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AxD_symptoms  

PMC:3654953 JSONTXT 3 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue hp_id
T1 395-412 Phenotype denotes movement disorder http://purl.obolibrary.org/obo/HP_0100022
T2 418-438 Phenotype denotes cognitive impairment http://purl.obolibrary.org/obo/HP_0100543
T3 1202-1213 Phenotype denotes astrocytoma http://purl.obolibrary.org/obo/HP_0009592
T4 1736-1750 Phenotype denotes leukodystrophy http://purl.obolibrary.org/obo/HP_0002415
T5 2349-2365 Phenotype denotes Rosenthal fibers http://purl.obolibrary.org/obo/HP_0100320
T6 2873-2890 Phenotype denotes movement disorder http://purl.obolibrary.org/obo/HP_0100022
T7 3980-3997 Phenotype denotes neurodegeneration http://purl.obolibrary.org/obo/HP_0002180
T8 4438-4454 Phenotype denotes bipolar disorder http://purl.obolibrary.org/obo/HP_0007302
T9 4460-4470 Phenotype denotes depression http://purl.obolibrary.org/obo/HP_0000716
T10 4576-4582 Phenotype denotes apathy http://purl.obolibrary.org/obo/HP_0000741
T11 4614-4625 Phenotype denotes memory loss http://purl.obolibrary.org/obo/HP_0002354
T12 4665-4676 Phenotype denotes ataxic gait http://purl.obolibrary.org/obo/HP_0002066
T13 4682-4696 Phenotype denotes frequent falls http://purl.obolibrary.org/obo/HP_0002359
T14 4722-4732 Phenotype denotes dysarthria http://purl.obolibrary.org/obo/HP_0001260
T15 4734-4743 Phenotype denotes dysphagia http://purl.obolibrary.org/obo/HP_0002015
T16 4756-4764 Phenotype denotes drooling http://purl.obolibrary.org/obo/HP_0002307
T17 4782-4799 Phenotype denotes palatal myoclonus http://purl.obolibrary.org/obo/HP_0010530
T18 4862-4901 Phenotype denotes abnormalities; visual evoked potentials http://purl.obolibrary.org/obo/HP_0000649
T19 4966-4977 Phenotype denotes ataxic gait http://purl.obolibrary.org/obo/HP_0002066
T20 4995-5005 Phenotype denotes dysarthria http://purl.obolibrary.org/obo/HP_0001260
T21 5007-5024 Phenotype denotes palatal myoclonus http://purl.obolibrary.org/obo/HP_0010530
T22 5030-5039 Phenotype denotes hypotonia http://purl.obolibrary.org/obo/HP_0001290
T23 5094-5107 Phenotype denotes Babinski sign http://purl.obolibrary.org/obo/HP_0003487
T24 5132-5143 Phenotype denotes dyskinesias http://purl.obolibrary.org/obo/HP_0100660
T25 5157-5165 Phenotype denotes dystonia http://purl.obolibrary.org/obo/HP_0001332
T26 5315-5325 Phenotype denotes dysarthria http://purl.obolibrary.org/obo/HP_0001260
T27 5330-5339 Phenotype denotes dysphagia http://purl.obolibrary.org/obo/HP_0002015
T28 5354-5374 Phenotype denotes urinary incontinence http://purl.obolibrary.org/obo/HP_0000020
T29 5765-5777 Phenotype denotes colon cancer http://purl.obolibrary.org/obo/HP_0003003
T30 5869-5875 Phenotype denotes stroke http://purl.obolibrary.org/obo/HP_0001297
T31 5991-6027 Phenotype denotes abnormalities of the pyramidal tract http://purl.obolibrary.org/obo/HP_0002062
T32 7118-7132 Phenotype denotes limb myoclonus http://purl.obolibrary.org/obo/HP_0045084
T33 7182-7202 Phenotype denotes spastic tetraparesis http://purl.obolibrary.org/obo/HP_0001285
T34 7264-7279 Phenotype denotes pes equinovarus http://purl.obolibrary.org/obo/HP_0001762
T35 7308-7321 Phenotype denotes Babinski sign http://purl.obolibrary.org/obo/HP_0003487
