PubMed:25157153
Annnotations
PubTator4TogoVar
Id | Subject | Object | Predicate | Lexical cue | proteinmutation |
---|---|---|---|---|---|
25157153_0 | 491-495 | ProteinMutation | denotes | P12A | rs1801282 |
sonoma2
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T0 | 5-13 | VAR | denotes | variants |
T1 | 17-22 | GENE | denotes | PPARG |
T2 | 28-37 | NEGREG | denotes | decreased |
T3 | 38-46 | MPA | denotes | activity |
T4 | 80-90 | REG | denotes | associated |
T5 | 96-105 | POSREG | denotes | increased |
T6 | 121-129 | DISEASE | denotes | diabetes |
T7 | 131-179 | GENE | denotes | Peroxisome proliferator-activated receptor gamma |
T8 | 181-186 | GENE | denotes | PPARG |
T9 | 343-359 | NEGREG | denotes | loss-of-function |
T10 | 361-364 | NEGREG | denotes | LOF |
T11 | 366-375 | VAR | denotes | mutations |
T12 | 379-384 | GENE | denotes | PPARG |
T13 | 398-409 | REG | denotes | cosegregate |
T14 | 415-428 | DISEASE | denotes | lipodystrophy |
T15 | 433-451 | DISEASE | denotes | insulin resistance |
T16 | 433-440 | GENE | denotes | insulin |
T17 | 491-495 | NEGREG | denotes | P12A |
T18 | 496-503 | VAR | denotes | variant |
T19 | 525-534 | NEGREG | denotes | decreased |
T20 | 543-558 | DISEASE | denotes | type 2 diabetes |
T21 | 560-563 | DISEASE | denotes | T2D |
T22 | 587-595 | VAR | denotes | variants |
T23 | 599-604 | GENE | denotes | PPARG |
T24 | 609-616 | NEGREG | denotes | defects |
T25 | 730-735 | GENE | denotes | PPARG |
T26 | 872-877 | GENE | denotes | PPARG |
T27 | 888-891 | GENE | denotes | MAF |
T28 | 1042-1045 | DISEASE | denotes | T2D |
T29 | 1073-1081 | MPA | denotes | function |
T30 | 1092-1100 | VAR | denotes | variants |
T31 | 1221-1228 | NEGREG | denotes | reduced |
T32 | 1229-1237 | MPA | denotes | activity |
T33 | 1279-1282 | NEGREG | denotes | LOF |
T34 | 1283-1291 | VAR | denotes | variants |
T35 | 1296-1306 | REG | denotes | associated |
T36 | 1326-1334 | POSREG | denotes | increase |
T37 | 1346-1349 | DISEASE | denotes | T2D |
T38 | 1521-1528 | VAR | denotes | variant |
T39 | 1532-1537 | GENE | denotes | PPARG |
T40 | 1535-1540 | GENE | denotes | RG th |
T41 | 1543-1550 | NEGREG | denotes | reduces |
T42 | 1551-1559 | MPA | denotes | function |
T43 | 1610-1620 | REG | denotes | associated |
T44 | 1628-1639 | POSREG | denotes | substantial |
T45 | 1648-1651 | DISEASE | denotes | T2D |
R23 | T30 | T31 | CauseOf | variants,reduced |
R24 | T32 | T31 | ThemeOf | activity,reduced |
R25 | T33 | T35 | CauseOf | LOF,associated |
R26 | T33 | T36 | CauseOf | LOF,increase |
R27 | T34 | T33 | CauseOf | variants,LOF |
R28 | T34 | T35 | CauseOf | variants,associated |
R38 | T45 | T44 | ThemeOf | T2D,substantial |
R0 | T0 | T2 | CauseOf | variants,decreased |
R1 | T0 | T5 | CauseOf | variants,increased |
R2 | T1 | T0 | ThemeOf | PPARG,variants |
R3 | T3 | T2 | ThemeOf | activity,decreased |
R4 | T10 | T9 | CauseOf | LOF,loss-of-function |
R5 | T11 | T9 | CauseOf | mutations,loss-of-function |
R6 | T11 | T10 | CauseOf | mutations,LOF |
R7 | T12 | T11 | ThemeOf | PPARG,mutations |
R8 | T14 | T9 | ThemeOf | lipodystrophy,loss-of-function |
R9 | T14 | T10 | ThemeOf | lipodystrophy,LOF |
R10 | T14 | T13 | ThemeOf | lipodystrophy,cosegregate |
R11 | T14 | T19 | ThemeOf | lipodystrophy,decreased |
R12 | T15 | T9 | ThemeOf | insulin resistance,loss-of-function |
R13 | T15 | T10 | ThemeOf | insulin resistance,LOF |
R14 | T15 | T13 | ThemeOf | insulin resistance,cosegregate |
R15 | T15 | T19 | ThemeOf | insulin resistance,decreased |
R16 | T17 | T19 | CauseOf | P12A,decreased |
R17 | T21 | T9 | ThemeOf | T2D,loss-of-function |
R18 | T21 | T10 | ThemeOf | T2D,LOF |
R19 | T21 | T13 | ThemeOf | T2D,cosegregate |
R20 | T21 | T19 | ThemeOf | T2D,decreased |
R21 | T22 | T24 | CauseOf | variants,defects |
R22 | T23 | T22 | ThemeOf | PPARG,variants |
