> top > docs > PMC:1189073 > spans > 14484-15138 > annotations

PMC:1189073 / 14484-15138 JSONTXT

Annnotations TAB JSON ListView MergeView

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
T8613 505-511 NCBITaxon:9606 denotes humans
T8614 523-530 SO_EXT:0001023 denotes alleles
T8615 534-538 PR_EXT:000004182 denotes Aqp2
T8616 596-607 GO_EXT:biological_movement_or_translocation_process denotes translocate
T8617 615-621 GO:0045177 denotes apical
T8618 622-626 CL_GO_EXT:cell denotes cell
T8619 622-634 GO:0009986 denotes cell surface
T8620 638-646 GO_EXT:reaction_or_response denotes response
T8621 650-653 CHEBI_PR_EXT:arginine_vasopressin denotes AVP

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
T8225 505-511 NCBITaxon:9606 denotes humans
T8226 523-530 SO:0001023 denotes alleles
T8227 534-538 PR:000004182 denotes Aqp2
T8228 615-621 GO:0045177 denotes apical
T8229 622-634 GO:0009986 denotes cell surface

craft-sa-dev

Id Subject Object Predicate Lexical cue
T10090 0-654 sentence denotes Figure 3 Immunoblot Analyses of AQP2 from Mouse Kidneys (A) Western blot analyses of total kidney membranes from littermate mice. An intermediate form of AQP2 at 31 kDa was identified in kidney membranes from a mutant mouse (Mut) and partially in a heterozygous mouse (Het). (B) Total kidney membranes were subjected to endoglycosidase H treatment (Endo H) prior to Western blotting. High-mannose (h.m.) glycosylated proteins that have not exited the ER are sensitive to endoglycosidase H digestion. In humans, recessive alleles of Aqp2 are postulated to cause NDI because they do not properly translocate to the apical cell surface in response to AVP.
T10091 502-504 IN denotes In
T10092 543-553 VBN denotes postulated
T10093 505-511 NNS denotes humans
T10094 511-513 , denotes ,
T10095 513-522 JJ denotes recessive
T10096 523-530 NNS denotes alleles
T10097 531-533 IN denotes of
T10098 534-538 NN denotes Aqp2
T10099 539-542 VBP denotes are
T10100 554-556 TO denotes to
T10101 557-562 VB denotes cause
T10102 563-566 NN denotes NDI
T10103 567-574 IN denotes because
T10104 596-607 VB denotes translocate
T10105 575-579 PRP denotes they
T10106 580-582 VBP denotes do
T10107 583-586 RB denotes not
T10108 587-595 RB denotes properly
T10109 608-610 IN denotes to
T10110 611-614 DT denotes the
T10111 627-634 NN denotes surface
T10112 615-621 JJ denotes apical
T10113 622-626 NN denotes cell
T10114 635-637 IN denotes in
T10115 638-646 NN denotes response
T10116 647-649 IN denotes to
T10117 650-653 NN denotes AVP
T10118 653-654 . denotes .
R1975 T10091 T10092 prep In,postulated
R1976 T10093 T10091 pobj humans,In
R1978 T10094 T10092 punct ", ",postulated
R1979 T10095 T10096 amod recessive,alleles
R1980 T10096 T10092 nsubjpass alleles,postulated
R1981 T10097 T10096 prep of,alleles
R1983 T10098 T10097 pobj Aqp2,of
R1984 T10099 T10092 auxpass are,postulated
R1985 T10100 T10101 aux to,cause
R1987 T10101 T10092 xcomp cause,postulated
R1988 T10102 T10101 dobj NDI,cause
R1989 T10103 T10104 mark because,translocate
R1992 T10104 T10101 advcl translocate,cause
R1993 T10105 T10104 nsubj they,translocate
R1995 T10106 T10104 aux do,translocate
R1996 T10107 T10104 neg not,translocate
R1997 T10108 T10104 advmod properly,translocate
R1998 T10109 T10104 prep to,translocate
R1999 T10110 T10111 det the,surface
R2001 T10111 T10109 pobj surface,to
R2002 T10112 T10111 amod apical,surface
R2003 T10113 T10111 compound cell,surface
R2004 T10114 T10104 prep in,translocate
R2006 T10115 T10114 pobj response,in
R2007 T10116 T10115 prep to,response
R2009 T10117 T10116 pobj AVP,to
R2010 T10118 T10092 punct .,postulated