PubMed:22166430
Annnotations
c_corpus
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 0-5 | 10090 | denotes | Mouse |
| T2 | 0-5 | D051379 | denotes | Mouse |
| T3 | 17-22 | PR:Q5S006 | denotes | LRRK2 |
| T4 | 17-22 | PR:000003033 | denotes | LRRK2 |
| T5 | 17-22 | PR:Q5S007 | denotes | LRRK2 |
| T10 | 23-42 | D010300 | denotes | Parkinson's disease |
| T11 | 23-42 | D010300 | denotes | Parkinson's disease |
| T14 | 56-63 | D004194 | denotes | disease |
| T15 | 56-63 | D004194 | denotes | disease |
| T18 | 95-120 | D019636 | denotes | neurodegenerative disease |
| T19 | 95-120 | D019636 | denotes | neurodegenerative disease |
| T23 | 135-142 | 6308 | denotes | Leucine |
| T24 | 135-142 | SO:0001437 | denotes | Leucine |
| T22 | 135-142 | CHEBI:15603 | denotes | Leucine |
| T25 | 135-142 | D007930 | denotes | Leucine |
| T26 | 135-142 | CHEBI:25017 | denotes | Leucine |
| T27 | 135-142 | D007930 | denotes | Leucine |
| T28 | 148-154 | SO:0001068 | denotes | repeat |
| T29 | 165-170 | PR:Q5S006 | denotes | LRRK2 |
| T30 | 165-170 | PR:000003033 | denotes | LRRK2 |
| T31 | 165-170 | PR:Q5S007 | denotes | LRRK2 |
| T32 | 187-191 | SO:0000704 | denotes | gene |
| T35 | 196-201 | PR:000003033 | denotes | PARK8 |
| T36 | 196-201 | PR:Q5S007 | denotes | PARK8 |
| T34 | 196-201 | 607060 | denotes | PARK8 |
| T37 | 215-233 | C566739 | denotes | autosomal dominant |
| T38 | 319-325 | D000818 | denotes | Animal |
| T39 | 399-404 | PR:Q5S006 | denotes | LRRK2 |
| T40 | 399-404 | PR:000003033 | denotes | LRRK2 |
| T41 | 399-404 | PR:Q5S007 | denotes | LRRK2 |
| T42 | 414-426 | GO:0009405 | denotes | pathogenesis |
| T43 | 446-451 | D006801 | denotes | human |
| T44 | 452-483 | SO:0000153 | denotes | Bacterial Artificial Chromosome |
| T45 | 473-483 | GO:0005694 | denotes | Chromosome |
| T47 | 485-488 | SO:0000153 | denotes | BAC |
| T48 | 499-509 | SO:0000781 | denotes | transgenic |
| T49 | 499-515 | D008822 | denotes | transgenic mouse |
| T52 | 541-546 | PR:Q5S006 | denotes | LRRK2 |
| T53 | 541-546 | PR:000003033 | denotes | LRRK2 |
| T54 | 541-546 | PR:Q5S007 | denotes | LRRK2 |
| T55 | 643-647 | PR:000005054 | denotes | mice |
| T57 | 643-647 | O89094 | denotes | mice |
| T56 | 643-647 | D051379 | denotes | mice |
| T58 | 643-647 | 10095 | denotes | mice |
| T59 | 685-699 | GO:0003774 | denotes | motor activity |
| T61 | 751-759 | 6375 | denotes | levodopa |
| T60 | 751-759 | D007980 | denotes | levodopa |
| T62 | 751-759 | CHEBI:15765 | denotes | levodopa |
| T63 | 751-759 | D007980 | denotes | levodopa |
| T64 | 898-901 | PR:P16525 | denotes | tau |
| T65 | 898-901 | PR:000024142 | denotes | tau |
| T66 | 898-901 | PR:P10636 | denotes | tau |
| T67 | 898-901 | PR:000010173 | denotes | tau |
| T68 | 898-901 | PR:P19332 | denotes | tau |
| T70 | 898-901 | PR:P10637 | denotes | tau |
| T69 | 898-901 | CHEBI:36355 | denotes | tau |
| T71 | 907-911 | PR:000005054 | denotes | mice |
| T73 | 907-911 | O89094 | denotes | mice |
| T72 | 907-911 | D051379 | denotes | mice |
| T74 | 907-911 | 10095 | denotes | mice |
| T75 | 938-946 | CHEBI:59905 | denotes | dopamine |
| T76 | 938-946 | CHEBI:18243 | denotes | dopamine |
| T77 | 938-946 | D004298 | denotes | dopamine |
| T78 | 938-946 | D004298 | denotes | dopamine |
