PubMed:30128655
Annnotations
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 |