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sonoma

Id Subject Object Predicate Lexical cue
T0 0-18 DISEASE denotes Motor neuropathies
T1 23-51 DISEASE denotes lower motor neuron syndromes
T2 53-92 DISEASE denotes Motor or motor-predominant neuropathies
T3 97-102 REG denotes arise
T4 126-135 REG denotes affecting
T5 140-150 CPA denotes motor axon
T6 182-209 DISEASE denotes Lower motor neuron syndrome
T7 211-215 DISEASE denotes LMNS
T8 217-223 REG denotes arises
T9 247-256 REG denotes affecting
T10 298-302 DISEASE denotes LMNS
T11 339-357 DISEASE denotes motor neuronopathy
T12 397-404 REG denotes similar
T13 426-441 CPA denotes muscle weakness
T14 468-475 CPA denotes atrophy
T15 480-492 CPA denotes hyporeflexia
T16 501-520 CPA denotes sensory involvement
T17 558-586 DISEASE denotes Immune-mediated neuropathies
T18 588-615 DISEASE denotes multifocal motor neuropathy
T19 617-684 DISEASE denotes motor-predominant chronic inflammatory demyelinating polyneuropathy
T20 767-779 DISEASE denotes neuropathies
T21 820-850 DISEASE denotes radiation-induced neuropathies
T22 865-870 REG denotes known
T23 872-882 DISEASE denotes Focal LMNS
T24 889-943 DISEASE denotes amyotrophic lateral sclerosis (ALS)-mimicking syndrome
T25 955-964 REG denotes affecting
T26 999-1004 DISEASE denotes LMNSs
T27 1022-1039 DISEASE denotes Kennedy's disease
T28 1041-1075 DISEASE denotes late-onset spinal muscular atrophy
T29 1080-1116 DISEASE denotes distal hereditary motor neuropathies
T30 1118-1136 DISEASE denotes Motor neuropathies
T31 1141-1145 DISEASE denotes LMNS
T32 1280-1288 REG denotes diagnose
T33 1337-1345 REG denotes frequent
T34 1346-1349 DISEASE denotes ALS
T35 1362-1365 DISEASE denotes LMN
T36 1494-1503 REG denotes different
R0 T2 T3 ThemeOf Motor or motor-predominant neuropathies,arise
R1 T2 T4 ThemeOf Motor or motor-predominant neuropathies,affecting
R2 T5 T4 ThemeOf motor axon,affecting
R3 T6 T8 ThemeOf Lower motor neuron syndrome,arises
R4 T6 T9 ThemeOf Lower motor neuron syndrome,affecting
R5 T7 T8 ThemeOf LMNS,arises
R6 T7 T9 ThemeOf LMNS,affecting
R7 T10 T12 ThemeOf LMNS,similar
R8 T11 T12 ThemeOf motor neuronopathy,similar
R9 T20 T22 ThemeOf neuropathies,known
R10 T21 T22 ThemeOf radiation-induced neuropathies,known
R11 T23 T25 ThemeOf Focal LMNS,affecting
R12 T24 T25 ThemeOf amyotrophic lateral sclerosis (ALS)-mimicking syndrome,affecting
R13 T34 T32 ThemeOf ALS,diagnose
R14 T34 T33 ThemeOf ALS,frequent
R15 T35 T32 ThemeOf LMN,diagnose
R16 T35 T33 ThemeOf LMN,frequent

Inflammaging

Id Subject Object Predicate Lexical cue
T1 0-52 Sentence denotes Motor neuropathies and lower motor neuron syndromes.
T2 53-181 Sentence denotes Motor or motor-predominant neuropathies may arise from disease processes affecting the motor axon and/or its surrounding myelin.
T3 182-288 Sentence denotes Lower motor neuron syndrome (LMNS) arises from a disease process affecting the spinal motor neuron itself.
T4 289-405 Sentence denotes The term LMNS is more generally used, rather than motor neuronopathy, although both entities are clinically similar.
T5 406-521 Sentence denotes Common features are muscle weakness (distal or proximal) with atrophy and hyporeflexia, but no sensory involvement.
T6 522-557 Sentence denotes They can be acquired or hereditary.
T7 558-751 Sentence denotes Immune-mediated neuropathies (multifocal motor neuropathy, motor-predominant chronic inflammatory demyelinating polyneuropathy) are important to identify, as effective treatments are available.
T8 752-871 Sentence denotes Other acquired neuropathies, such as infectious, paraneoplastic and radiation-induced neuropathies are also well known.
T9 872-978 Sentence denotes Focal LMNS is an amyotrophic lateral sclerosis (ALS)-mimicking syndrome especially affecting young adults.
T10 979-1117 Sentence denotes The main hereditary LMNSs in adulthood are Kennedy's disease, late-onset spinal muscular atrophy and distal hereditary motor neuropathies.
T11 1118-1229 Sentence denotes Motor neuropathies and LMNS are all clinical entities that should be better known, despite being rare diseases.
T12 1230-1371 Sentence denotes They can sometimes be difficult to differentially diagnose from other diseases, particularly from the more frequent ALS in its pure LMN form.
T13 1372-1504 Sentence denotes Nevertheless, correct identification of these syndromes is important because their treatment and prognoses are definitely different.
T1 0-52 Sentence denotes Motor neuropathies and lower motor neuron syndromes.
T2 53-181 Sentence denotes Motor or motor-predominant neuropathies may arise from disease processes affecting the motor axon and/or its surrounding myelin.
T3 182-288 Sentence denotes Lower motor neuron syndrome (LMNS) arises from a disease process affecting the spinal motor neuron itself.
T4 289-405 Sentence denotes The term LMNS is more generally used, rather than motor neuronopathy, although both entities are clinically similar.
T5 406-521 Sentence denotes Common features are muscle weakness (distal or proximal) with atrophy and hyporeflexia, but no sensory involvement.
T6 522-557 Sentence denotes They can be acquired or hereditary.
T7 558-751 Sentence denotes Immune-mediated neuropathies (multifocal motor neuropathy, motor-predominant chronic inflammatory demyelinating polyneuropathy) are important to identify, as effective treatments are available.
T8 752-871 Sentence denotes Other acquired neuropathies, such as infectious, paraneoplastic and radiation-induced neuropathies are also well known.
T9 872-978 Sentence denotes Focal LMNS is an amyotrophic lateral sclerosis (ALS)-mimicking syndrome especially affecting young adults.
T10 979-1117 Sentence denotes The main hereditary LMNSs in adulthood are Kennedy's disease, late-onset spinal muscular atrophy and distal hereditary motor neuropathies.
T11 1118-1229 Sentence denotes Motor neuropathies and LMNS are all clinical entities that should be better known, despite being rare diseases.
T12 1230-1371 Sentence denotes They can sometimes be difficult to differentially diagnose from other diseases, particularly from the more frequent ALS in its pure LMN form.
T13 1372-1504 Sentence denotes Nevertheless, correct identification of these syndromes is important because their treatment and prognoses are definitely different.