PubMed:18305110
Annnotations
PMID_GLOBAL
Id | Subject | Object | Predicate | Lexical cue | mondo_id |
---|---|---|---|---|---|
T1 | 39-42 | DiseaseOrPhenotypicFeature | denotes | TAR | 0010121 |
T2 | 149-152 | DiseaseOrPhenotypicFeature | denotes | TAR | 0010121 |
T3 | 211-244 | DiseaseOrPhenotypicFeature | denotes | frontotemporal lobar degeneration | 0017276 |
T4 | 293-322 | DiseaseOrPhenotypicFeature | denotes | amyotrophic lateral sclerosis | 0004976 |
T5 | 324-327 | DiseaseOrPhenotypicFeature | denotes | ALS | 0004976 |
T6 | 1208-1211 | DiseaseOrPhenotypicFeature | denotes | ALS | 0004976 |
T7 | 1226-1229 | DiseaseOrPhenotypicFeature | denotes | ALS | 0004976 |
sentences
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 0-148 | Sentence | denotes | Disturbance of nuclear and cytoplasmic TAR DNA-binding protein (TDP-43) induces disease-like redistribution, sequestration, and aggregate formation. |
T2 | 149-329 | Sentence | denotes | TAR DNA-binding protein 43 (TDP-43) is the disease protein in frontotemporal lobar degeneration with ubiquitin-positive inclusions (FTLD-U) and amyotrophic lateral sclerosis (ALS). |
T3 | 330-496 | Sentence | denotes | Although normal TDP-43 is a nuclear protein, pathological TDP-43 is redistributed and sequestered as insoluble aggregates in neuronal nuclei, perikarya, and neurites. |
T4 | 497-740 | Sentence | denotes | Here we recapitulate these pathological phenotypes in cultured cells by altering endogenous TDP-43 nuclear trafficking and by expressing mutants with defective nuclear localization (TDP-43-DeltaNLS) or nuclear export signals (TDP-43-DeltaNES). |
T5 | 741-890 | Sentence | denotes | Restricting endogenous cytoplasmic TDP-43 from entering the nucleus or preventing its exit out of the nucleus resulted in TDP-43 aggregate formation. |
T6 | 891-1112 | Sentence | denotes | TDP-43-DeltaNLS accumulates as insoluble cytoplasmic aggregates and sequesters endogenous TDP-43, thereby depleting normal nuclear TDP-43, whereas TDP-43-DeltaNES forms insoluble nuclear aggregates with endogenous TDP-43. |
T7 | 1113-1212 | Sentence | denotes | Mutant forms of TDP-43 also replicate the biochemical profile of pathological TDP-43 in FTLD-U/ALS. |
T8 | 1213-1350 | Sentence | denotes | Thus, FTLD-U/ALS pathogenesis may be linked mechanistically to deleterious perturbations of nuclear trafficking and solubility of TDP-43. |
Glycosmos6-MAT
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 305-312 | http://purl.obolibrary.org/obo/MAT_0000488 | denotes | lateral |
DisGeNET
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T0 | 1343-1349 | gene:23435 | denotes | TDP-43 |
T1 | 1226-1229 | disease:C0002736 | denotes | ALS |
R1 | T0 | T1 | associated_with | TDP-43,ALS |
bionlp-st-epi-2011-training
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 64-70 | Protein | denotes | TDP-43 |
T2 | 149-175 | Protein | denotes | TAR DNA-binding protein 43 |
T3 | 177-183 | Protein | denotes | TDP-43 |
T4 | 250-259 | Protein | denotes | ubiquitin |
T5 | 346-352 | Protein | denotes | TDP-43 |
T6 | 388-394 | Protein | denotes | TDP-43 |
T7 | 589-595 | Protein | denotes | TDP-43 |
T8 | 679-685 | Protein | denotes | TDP-43 |
T9 | 723-729 | Protein | denotes | TDP-43 |
T10 | 776-782 | Protein | denotes | TDP-43 |
T11 | 863-869 | Protein | denotes | TDP-43 |
T12 | 891-897 | Protein | denotes | TDP-43 |
T13 | 981-987 | Protein | denotes | TDP-43 |
T14 | 1022-1028 | Protein | denotes | TDP-43 |
T15 | 1038-1044 | Protein | denotes | TDP-43 |
T16 | 1105-1111 | Protein | denotes | TDP-43 |
T17 | 1129-1135 | Protein | denotes | TDP-43 |
T18 | 1191-1197 | Protein | denotes | TDP-43 |
T19 | 1343-1349 | Protein | denotes | TDP-43 |
DisGeNET5_gene_disease
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
18305110-6#16#22#gene23435 | 1129-1135 | gene23435 | denotes | TDP-43 |
18305110-6#78#84#gene23435 | 1191-1197 | gene23435 | denotes | TDP-43 |
