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PMC:1892049 / 4626-4827 JSONTXT 4 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue
T6628 0-201 sentence denotes The underlying genetic lesion causing the opt phenotype is a homozygous in-frame deletion of exons 43 and 44 of the gene Itpr1 (Itpr1opt /opt), encoding inositol 1,4,5-triphosphate receptor 1 (Itpr1).
T6629 1-4 DT denotes The
T6631 5-15 VBG denotes underlying
T6632 16-23 JJ denotes genetic
T6630 24-30 NN denotes lesion
T6634 31-38 VBG denotes causing
T6635 39-42 DT denotes the
T6637 43-46 NN denotes opt
T6636 47-56 NN denotes phenotype
T6633 57-59 VBZ denotes is
T6638 60-61 DT denotes a
T6640 62-72 JJ denotes homozygous
T6641 73-75 IN denotes in
T6643 75-76 HYPH denotes -
T6642 76-81 NN denotes frame
T6639 82-90 NN denotes deletion
T6644 91-93 IN denotes of
T6645 94-99 NNS denotes exons
T6646 100-102 CD denotes 43
T6647 103-106 CC denotes and
T6648 107-109 CD denotes 44
T6649 110-112 IN denotes of
T6650 113-116 DT denotes the
T6652 117-121 NN denotes gene
T6651 122-127 NN denotes Itpr1
T6653 128-129 -LRB- denotes (
T6655 129-137 NN denotes Itpr1opt
T6656 138-139 HYPH denotes /
T6654 139-142 NN denotes opt
T6657 142-143 -RRB- denotes )
T6658 143-145 , denotes ,
T6659 145-153 VBG denotes encoding
T6660 154-162 NN denotes inositol
T6662 163-164 CD denotes 1
T6664 164-165 , denotes ,
T6665 165-166 CD denotes 4
T6666 166-167 , denotes ,
T6663 167-168 CD denotes 5
T6668 168-169 HYPH denotes -
T6667 169-181 NN denotes triphosphate
T6661 182-190 NN denotes receptor
T6669 191-192 CD denotes 1
T6670 193-194 -LRB- denotes (
T6671 194-199 NN denotes Itpr1
T6672 199-200 -RRB- denotes )
T6673 200-201 . denotes .
R615 T6629 T6630 det The,lesion
R616 T6630 T6633 nsubj lesion,is
R617 T6631 T6630 amod underlying,lesion
R618 T6632 T6630 amod genetic,lesion
R620 T6634 T6630 acl causing,lesion
R622 T6635 T6636 det the,phenotype
R623 T6636 T6634 dobj phenotype,causing
R624 T6637 T6636 compound opt,phenotype
R626 T6638 T6639 det a,deletion
R627 T6639 T6633 attr deletion,is
R628 T6640 T6639 amod homozygous,deletion
R629 T6641 T6642 nmod in,frame
R631 T6642 T6639 compound frame,deletion
R632 T6643 T6642 punct -,frame
R634 T6644 T6639 prep of,deletion
R635 T6645 T6646 nmod exons,43
R636 T6646 T6644 pobj 43,of
R638 T6647 T6646 cc and,43
R639 T6648 T6646 conj 44,43
R640 T6649 T6646 prep of,43
R642 T6650 T6651 det the,Itpr1
R643 T6651 T6649 pobj Itpr1,of
R644 T6652 T6651 compound gene,Itpr1
R646 T6653 T6654 punct (,opt
R647 T6654 T6651 parataxis opt,Itpr1
R648 T6655 T6654 compound Itpr1opt,opt
R650 T6656 T6654 punct /,opt
R651 T6657 T6654 punct ),opt
R652 T6658 T6646 punct ", ",43
R653 T6659 T6646 acl encoding,43
R655 T6660 T6661 nmod inositol,receptor
R656 T6661 T6659 dobj receptor,encoding
R657 T6662 T6663 nummod 1,5
R658 T6663 T6667 nummod 5,triphosphate
R659 T6664 T6663 punct ",",5
R660 T6665 T6663 nummod 4,5
R661 T6666 T6663 punct ",",5
R662 T6667 T6661 compound triphosphate,receptor
R663 T6668 T6667 punct -,triphosphate
R665 T6669 T6661 nummod 1,receptor
R666 T6670 T6671 punct (,Itpr1
R667 T6671 T6661 parataxis Itpr1,receptor
R669 T6672 T6671 punct ),Itpr1
R670 T6673 T6633 punct .,is