl using,performed
R584 T6529 T6530 npadvmod strain,specific
R588 T6530 T6532 amod specific,polymorphisms
R591 T6531 T6530 punct -,specific
R595 T6532 T6528 dobj polymorphisms,using
R600 T6533 T6534 amod single,nucleotide
R603 T6534 T6532 compound nucleotide,polymorphisms
R608 T6535 T6532 punct (,polymorphisms
R613 T6536 T6532 appos SNPs,polymorphisms
R614 T6537 T6528 punct ),using
R619 T6538 T6528 prep at,using
R621 T6539 T6540 nummod 120,loci
R625 T6540 T6538 pobj loci,at
R630 T6541 T6528 prep across,using
R633 T6542 T6543 det the,genome
R637 T6543 T6541 pobj genome,across
R641 T6544 T6543 compound mouse,genome
R645 T6545 T6512 punct .,performed
R649 T6547 T6548 nsubj Analysis,showed
R654 T6549 T6547 prep of,Analysis
R664 T6550 T6551 det these,data
R668 T6551 T6549 pobj data,of
R671 T6552 T6553 det a,region
R673 T6553 T6548 dobj region,showed
R675 T6554 T6553 amod single,region
R678 T6555 T6553 amod genomic,region
R682 T6556 T6553 prep with,region
R684 T6557 T6558 amod significant,linkage
R685 T6558 T6556 pobj linkage,with
R687 T6559 T6558 prep to,linkage
R690 T6560 T6559 pobj disease,to
R693 T6561 T6548 punct ", ",showed
R696 T6562 T6548 advcl providing,showed
R700 T6563 T6564 det a,score
R704 T6564 T6562 dobj score,providing
R708 T6565 T6566 nummod two,point
R715 T6566 T6564 compound point,score
R719 T6567 T6566 punct -,point
R721 T6568 T6564 compound LOD,score
R726 T6569 T6564 prep of,score
R730 T6570 T6569 pobj 5.13,of
R733 T6571 T6564 prep at,score
R736 T6572 T6573 compound marker,20.MMHAP85FLG2
R740 T6573 T6571 pobj 20.MMHAP85FLG2,at
R743 T6574 T6573 prep on,20.MMHAP85FLG2
R748 T6575 T6576 compound Chromosome,6qE1
R751 T6576 T6574 pobj 6qE1,on
R756 T6577 T6548 punct .,showed