18305110-6#88#94#diseaseC0338451 | 1201-1207 | diseaseC0338451 | denotes | FTLD-U |
18305110-6#88#94#diseaseC1843792 | 1201-1207 | diseaseC1843792 | denotes | FTLD-U |
18305110-6#88#94#diseaseC0338451 | 1201-1207 | diseaseC0338451 | denotes | FTLD-U |
18305110-6#88#94#diseaseC1843792 | 1201-1207 | diseaseC1843792 | denotes | FTLD-U |
18305110-7#130#136#gene23435 | 1343-1349 | gene23435 | denotes | TDP-43 |
18305110-7#13#16#diseaseC0002736 | 1226-1229 | diseaseC0002736 | denotes | ALS |
16#22#gene2343588#94#diseaseC0338451 | 18305110-6#16#22#gene23435 | 18305110-6#88#94#diseaseC0338451 | associated_with | TDP-43,FTLD-U |
16#22#gene2343588#94#diseaseC1843792 | 18305110-6#16#22#gene23435 | 18305110-6#88#94#diseaseC1843792 | associated_with | TDP-43,FTLD-U |
16#22#gene2343588#94#diseaseC0338451 | 18305110-6#16#22#gene23435 | 18305110-6#88#94#diseaseC0338451 | associated_with | TDP-43,FTLD-U |
16#22#gene2343588#94#diseaseC1843792 | 18305110-6#16#22#gene23435 | 18305110-6#88#94#diseaseC1843792 | associated_with | TDP-43,FTLD-U |
78#84#gene2343588#94#diseaseC0338451 | 18305110-6#78#84#gene23435 | 18305110-6#88#94#diseaseC0338451 | associated_with | TDP-43,FTLD-U |
78#84#gene2343588#94#diseaseC1843792 | 18305110-6#78#84#gene23435 | 18305110-6#88#94#diseaseC1843792 | associated_with | TDP-43,FTLD-U |
78#84#gene2343588#94#diseaseC0338451 | 18305110-6#78#84#gene23435 | 18305110-6#88#94#diseaseC0338451 | associated_with | TDP-43,FTLD-U |
78#84#gene2343588#94#diseaseC1843792 | 18305110-6#78#84#gene23435 | 18305110-6#88#94#diseaseC1843792 | associated_with | TDP-43,FTLD-U |
130#136#gene2343513#16#diseaseC0002736 | 18305110-7#130#136#gene23435 | 18305110-7#13#16#diseaseC0002736 | associated_with | TDP-43,ALS |
HP-phenotype
Id | Subject | Object | Predicate | Lexical cue | hp_id |
---|---|---|---|---|---|
T1 | 293-322 | Phenotype | denotes | amyotrophic lateral sclerosis | HP:0007354 |
T2 | 324-327 | Phenotype | denotes | ALS | HP:0007354 |
T3 | 1208-1211 | Phenotype | denotes | ALS | HP:0007354 |
T4 | 1226-1229 | Phenotype | denotes | ALS | HP:0007354 |
mondo_disease
Id | Subject | Object | Predicate | Lexical cue | mondo_id |
---|---|---|---|---|---|
T1 | 39-42 | Disease | denotes | TAR | http://purl.obolibrary.org/obo/MONDO_0010121 |
T2 | 149-152 | Disease | denotes | TAR | http://purl.obolibrary.org/obo/MONDO_0010121 |
T3 | 211-244 | Disease | denotes | frontotemporal lobar degeneration | http://purl.obolibrary.org/obo/MONDO_0017276 |
T4 | 293-322 | Disease | denotes | amyotrophic lateral sclerosis | http://purl.obolibrary.org/obo/MONDO_0004976 |
T5 | 324-327 | Disease | denotes | ALS | http://purl.obolibrary.org/obo/MONDO_0004976 |
T6 | 1208-1211 | Disease | denotes | ALS | http://purl.obolibrary.org/obo/MONDO_0004976 |
T7 | 1226-1229 | Disease | denotes | ALS | http://purl.obolibrary.org/obo/MONDO_0004976 |
Anatomy-UBERON
Id | Subject | Object | Predicate | Lexical cue | uberon_id |
---|---|---|---|---|---|
T1 | 27-38 | Body_part | denotes | cytoplasmic | http://purl.obolibrary.org/obo/GO_0005737 |
T2 | 764-775 | Body_part | denotes | cytoplasmic | http://purl.obolibrary.org/obo/GO_0005737 |
T3 | 801-808 | Body_part | denotes | nucleus | http://purl.obolibrary.org/obo/GO_0005634|http://purl.obolibrary.org/obo/UBERON_0000125 |
T5 | 843-850 | Body_part | denotes | nucleus | http://purl.obolibrary.org/obo/GO_0005634|http://purl.obolibrary.org/obo/UBERON_0000125 |
T7 | 932-943 | Body_part | denotes | cytoplasmic | http://purl.obolibrary.org/obo/GO_0005737 |
Anatomy-MAT
Id | Subject | Object | Predicate | Lexical cue | mat_id |
---|---|---|---|---|---|
T1 | 305-312 | Body_part | denotes | lateral | http://purl.obolibrary.org/obo/MAT_0000488 |
CL-cell
Id | Subject | Object | Predicate | Lexical cue | cl_id |
---|---|---|---|---|---|
T1 | 455-463 | Cell | denotes | neuronal | http://purl.obolibrary.org/obo/CL:0000540 |
T2 | 551-565 | Cell | denotes | cultured cells | http://purl.obolibrary.org/obo/CL:0000010 |