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sonoma2

Id Subject Object Predicate Lexical cue
T0 4-22 VAR denotes mutation m.13513G>
T1 13-23 VAR denotes m.13513G>A
T2 24-31 NEGREG denotes impairs
T3 32-48 CPA denotes cardiac function
T4 50-58 POSREG denotes favoring
T5 61-74 CPA denotes neuroectoderm
T6 75-85 CPA denotes commitment
T7 119-142 DISEASE denotes Mitochondrial disorders
T8 122-145 DISEASE denotes ochondrial disorders (M
T9 144-147 DISEASE denotes MDs
T10 147-150 DISEASE denotes ) a
T11 149-154 REG denotes arise
T12 175-204 DISEASE denotes piratory chain dysfunction. W
T13 190-201 VAR denotes dysfunction
T14 214-217 DISEASE denotes MDs
T15 217-220 DISEASE denotes ca
T16 222-228 REG denotes affect
T17 250-257 REG denotes involve
T18 299-307 REG denotes affected
T19 321-326 CPA denotes heart
T20 334-340 CPA denotes muscle
T21 369-379 REG denotes associated
T22 388-401 DISEASE denotes eroplasmic mu
T23 399-408 VAR denotes mutations
T24 461-468 VAR denotes mutated
T25 511-518 REG denotes produce
T26 519-526 DISEASE denotes disease
T27 779-788 REG denotes influence
T28 792-810 CPA denotes cardiac commitment
T29 841-851 VAR denotes m.13513G>A
T30 849-860 VAR denotes >A mutation
T31 885-893 VAR denotes mutation
T32 926-931 REG denotes cause
T33 935-949 DISEASE denotes Leigh syndrome
T34 941-955 DISEASE denotes syndrome (LS)
T35 951-953 DISEASE denotes LS
T36 971-981 REG denotes associated
T37 987-1003 DISEASE denotes cardiac problems
T38 1133-1148 DISEASE denotes cardiac disease
T39 1139-1154 DISEASE denotes c disease in LS
T40 1152-1154 DISEASE denotes LS
T41 1161-1179 VAR denotes mutation m.13513G>
T42 1170-1180 VAR denotes m.13513G>A
T43 1184-1189 POSREG denotes above
T44 1274-1285 NEGREG denotes inefficient
T45 1286-1319 CPA denotes epithelial-mesenchymal transition
T46 1369-1393 CPA denotes neuroectodermal lineages
T47 1410-1414 REG denotes rise
T48 1422-1427 CPA denotes brain
T49 1443-1451 VAR denotes mutation
T50 1455-1460 NEGREG denotes below
T51 1486-1502 DISEASE denotes onal CM are gene
T52 1491-1493 CPA denotes CM
T53 1576-1586 VAR denotes m.13513G>A
T54 1584-1595 VAR denotes >A mutation
T55 1603-1626 CPA denotes cardiac differentiation
T56 1686-1700 CPA denotes neuropathology
T57 1726-1728 DISEASE denotes MD
T58 1768-1775 REG denotes present
R35 T41 T44 CauseOf mutation m.13513G>,inefficient
R36 T42 T43 CauseOf m.13513G>A,above
R37 T42 T44 CauseOf m.13513G>A,inefficient
R0 T0 T2 CauseOf mutation m.13513G>,impairs
R1 T0 T4 CauseOf mutation m.13513G>,favoring
R2 T1 T2 CauseOf m.13513G>A,impairs
R3 T1 T4 CauseOf m.13513G>A,favoring
R4 T3 T2 ThemeOf cardiac function,impairs
R5 T5 T4 ThemeOf neuroectoderm,favoring
R6 T5 T6 ThemeOf neuroectoderm,commitment
R7 T6 T4 ThemeOf commitment,favoring
R8 T7 T9 ThemeOf Mitochondrial disorders,MDs
R9 T7 T11 ThemeOf Mitochondrial disorders,arise
R10 T9 T11 ThemeOf MDs,arise
R11 T13 T9 CauseOf dysfunction,MDs
R12 T13 T11 CauseOf dysfunction,arise
R13 T13 T18 CauseOf dysfunction,affected
R14 T14 T16 ThemeOf MDs,affect
R15 T14 T17 ThemeOf MDs,involve
R16 T14 T18 ThemeOf MDs,affected
R17 T19 T18 ThemeOf heart,affected
R18 T20 T17 ThemeOf muscle,involve
R19 T20 T18 ThemeOf muscle,affected
R20 T23 T21 CauseOf mutations,associated
R21 T24 T25 CauseOf mutated,produce
R22 T26 T25 ThemeOf disease,produce
R23 T28 T27 ThemeOf cardiac commitment,influence
R24 T29 T27 CauseOf m.13513G>A,influence
R25 T30 T27 CauseOf >A mutation,influence
R26 T31 T32 CauseOf mutation,cause
R27 T31 T36 CauseOf mutation,associated
R28 T33 T32 ThemeOf Leigh syndrome,cause
R29 T33 T36 ThemeOf Leigh syndrome,associated
R30 T35 T32 ThemeOf LS,cause
R31 T37 T32 ThemeOf cardiac problems,cause
R32 T37 T36 ThemeOf cardiac problems,associated
R33 T40 T38 ThemeOf LS,cardiac disease
R34 T41 T43 CauseOf mutation m.13513G>,above
R38 T43 T44 CauseOf above,inefficient
R39 T45 T44 ThemeOf epithelial-mesenchymal transition,inefficient
R40 T48 T47 ThemeOf brain,rise
R41 T49 T50 CauseOf mutation,below
R42 T56 T58 ThemeOf neuropathology,present
R43 T57 T58 ThemeOf MD,present