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PMC:2806624 / 4484-4687 JSONTXT

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pmc-enju-pas

Id Subject Object Predicate Lexical cue
T1816 9-10 DT denotes a
T1817 11-19 JJ denotes frequent
T1818 20-26 NN denotes target
T1819 27-30 IN denotes for
T1820 31-42 JJ denotes chromosomal
T1821 43-57 NN denotes translocations
T1822 58-68 VB denotes associated
T1823 69-73 IN denotes with
T1824 74-83 NN denotes leukemias
T1825 84-85 -LRB- denotes (
T1826 85-89 NNP denotes Look
T1827 89-90 -COMMA- denotes ,
T1828 91-95 CD denotes 1997
T1829 95-96 -RRB- denotes )
T1830 96-97 -COMMA- denotes ,
T1831 98-119 NN denotes and RUNX3 methylation
T1832 120-123 CC denotes and
T1833 124-133 NN denotes silencing
T1834 134-136 VB denotes is
T1835 137-145 VB denotes observed
T1836 146-148 IN denotes in
T1837 149-156 JJ denotes various
T1838 157-162 JJ denotes human
T1839 163-173 JJ denotes epithelial
T1840 174-181 NN denotes cancers
T1841 182-183 -LRB- denotes (
T1842 183-188 NNP denotes Blyth
T1843 189-191 FW denotes et
T1844 192-195 FW denotes al.
T1845 195-196 -COMMA- denotes ,
T1846 197-201 CD denotes 2005
T1847 201-202 -RRB- denotes )
R1397 T1818 T1817 arg1Of target,frequent
R1398 T1818 T1819 arg1Of target,for
R1399 T1818 T1830 arg1Of target,","
R1400 T1821 T1819 arg2Of translocations,for
R1401 T1821 T1820 arg1Of translocations,chromosomal
R1402 T1821 T1822 arg2Of translocations,associated
R1403 T1822 T1823 arg1Of associated,with
R1404 T1822 T1825 arg1Of associated,(
R1405 T1824 T1823 arg2Of leukemias,with
R1406 T1826 T1825 arg2Of Look,(
R1407 T1826 T1827 arg1Of Look,","
R1408 T1826 T1828 arg1Of Look,1997
R1409 T1829 T1825 arg3Of ),(
R1411 T1830 T1816 arg1Of ",",a
R1412 T1831 T1830 arg2Of and RUNX3 methylation,","
R1413 T1833 T1834 arg1Of silencing,is
R1414 T1833 T1835 arg2Of silencing,observed
R1415 T1835 T1834 arg2Of observed,is
R1416 T1835 T1836 arg1Of observed,in
R1417 T1835 T1841 arg1Of observed,(
R1418 T1840 T1836 arg2Of cancers,in
R1419 T1840 T1837 arg1Of cancers,various
R1420 T1840 T1838 arg1Of cancers,human
R1421 T1840 T1839 arg1Of cancers,epithelial
R1422 T1842 T1841 arg2Of Blyth,(
R1423 T1842 T1843 arg1Of Blyth,et
R1424 T1842 T1844 arg1Of Blyth,al.
R1425 T1842 T1845 arg1Of Blyth,","
R1426 T1846 T1845 arg2Of 2005,","
R1427 T1847 T1841 arg3Of ),(

