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PubMed:29880043 JSONTXT

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue
T0 25-38 DISEASE denotes ganglioglioma
T1 40-53 DISEASE denotes Ganglioglioma
T2 66-72 REG denotes common
T4 73-92 DISEASE denotes epilepsy-associated
T3 73-101 DISEASE denotes epilepsy-associated neoplasm
T5 93-101 DISEASE denotes neoplasm
T6 152-164 DISEASE denotes brain tumors
T7 184-198 DISEASE denotes gangliogliomas
T8 212-218 REG denotes harbor
T9 223-233 POSREG denotes activating
T10 236-241 VAR denotes V600E
T11 242-250 VAR denotes mutation
T12 258-262 GENE denotes BRAF
T13 602-616 DISEASE denotes gangliogliomas
T14 629-637 REG denotes harbored
T15 638-647 VAR denotes mutations
T16 661-669 POSREG denotes activate
T17 678-702 PATHWAY denotes kinase signaling pathway
T18 722-726 GENE denotes BRAF
T19 735-743 VAR denotes mutation
T20 752-759 VAR denotes variant
T21 760-764 GENE denotes BRAF
T22 765-773 VAR denotes mutation
T23 813-823 VAR denotes insertions
T24 829-833 VAR denotes R506
T25 882-886 GENE denotes BRAF
T26 887-893 VAR denotes fusion
T27 889-893 GENE denotes sion
T28 907-915 VAR denotes mutation
T29 909-913 GENE denotes tati
T30 924-928 GENE denotes RAF1
T31 929-935 VAR denotes fusion
T32 931-935 GENE denotes sion
T33 944-953 VAR denotes biallelic
T34 954-957 GENE denotes NF1
T35 958-966 VAR denotes mutation
T36 961-964 GENE denotes ati
T37 979-986 GENE denotes FGFR1/2
T38 986-993 GENE denotes altera
T39 987-998 VAR denotes alterations
T40 1006-1020 DISEASE denotes gangliogliomas
T41 1026-1030 GENE denotes BRAF
T42 1033-1037 GENE denotes V600
T43 1039-1047 VAR denotes mutation
T44 1063-1069 GENE denotes CDKN2A
T45 1070-1076 GENE denotes homozy
T46 1081-1089 VAR denotes deletion
T47 1111-1119 REG denotes harbored
T48 1132-1140 VAR denotes mutation
T49 1144-1148 GENE denotes PTEN
T50 1151-1155 GENE denotes ther
T51 1186-1195 VAR denotes mutations
T52 1197-1204 VAR denotes fusions
T53 1206-1220 VAR denotes amplifications
T54 1225-1234 VAR denotes deletions
T55 1240-1250 REG denotes identified
T56 1271-1277 DISEASE denotes tumors
T57 1278-1284 DISEASE denotes Among
T58 1293-1307 DISEASE denotes gangliogliomas
T59 1326-1344 PATHWAY denotes MAP kinase pathway
T60 1345-1356 VAR denotes alterations
T61 1373-1398 DISEASE denotes epilepsy-associated tumor
T62 1380-1399 DISEASE denotes y-associated tumor
T63 1400-1405 DISEASE denotes n the
T64 1450-1456 REG denotes harbor
T65 1465-1474 GENE denotes ABL2-GAB2
T66 1472-1481 GENE denotes B2 gene f
T67 1480-1486 VAR denotes fusion
T68 1511-1522 VAR denotes alterations
T69 1548-1559 REG denotes association
T70 1664-1677 DISEASE denotes ganglioglioma
T71 1681-1694 REG denotes characterized
T72 1706-1717 VAR denotes alterations
T73 1723-1731 POSREG denotes activate
T74 1740-1754 PATHWAY denotes kinase pathway
T75 1795-1801 REG denotes harbor
T76 1824-1835 VAR denotes alterations
T77 1844-1850 GENE denotes CDKN2A
T79 1851-1857 GENE denotes deleti
T78 1851-1859 VAR denotes deletion
R0 T0 T2 ThemeOf ganglioglioma,common
R1 T1 T2 ThemeOf Ganglioglioma,common
R10 T13 T14 ThemeOf gangliogliomas,harbored
R100 T67 T64 ThemeOf fusion,harbor
R101 T68 T69 CauseOf alterations,association
R102 T70 T71 ThemeOf ganglioglioma,characterized
R103 T70 T73 ThemeOf ganglioglioma,activate
R104 T70 T75 ThemeOf ganglioglioma,harbor
R105 T72 T71 CauseOf alterations,characterized
R106 T72 T73 CauseOf alterations,activate
R107 T74 T73 ThemeOf kinase pathway,activate
R108 T74 T75 ThemeOf kinase pathway,harbor
R109 T76 T75 ThemeOf alterations,harbor
R11 T14 T16 CauseOf harbored,activate
R110 T76 T73 CauseOf alterations,activate
R111 T77 T75 ThemeOf CDKN2A,harbor
R112 T77 T76 ThemeOf CDKN2A,alterations