T36 7433-7447 Phenotype denotes muscle wasting http://purl.obolibrary.org/obo/HP_0003202
T37 7687-7697 Phenotype denotes hypophonia http://purl.obolibrary.org/obo/HP_0001621
T38 7712-7721 Phenotype denotes dysphagia http://purl.obolibrary.org/obo/HP_0002015
T39 7762-7772 Phenotype denotes spasticity http://purl.obolibrary.org/obo/HP_0001257
T40 7860-7870 Phenotype denotes spasticity http://purl.obolibrary.org/obo/HP_0001257
T41 7898-7910 Phenotype denotes ankle clonus http://purl.obolibrary.org/obo/HP_0011448
T42 8204-8227 Phenotype denotes motor axonal neuropathy http://purl.obolibrary.org/obo/HP_0007002
T43 9087-9107 Phenotype denotes cognitive impairment http://purl.obolibrary.org/obo/HP_0100543
T44 9462-9478 Phenotype denotes leukodystrophies http://purl.obolibrary.org/obo/HP_0002415
T45 9692-9698 Phenotype denotes ataxia http://purl.obolibrary.org/obo/HP_0001251
T46 9703-9723 Phenotype denotes cognitive impairment http://purl.obolibrary.org/obo/HP_0100543
T47 10473-10496 Phenotype denotes motor axonal neuropathy http://purl.obolibrary.org/obo/HP_0007002
T48 10626-10636 Phenotype denotes Dysarthria http://purl.obolibrary.org/obo/HP_0001260
T49 10637-10646 Phenotype denotes dysphagia http://purl.obolibrary.org/obo/HP_0002015
T50 10653-10671 Phenotype denotes Gait abnormalities http://purl.obolibrary.org/obo/HP_0001288
T51 10678-10688 Phenotype denotes Spasticity http://purl.obolibrary.org/obo/HP_0001257
T52 10701-10707 Phenotype denotes Ataxia http://purl.obolibrary.org/obo/HP_0001251
T53 10714-10728 Phenotype denotes Limb dysmetria http://purl.obolibrary.org/obo/HP_0002406
T54 10735-10748 Phenotype denotes Limb weakness http://purl.obolibrary.org/obo/HP_0003690
T55 10755-10769 Phenotype denotes Muscle wasting http://purl.obolibrary.org/obo/HP_0003202
T56 11191-11210 Phenotype denotes social interactions http://purl.obolibrary.org/obo/HP_0008763
T57 17772-17783 Phenotype denotes astrocytoma http://purl.obolibrary.org/obo/HP_0009592
T58 19079-19090 Phenotype denotes astrocytoma http://purl.obolibrary.org/obo/HP_0009592
T59 23126-23143 Phenotype denotes cerebellar ataxia http://purl.obolibrary.org/obo/HP_0001251
T60 23145-23162 Phenotype denotes Palatal myoclonus http://purl.obolibrary.org/obo/HP_0010530
T61 23284-23296 Phenotype denotes dysautonomia http://purl.obolibrary.org/obo/HP_0012332
T62 23530-23550 Phenotype denotes cognitive impairment http://purl.obolibrary.org/obo/HP_0100543
T63 23560-23577 Phenotype denotes movement disorder http://purl.obolibrary.org/obo/HP_0100022
T64 25327-25356 Phenotype denotes amyotrophic lateral sclerosis http://purl.obolibrary.org/obo/HP_0007354
T65 25590-25606 Phenotype denotes muscular atrophy http://purl.obolibrary.org/obo/HP_0003202
T66 25833-25850 Phenotype denotes neurodegeneration http://purl.obolibrary.org/obo/HP_0002180
T67 25976-25993 Phenotype denotes neurodegeneration http://purl.obolibrary.org/obo/HP_0002180
T68 26244-26261 Phenotype denotes neurodegeneration http://purl.obolibrary.org/obo/HP_0002180
T69 26401-26418 Phenotype denotes neurodegeneration http://purl.obolibrary.org/obo/HP_0002180
T70 28950-28968 Phenotype denotes Movement Disorders http://purl.obolibrary.org/obo/HP_0100022
T71 28973-28999 Phenotype denotes Neurodegenerative Diseases http://purl.obolibrary.org/obo/HP_0002180