bionlp-st-ge-2016-spacy-parsed

Id Subject Object Predicate Lexical cue
T2657 0-8 NNS denotes RUNX1 is
T2658 9-10 DT denotes a
T2659 11-19 JJ denotes frequent
T2660 20-26 NN denotes target
T2661 27-30 IN denotes for
T2662 31-42 JJ denotes chromosomal
T2663 43-57 NNS denotes translocations
T2664 58-68 VBN denotes associated
T2665 69-73 IN denotes with
T2666 74-83 NNS denotes leukemias
T2667 84-85 -LRB- denotes (
T2668 85-89 VB denotes Look
T2669 89-90 , denotes ,
T2670 91-95 CD denotes 1997
T2671 95-96 -RRB- denotes )
T2672 96-97 , denotes ,
T2673 98-119 NN denotes and RUNX3 methylation
T2674 120-123 CC denotes and
T2675 124-133 NN denotes silencing
T2676 134-136 VBZ denotes is
T2677 137-145 VBN denotes observed
T2678 146-148 IN denotes in
T2679 149-156 JJ denotes various
T2680 157-162 JJ denotes human
T2681 163-173 JJ denotes epithelial
T2682 174-181 NNS denotes cancers
T2683 182-183 -LRB- denotes (
T2684 183-188 NNP denotes Blyth
T2685 189-191 FW denotes et
T2686 192-195 FW denotes al.
T2687 195-196 , denotes ,
T2688 197-201 CD denotes 2005
T2689 201-202 -RRB- denotes )
T2690 202-203 . denotes .
R2072 T2657 T2677 nsubjpass RUNX1 is,observed
R2073 T2658 T2660 det a,target
R2074 T2659 T2660 amod frequent,target
R2076 T2660 T2657 appos target,RUNX1 is
R2077 T2661 T2660 prep for,target
R2078 T2662 T2663 amod chromosomal,translocations
R2080 T2663 T2661 pobj translocations,for
R2081 T2664 T2663 acl associated,translocations
R2083 T2665 T2664 prep with,associated
R2084 T2666 T2665 pobj leukemias,with
R2085 T2667 T2666 punct (,leukemias
R2087 T2668 T2668 ROOT Look,Look
R2088 T2669 T2668 punct ",",Look
R2089 T2670 T2668 npadvmod 1997,Look
R2091 T2671 T2668 punct ),Look
R2092 T2672 T2668 punct ",",Look
R2094 T2673 T2677 nsubjpass and RUNX3 methylation,observed
R2095 T2674 T2673 cc and,and RUNX3 methylation
R2097 T2675 T2673 conj silencing,and RUNX3 methylation
R2098 T2676 T2677 auxpass is,observed
R2099 T2677 T2677 ROOT observed,observed
R2101 T2678 T2677 prep in,observed
R2102 T2679 T2682 amod various,cancers
R2103 T2680 T2682 amod human,cancers
R2105 T2681 T2682 amod epithelial,cancers
R2106 T2682 T2678 pobj cancers,in
R2107 T2683 T2686 punct (,al.
R2108 T2684 T2686 compound Blyth,al.
R2109 T2685 T2686 nmod et,al.
R2110 T2686 T2677 dep al.,observed
R2112 T2687 T2686 punct ",",al.
R2113 T2688 T2686 npadvmod 2005,al.
R2114 T2689 T2686 punct ),al.
R2116 T2690 T2677 punct .,observed

GO-CC

Id Subject Object Predicate Lexical cue
T3018 31-42 http://purl.obolibrary.org/obo/GO_0005694 denotes chromosomal

sentences

Id Subject Object Predicate Lexical cue
T27 0-203 Sentence denotes RUNX1 is a frequent target for chromosomal translocations associated with leukemias (Look, 1997), and RUNX3 methylation and silencing is observed in various human epithelial cancers (Blyth et al., 2005).

events-check-again

Id Subject Object Predicate Lexical cue
T3261 0-5 Protein denotes RUNX1
T3262 102-107 Protein denotes RUNX3

bionlp-st-ge-2016-reference

Id Subject Object Predicate Lexical cue
T1251 0-5 Protein denotes RUNX1
T1252 102-107 Protein denotes RUNX3

test2

Id Subject Object Predicate Lexical cue
T1160 0-8 Protein denotes RUNX1 is
T1161 98-119 Protein denotes and RUNX3 methylation
T1162 124-133 Negative_regulation denotes silencing
R811 T1161 T1162 themeOf and RUNX3 methylation,silencing