R29 | T34 | T36 | CauseOf | variants,increase |
R30 | T37 | T33 | ThemeOf | T2D,LOF |
R31 | T37 | T35 | ThemeOf | T2D,associated |
R32 | T37 | T36 | ThemeOf | T2D,increase |
R33 | T38 | T41 | CauseOf | variant,reduces |
R34 | T39 | T38 | ThemeOf | PPARG,variant |
R35 | T42 | T41 | ThemeOf | function,reduces |
R36 | T45 | T41 | ThemeOf | T2D,reduces |
R37 | T45 | T43 | ThemeOf | T2D,associated |
PubmedHPO
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 415-428 | HP_0009125 | denotes | lipodystrophy |
T2 | 433-451 | HP_0000855 | denotes | insulin resistance |
DisGeNET5_variant_disease
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
25157153-2#166#170#geners1801282 | 491-495 | geners1801282 | denotes | P12A |
25157153-2#166#170#geners1805192 | 491-495 | geners1805192 | denotes | P12A |
25157153-2#166#170#geners1801282 | 491-495 | geners1801282 | denotes | P12A |
25157153-2#166#170#geners1805192 | 491-495 | geners1805192 | denotes | P12A |
25157153-2#166#170#geners1801282 | 491-495 | geners1801282 | denotes | P12A |
25157153-2#166#170#geners1805192 | 491-495 | geners1805192 | denotes | P12A |
25157153-2#90#103#diseaseC0023787 | 415-428 | diseaseC0023787 | denotes | lipodystrophy |
25157153-2#218#233#diseaseC0011860 | 543-558 | diseaseC0011860 | denotes | type 2 diabetes |
25157153-2#235#238#diseaseC0011860 | 560-563 | diseaseC0011860 | denotes | T2D |
166#170#geners180128290#103#diseaseC0023787 | 25157153-2#166#170#geners1801282 | 25157153-2#90#103#diseaseC0023787 | associated_with | P12A,lipodystrophy |
166#170#geners1801282218#233#diseaseC0011860 | 25157153-2#166#170#geners1801282 | 25157153-2#218#233#diseaseC0011860 | associated_with | P12A,type 2 diabetes |
166#170#geners1801282235#238#diseaseC0011860 | 25157153-2#166#170#geners1801282 | 25157153-2#235#238#diseaseC0011860 | associated_with | P12A,T2D |
166#170#geners180519290#103#diseaseC0023787 | 25157153-2#166#170#geners1805192 | 25157153-2#90#103#diseaseC0023787 | associated_with | P12A,lipodystrophy |
166#170#geners1805192218#233#diseaseC0011860 | 25157153-2#166#170#geners1805192 | 25157153-2#218#233#diseaseC0011860 | associated_with | P12A,type 2 diabetes |
166#170#geners1805192235#238#diseaseC0011860 | 25157153-2#166#170#geners1805192 | 25157153-2#235#238#diseaseC0011860 | associated_with | P12A,T2D |
166#170#geners180128290#103#diseaseC0023787 | 25157153-2#166#170#geners1801282 | 25157153-2#90#103#diseaseC0023787 | associated_with | P12A,lipodystrophy |
166#170#geners1801282218#233#diseaseC0011860 | 25157153-2#166#170#geners1801282 | 25157153-2#218#233#diseaseC0011860 | associated_with | P12A,type 2 diabetes |
166#170#geners1801282235#238#diseaseC0011860 | 25157153-2#166#170#geners1801282 | 25157153-2#235#238#diseaseC0011860 | associated_with | P12A,T2D |
166#170#geners180519290#103#diseaseC0023787 | 25157153-2#166#170#geners1805192 | 25157153-2#90#103#diseaseC0023787 | associated_with | P12A,lipodystrophy |
166#170#geners1805192218#233#diseaseC0011860 | 25157153-2#166#170#geners1805192 | 25157153-2#218#233#diseaseC0011860 | associated_with | P12A,type 2 diabetes |
166#170#geners1805192235#238#diseaseC0011860 | 25157153-2#166#170#geners1805192 | 25157153-2#235#238#diseaseC0011860 | associated_with | P12A,T2D |
166#170#geners180128290#103#diseaseC0023787 | 25157153-2#166#170#geners1801282 | 25157153-2#90#103#diseaseC0023787 | associated_with | P12A,lipodystrophy |
166#170#geners1801282218#233#diseaseC0011860 | 25157153-2#166#170#geners1801282 | 25157153-2#218#233#diseaseC0011860 | associated_with | P12A,type 2 diabetes |
166#170#geners1801282235#238#diseaseC0011860 | 25157153-2#166#170#geners1801282 | 25157153-2#235#238#diseaseC0011860 | associated_with | P12A,T2D |
166#170#geners180519290#103#diseaseC0023787 | 25157153-2#166#170#geners1805192 | 25157153-2#90#103#diseaseC0023787 | associated_with | P12A,lipodystrophy |
