PubMed:15122708
Annnotations
TEST-CellLine
| Id | Subject | Object | Predicate | Lexical cue | cellosaurus_accession_id |
|---|---|---|---|---|---|
| T1 | 357-360 | CellLine | denotes | DRM | CVCL_1G81 |
| T2 | 976-979 | CellLine | denotes | DRM | CVCL_1G81 |
| T3 | 1010-1013 | CellLine | denotes | DRM | CVCL_1G81 |
| T4 | 1238-1241 | CellLine | denotes | DRM | CVCL_1G81 |
| T5 | 1319-1322 | CellLine | denotes | DRM | CVCL_1G81 |
| T6 | 1416-1419 | CellLine | denotes | DRM | CVCL_1G81 |
TEST-DiseaseOrPhenotypicFeature
| Id | Subject | Object | Predicate | Lexical cue | #label |
|---|---|---|---|---|---|
| T1 | 0-41 | DiseaseOrPhenotypicFeature | denotes | Desmin-related myopathy with Mallory body | C535683 |
| T2 | 110-135 | DiseaseOrPhenotypicFeature | denotes | Desmin-related myopathies | C563319 |
| T3 | 137-141 | DiseaseOrPhenotypicFeature | denotes | DRMs | C563319 |
| T4 | 172-188 | DiseaseOrPhenotypicFeature | denotes | muscle disorders | D009135 |
| T5 | 498-500 | DiseaseOrPhenotypicFeature | denotes | MB | DISEASE |
| T6 | 501-505 | DiseaseOrPhenotypicFeature | denotes | DRMs | C563319 |
| T7 | 646-654 | DiseaseOrPhenotypicFeature | denotes | myopathy | D009135 |
| T8 | 687-695 | DiseaseOrPhenotypicFeature | denotes | myopathy | D009135 |
| T9 | 766-784 | DiseaseOrPhenotypicFeature | denotes | muscular dystrophy | D009136 |
| T10 | 818-839 | DiseaseOrPhenotypicFeature | denotes | multiminicore disease | C564969 |
| T11 | 973-975 | DiseaseOrPhenotypicFeature | denotes | MB | DISEASE |
| T12 | 1007-1009 | DiseaseOrPhenotypicFeature | denotes | MB | DISEASE |
| T13 | 1235-1237 | DiseaseOrPhenotypicFeature | denotes | MB | DISEASE |
| T14 | 1316-1318 | DiseaseOrPhenotypicFeature | denotes | MB | DISEASE |
| T15 | 1551-1561 | DiseaseOrPhenotypicFeature | denotes | myopathies | D009135 |
TEST-ChemicalEntity
| Id | Subject | Object | Predicate | Lexical cue | ID: |
|---|---|---|---|---|---|
| T1 | 88-101 | ChemicalEntity | denotes | selenoprotein | http://purl.obolibrary.org/obo/CHEBI_80757 |
| T2 | 585-598 | ChemicalEntity | denotes | selenoprotein | http://purl.obolibrary.org/obo/CHEBI_80757 |
TEST-OrganismTaxon
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 547-555 | OrganismTaxon | denotes | patients |
| T2 | 1186-1194 | OrganismTaxon | denotes | patients |
Test-GeneOrGeneProduct
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 0-6 | GeneOrGeneProduct | denotes | Desmin |
| T2 | 88-103 | GeneOrGeneProduct | denotes | selenoprotein N |
| T3 | 110-116 | GeneOrGeneProduct | denotes | Desmin |
| T4 | 249-255 | GeneOrGeneProduct | denotes | desmin |
| T5 | 274-280 | GeneOrGeneProduct | denotes | desmin |
| T6 | 289-307 | GeneOrGeneProduct | denotes | alpha-B crystallin |
| T7 | 585-600 | GeneOrGeneProduct | denotes | selenoprotein N |