| T79 | 938-946 | 3628 | denotes | dopamine |
| T80 | 982-987 | UBERON:6110636 | denotes | brain |
| T81 | 982-987 | UBERON:0000955 | denotes | brain |
| T85 | 1048-1059 | MGI:1913975 | denotes | LRRK2 mouse |
| T86 | 1054-1059 | 10090 | denotes | mouse |
| T87 | 1054-1059 | D051379 | denotes | mouse |
Allie
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| SS1_22166430_1_0 | 44-63 | expanded | denotes | Parkinson's disease |
| SS2_22166430_1_0 | 65-67 | abbr | denotes | PD |
| SS1_22166430_2_0 | 135-163 | expanded | denotes | Leucine-rich-repeat-kinase 2 |
| SS2_22166430_2_0 | 165-170 | abbr | denotes | LRRK2 |
| SS1_22166430_4_0 | 452-483 | expanded | denotes | Bacterial Artificial Chromosome |
| SS2_22166430_4_0 | 485-488 | abbr | denotes | BAC |
| AE1_22166430_1_0 | SS1_22166430_1_0 | SS2_22166430_1_0 | abbreviatedTo | Parkinson's disease,PD |
| AE1_22166430_2_0 | SS1_22166430_2_0 | SS2_22166430_2_0 | abbreviatedTo | Leucine-rich-repeat-kinase 2,LRRK2 |
| AE1_22166430_4_0 | SS1_22166430_4_0 | SS2_22166430_4_0 | abbreviatedTo | Bacterial Artificial Chromosome,BAC |
PubMed_ArguminSci
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 44-121 | DRI_Background | denotes | Parkinson's disease (PD) is the second most common neurodegenerative disease. |
| T2 | 122-318 | DRI_Outcome | denotes | Mutations in Leucine-rich-repeat-kinase 2 (LRRK2), the causative gene for PARK8 type PD with autosomal dominant inheritance, are the most prevalent genetic causes of both familial and sporadic PD. |
| T3 | 319-427 | DRI_Background | denotes | Animal models are critical tools in the attempt to understand the mechanisms of LRRK2-mediated pathogenesis. |
| T4 | 428-636 | DRI_Outcome | denotes | We have generated human Bacterial Artificial Chromosome (BAC) mediated transgenic mouse models expressing mutant LRRK2 that robustly recapitulate the behavioral, neurochemical and pathological features of PD. |
| T5 | 637-760 | DRI_Background | denotes | These mice develop an age-dependent decrease in motor activity that is progressive and responds to treatment with levodopa. |
| T6 | 761-902 | DRI_Background | denotes | Pathologically, the most salient phenotype is early axonopathy of nigrostriatal dopaminergic neurons, accompanied by hyperphosphorylated tau. |
| T7 | 903-1026 | DRI_Outcome | denotes | The mice also exhibit a consistent dopamine transmission deficit in both acute brain slices and live freely moving animals. |
| T8 | 1027-1186 | DRI_Outcome | denotes | Here we will discuss LRRK2 mouse models from several laboratories, their commonalities and differences, and offer scientific insights drawn from these studies. |
PubmedHPO
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 44-53 | HP_0001300 | denotes | Parkinson |
| T2 | 215-245 | HP_0000006 | denotes | autosomal dominant inheritance |
| T3 | 215-233 | HP_0000006 | denotes | autosomal dominant |
DisGeNET5_gene_disease
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| 22166430-0#17#22#gene120892 | 17-22 | gene120892 | denotes | LRRK2 |
| 22166430-0#23#42#diseaseC0030567 | 23-42 | diseaseC0030567 | denotes | Parkinson's disease |
| 17#22#gene12089223#42#diseaseC0030567 | 22166430-0#17#22#gene120892 | 22166430-0#23#42#diseaseC0030567 | associated_with | LRRK2,Parkinson's disease |