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AGAC_v3

Id Subject Object Predicate Lexical cue
T2 139-158 Var denotes Biallelic mutations
T1 212-216 Gene denotes ALS2
T3 223-228 Reg denotes cause
T4 310-364 Disease denotes infantile-onset ascending hereditary spastic paralysis
T5 374-408 Disease denotes juvenile primary lateral sclerosis
T6 421-459 Disease denotes juvenile amyotrophic lateral sclerosis
T7 473-482 Reg denotes caused by
T8 483-557 CPA denotes retrograde degeneration of the upper motor neurons of the pyramidal tracts
T9 626-631 Disease denotes IAHSP
T10 685-693 Reg denotes carrying
T11 709-720 Var denotes c.1640+1G>A
T12 741-745 Gene denotes ALS2
R9 T11 T10 CauseOf c.1640+1G>A,carrying
R8 T12 T11 ThemeOf ALS2,c.1640+1G>A
R7 T5 T3 ThemeOf juvenile primary lateral sclerosis,cause
R6 T6 T3 ThemeOf juvenile amyotrophic lateral sclerosis,cause
R5 T4 T3 ThemeOf infantile-onset ascending hereditary spastic paralysis,cause
R4 T7 T3 CauseOf caused by,cause
R3 T8 T7 ThemeOf retrograde degeneration of the upper motor neurons of the pyramidal tracts,caused by
R2 T2 T7 CauseOf Biallelic mutations,caused by
R10 T9 T10 ThemeOf IAHSP,carrying
R1 T1 T2 ThemeOf ALS2,Biallelic mutations

AGAC-FULL-201905

Id Subject Object Predicate Lexical cue
T2 139-158 Var denotes Biallelic mutations
T1 212-216 Gene denotes ALS2
T3 223-228 Reg denotes cause
T4 310-364 Disease denotes infantile-onset ascending hereditary spastic paralysis
T5 374-408 Disease denotes juvenile primary lateral sclerosis
T6 421-459 Disease denotes juvenile amyotrophic lateral sclerosis
T7 473-482 Reg denotes caused by
T8 483-557 CPA denotes retrograde degeneration of the upper motor neurons of the pyramidal tracts
T9 626-631 Disease denotes IAHSP
T10 685-693 Reg denotes carrying
T11 709-720 Var denotes c.1640+1G>A
T12 741-745 Gene denotes ALS2
R1 T1 T2 ThemeOf ALS2,Biallelic mutations
R10 T9 T10 ThemeOf IAHSP,carrying
R2 T2 T7 CauseOf Biallelic mutations,caused by
R3 T8 T7 ThemeOf retrograde degeneration of the upper motor neurons of the pyramidal tracts,caused by
R4 T7 T3 CauseOf caused by,cause
R5 T4 T3 ThemeOf infantile-onset ascending hereditary spastic paralysis,cause
R6 T6 T3 ThemeOf juvenile amyotrophic lateral sclerosis,cause
R7 T5 T3 ThemeOf juvenile primary lateral sclerosis,cause
R8 T12 T11 ThemeOf ALS2,c.1640+1G>A
R9 T11 T10 CauseOf c.1640+1G>A,carrying

AGAC2_PubMed7000

Id Subject Object Predicate Lexical cue
T1 212-216 Gene denotes ALS2
T2 139-158 Var denotes Biallelic mutations
T3 223-228 Reg denotes cause
T4 310-364 Disease denotes infantile-onset ascending hereditary spastic paralysis
T5 374-408 Disease denotes juvenile primary lateral sclerosis
T6 421-459 Disease denotes juvenile amyotrophic lateral sclerosis
T7 473-482 Reg denotes caused by
T8 483-557 CPA denotes retrograde degeneration of the upper motor neurons of the pyramidal tracts
T9 626-631 Disease denotes IAHSP
T10 685-693 Reg denotes carrying
T11 709-720 Var denotes c.1640+1G>A
T12 741-745 Gene denotes ALS2
R1 T1 T2 ThemeOf ALS2,Biallelic mutations
R2 T2 T7 CauseOf Biallelic mutations,caused by
R3 T8 T7 ThemeOf retrograde degeneration of the upper motor neurons of the pyramidal tracts,caused by
R4 T7 T3 CauseOf caused by,cause
R5 T4 T3 ThemeOf infantile-onset ascending hereditary spastic paralysis,cause
R6 T6 T3 ThemeOf juvenile amyotrophic lateral sclerosis,cause
R7 T5 T3 ThemeOf juvenile primary lateral sclerosis,cause
R8 T12 T11 ThemeOf ALS2,c.1640+1G>A
R9 T11 T10 CauseOf c.1640+1G>A,carrying
R10 T9 T10 ThemeOf IAHSP,carrying

AGAC_answer

Id Subject Object Predicate Lexical cue
T2 139-158 Var denotes Biallelic mutations
T1 212-216 Gene denotes ALS2
T3 223-228 Reg denotes cause
T4 310-364 Disease denotes infantile-onset ascending hereditary spastic paralysis
T5 374-408 Disease denotes juvenile primary lateral sclerosis
T6 421-459 Disease denotes juvenile amyotrophic lateral sclerosis
T7 473-482 Reg denotes caused by
T8 483-557 CPA denotes retrograde degeneration of the upper motor neurons of the pyramidal tracts
T9 626-631 Disease denotes IAHSP
T10 685-693 Reg denotes carrying
T11 709-720 Var denotes c.1640+1G>A
T12 741-745 Gene denotes ALS2
R1 T1 T2 ThemeOf ALS2,Biallelic mutations
R10 T9 T10 ThemeOf IAHSP,carrying
R2 T2 T7 CauseOf Biallelic mutations,caused by
R3 T8 T7 ThemeOf retrograde degeneration of the upper motor neurons of the pyramidal tracts,caused by
R4 T7 T3 CauseOf caused by,cause
R5 T4 T3 ThemeOf infantile-onset ascending hereditary spastic paralysis,cause
R6 T6 T3 ThemeOf juvenile amyotrophic lateral sclerosis,cause
R7 T5 T3 ThemeOf juvenile primary lateral sclerosis,cause
R8 T12 T11 ThemeOf ALS2,c.1640+1G>A
R9 T11 T10 CauseOf c.1640+1G>A,carrying