R113 T77 T78 ThemeOf CDKN2A,deletion
R114 T78 T73 CauseOf deletion,activate
R115 T78 T75 ThemeOf deletion,harbor
R116 T78 T76 ThemeOf deletion,alterations
R12 T15 T14 ThemeOf mutations,harbored
R13 T15 T16 CauseOf mutations,activate
R14 T17 T14 ThemeOf kinase signaling pathway,harbored
R15 T17 T16 ThemeOf kinase signaling pathway,activate
R16 T18 T19 ThemeOf BRAF,mutation
R17 T18 T22 ThemeOf BRAF,mutation
R18 T18 T23 ThemeOf BRAF,insertions
R19 T18 T26 ThemeOf BRAF,fusion
R2 T1 T3 ThemeOf Ganglioglioma,epilepsy-associated neoplasm
R20 T19 T16 CauseOf mutation,activate
R21 T20 T16 CauseOf variant,activate
R22 T20 T22 ThemeOf variant,mutation
R23 T21 T19 ThemeOf BRAF,mutation
R24 T21 T20 ThemeOf BRAF,variant
R25 T21 T22 ThemeOf BRAF,mutation
R26 T21 T23 ThemeOf BRAF,insertions
R27 T21 T24 ThemeOf BRAF,R506
R28 T21 T26 ThemeOf BRAF,fusion
R29 T21 T28 ThemeOf BRAF,mutation
R3 T3 T2 ThemeOf epilepsy-associated neoplasm,common
R30 T21 T31 ThemeOf BRAF,fusion
R31 T21 T35 ThemeOf BRAF,mutation
R32 T21 T39 ThemeOf BRAF,alterations
R33 T22 T16 CauseOf mutation,activate
R34 T23 T16 CauseOf insertions,activate
R35 T24 T16 CauseOf R506,activate
R36 T25 T19 ThemeOf BRAF,mutation
R37 T25 T22 ThemeOf BRAF,mutation
R38 T25 T23 ThemeOf BRAF,insertions
R39 T25 T24 ThemeOf BRAF,R506
R4 T7 T8 ThemeOf gangliogliomas,harbor
R40 T25 T26 ThemeOf BRAF,fusion
R41 T25 T28 ThemeOf BRAF,mutation
R42 T25 T31 ThemeOf BRAF,fusion
R43 T25 T33 ThemeOf BRAF,biallelic
R44 T25 T35 ThemeOf BRAF,mutation
R45 T25 T39 ThemeOf BRAF,alterations
R46 T26 T16 CauseOf fusion,activate
R47 T28 T16 CauseOf mutation,activate
R48 T30 T19 ThemeOf RAF1,mutation
R49 T30 T22 ThemeOf RAF1,mutation
R5 T7 T9 ThemeOf gangliogliomas,activating
R50 T30 T23 ThemeOf RAF1,insertions
R51 T30 T26 ThemeOf RAF1,fusion
R52 T30 T28 ThemeOf RAF1,mutation
R53 T30 T31 ThemeOf RAF1,fusion
R54 T30 T33 ThemeOf RAF1,biallelic
R55 T30 T35 ThemeOf RAF1,mutation
R56 T30 T39 ThemeOf RAF1,alterations
R57 T31 T16 CauseOf fusion,activate
R58 T33 T14 CauseOf biallelic,harbored
R59 T33 T16 CauseOf biallelic,activate
R6 T10 T9 CauseOf V600E,activating
R60 T34 T19 ThemeOf NF1,mutation
R61 T34 T22 ThemeOf NF1,mutation
R62 T34 T23 ThemeOf NF1,insertions
R63 T34 T26 ThemeOf NF1,fusion
R64 T34 T28 ThemeOf NF1,mutation
R65 T34 T31 ThemeOf NF1,fusion
R66 T34 T33 ThemeOf NF1,biallelic
R67 T34 T35 ThemeOf NF1,mutation
R68 T34 T39 ThemeOf NF1,alterations
R69 T35 T16 CauseOf mutation,activate
R7 T11 T9 CauseOf mutation,activating
R70 T37 T19 ThemeOf FGFR1/2,mutation
R71 T37 T22 ThemeOf FGFR1/2,mutation
R72 T37 T23 ThemeOf FGFR1/2,insertions
R73 T37 T26 ThemeOf FGFR1/2,fusion
R74 T37 T28 ThemeOf FGFR1/2,mutation
R75 T37 T31 ThemeOf FGFR1/2,fusion
R76 T37 T33 ThemeOf FGFR1/2,biallelic
R77 T37 T35 ThemeOf FGFR1/2,mutation
R78 T37 T39 ThemeOf FGFR1/2,alterations
R79 T39 T16 CauseOf alterations,activate
R8 T12 T10 ThemeOf BRAF,V600E
R80 T40 T43 ThemeOf gangliogliomas,mutation
R81 T40 T47 ThemeOf gangliogliomas,harbored
R82 T41 T43 ThemeOf BRAF,mutation
R83 T41 T46 ThemeOf BRAF,deletion
R84 T44 T43 ThemeOf CDKN2A,mutation
R85 T44 T46 ThemeOf CDKN2A,deletion
R86 T48 T47 ThemeOf mutation,harbored
R87 T49 T48 ThemeOf PTEN,mutation
R88 T51 T55 CauseOf mutations,identified
R89 T54 T55 ThemeOf deletions,identified
R9 T12 T11 ThemeOf BRAF,mutation
R90 T56 T55 ThemeOf tumors,identified
R91 T58 T60 ThemeOf gangliogliomas,alterations
R92 T58 T64 ThemeOf gangliogliomas,harbor
R93 T59 T60 ThemeOf MAP kinase pathway,alterations
R94 T59 T64 ThemeOf MAP kinase pathway,harbor
R95 T60 T64 ThemeOf alterations,harbor
R96 T61 T60 ThemeOf epilepsy-associated tumor,alterations
R97 T61 T64 ThemeOf epilepsy-associated tumor,harbor
R98 T65 T64 ThemeOf ABL2-GAB2,harbor
R99 T65 T67 ThemeOf ABL2-GAB2,fusion