166#170#geners1805192218#233#diseaseC0011860 | 25157153-2#166#170#geners1805192 | 25157153-2#218#233#diseaseC0011860 | associated_with | P12A,type 2 diabetes |
166#170#geners1805192235#238#diseaseC0011860 | 25157153-2#166#170#geners1805192 | 25157153-2#235#238#diseaseC0011860 | associated_with | P12A,T2D |
DisGeNET5_gene_disease
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
25157153-0#17#22#gene5468 | 17-22 | gene5468 | denotes | PPARG |
25157153-0#114#129#diseaseC0011860 | 114-129 | diseaseC0011860 | denotes | type 2 diabetes |
25157153-2#54#59#gene5468 | 379-384 | gene5468 | denotes | PPARG |
25157153-2#90#103#diseaseC0023787 | 415-428 | diseaseC0023787 | denotes | lipodystrophy |
17#22#gene5468114#129#diseaseC0011860 | 25157153-0#17#22#gene5468 | 25157153-0#114#129#diseaseC0011860 | associated_with | PPARG,type 2 diabetes |
54#59#gene546890#103#diseaseC0023787 | 25157153-2#54#59#gene5468 | 25157153-2#90#103#diseaseC0023787 | associated_with | PPARG,lipodystrophy |
kaiyin_test
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T8 | 343-359 | NegReg | denotes | loss-of-function |
T4 | 366-375 | Var | denotes | mutations |
T5 | 379-384 | Gene | denotes | PPARG |
T6 | 415-428 | Disease | denotes | lipodystrophy |
T7 | 433-451 | Disease | denotes | insulin resistance |
T1 | 491-503 | Var | denotes | P12A variant |
T2 | 525-534 | NegReg | denotes | decreased |
T12 | 543-558 | Disease | denotes | type 2 diabetes |
T10 | 1521-1528 | Var | denotes | variant |
T9 | 1532-1537 | Gene | denotes | PPARG |
T11 | 1543-1550 | NegReg | denotes | reduces |
T15 | 1551-1602 | CPA | denotes | function in a human adipocyte differentiation assay |
T13 | 1610-1620 | Reg | denotes | associated |
T14 | 1648-1651 | Disease | denotes | T2D |
R1 | T5 | T4 | ThemeOf | PPARG,mutations |
R10 | T10 | T13 | CauseOf | variant,associated |
R11 | T14 | T13 | ThemeOf | T2D,associated |
R12 | T5 | T1 | ThemeOf | PPARG,P12A variant |
R2 | T4 | T8 | CauseOf | mutations,loss-of-function |
R3 | T6 | T8 | ThemeOf | lipodystrophy,loss-of-function |
R4 | T7 | T8 | ThemeOf | insulin resistance,loss-of-function |
R5 | T1 | T2 | CauseOf | P12A variant,decreased |
R6 | T12 | T2 | ThemeOf | type 2 diabetes,decreased |
R7 | T9 | T10 | ThemeOf | PPARG,variant |
R8 | T10 | T11 | CauseOf | variant,reduces |
R9 | T15 | T11 | ThemeOf | function in a human adipocyte differentiation assay,reduces |
name_no
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T8 | 343-359 | NegReg | denotes | loss-of-function |
T4 | 366-375 | Var | denotes | mutations |
T5 | 379-384 | Gene | denotes | PPARG |
T6 | 415-428 | Disease | denotes | lipodystrophy |
T7 | 433-451 | Disease | denotes | insulin resistance |
T1 | 491-503 | Var | denotes | P12A variant |
T2 | 525-534 | NegReg | denotes | decreased |
T12 | 543-558 | Disease | denotes | type 2 diabetes |
T10 | 1521-1528 | Var | denotes | variant |
T9 | 1532-1537 | Gene | denotes | PPARG |
T11 | 1543-1550 | NegReg | denotes | reduces |
T15 | 1551-1602 | CPA | denotes | function in a human adipocyte differentiation assay |
T13 | 1610-1620 | Reg | denotes | associated |
T14 | 1648-1651 | Disease | denotes | T2D |
R1 | T5 | T4 | ThemeOf | PPARG,mutations |
R10 | T10 | T13 | CauseOf | variant,associated |
R11 | T14 | T13 | ThemeOf | T2D,associated |
R12 | T5 | T1 | ThemeOf | PPARG,P12A variant |
R2 | T4 | T8 | CauseOf | mutations,loss-of-function |
R3 | T6 | T8 | ThemeOf | lipodystrophy,loss-of-function |
R4 | T7 | T8 | ThemeOf | insulin resistance,loss-of-function |
R5 | T1 | T2 | CauseOf | P12A variant,decreased |
R6 | T12 | T2 | ThemeOf | type 2 diabetes,decreased |
R7 | T9 | T10 | ThemeOf | PPARG,variant |
R8 | T10 | T11 | CauseOf | variant,reduces |
R9 | T15 | T11 | ThemeOf | function in a human adipocyte differentiation assay,reduces |