| T8 | 607-612 | GeneOrGeneProduct | denotes | SEPN1 |
| T9 | 984-989 | GeneOrGeneProduct | denotes | SEPN1 |
| T10 | 1077-1082 | GeneOrGeneProduct | denotes | SEPN1 |
| T11 | 1127-1132 | GeneOrGeneProduct | denotes | SEPN1 |
Test-merged-2
| Id | Subject | Object | Predicate | Lexical cue | #label | ID: | cellosaurus_accession_id |
|---|---|---|---|---|---|---|---|
| T77232 | 357-360 | CellLine | denotes | DRM | CVCL_1G81 | ||
| T85636 | 976-979 | CellLine | denotes | DRM | CVCL_1G81 | ||
| T2801 | 1010-1013 | CellLine | denotes | DRM | CVCL_1G81 | ||
| T87186 | 1238-1241 | CellLine | denotes | DRM | CVCL_1G81 | ||
| T24812 | 1319-1322 | CellLine | denotes | DRM | CVCL_1G81 | ||
| T84250 | 1416-1419 | CellLine | denotes | DRM | CVCL_1G81 | ||
| T56406 | 88-101 | ChemicalEntity | denotes | selenoprotein | http://purl.obolibrary.org/obo/CHEBI_80757 | ||
| T33937 | 585-598 | ChemicalEntity | denotes | selenoprotein | http://purl.obolibrary.org/obo/CHEBI_80757 | ||
| T87659 | 0-6 | GeneOrGeneProduct | denotes | Desmin | |||
| T66366 | 88-103 | GeneOrGeneProduct | denotes | selenoprotein N | |||
| T22768 | 110-116 | GeneOrGeneProduct | denotes | Desmin | |||
| T82381 | 249-255 | GeneOrGeneProduct | denotes | desmin | |||
| T38213 | 274-280 | GeneOrGeneProduct | denotes | desmin | |||
| T68109 | 289-307 | GeneOrGeneProduct | denotes | alpha-B crystallin | |||
| T17249 | 585-600 | GeneOrGeneProduct | denotes | selenoprotein N | |||
| T31521 | 607-612 | GeneOrGeneProduct | denotes | SEPN1 | |||
| T14435 | 984-989 | GeneOrGeneProduct | denotes | SEPN1 | |||
| T96348 | 1077-1082 | GeneOrGeneProduct | denotes | SEPN1 | |||
| T52223 | 1127-1132 | GeneOrGeneProduct | denotes | SEPN1 | |||
| T22421 | 547-555 | OrganismTaxon | denotes | patients | |||
| T80174 | 1186-1194 | OrganismTaxon | denotes | patients | |||
| T1 | 0-41 | DiseaseOrPhenotypicFeature | denotes | Desmin-related myopathy with Mallory body | C535683 | ||
| T2 | 110-135 | DiseaseOrPhenotypicFeature | denotes | Desmin-related myopathies | C563319 | ||
| T3 | 137-141 | DiseaseOrPhenotypicFeature | denotes | DRMs | C563319 | ||
| T4 | 172-188 | DiseaseOrPhenotypicFeature | denotes | muscle disorders | D009135 | ||
| T5 | 498-500 | DiseaseOrPhenotypicFeature | denotes | MB | DISEASE | ||
| T6 | 501-505 | DiseaseOrPhenotypicFeature | denotes | DRMs | C563319 | ||
| T7 | 646-654 | DiseaseOrPhenotypicFeature | denotes | myopathy | D009135 | ||
| T8 | 687-695 | DiseaseOrPhenotypicFeature | denotes | myopathy | D009135 | ||
| T9 | 766-784 | DiseaseOrPhenotypicFeature | denotes | muscular dystrophy | D009136 | ||
| T10 | 818-839 | DiseaseOrPhenotypicFeature | denotes | multiminicore disease | C564969 | ||
| T11 | 973-975 | DiseaseOrPhenotypicFeature | denotes | MB | DISEASE | ||
| T12 | 1007-1009 | DiseaseOrPhenotypicFeature | denotes | MB | DISEASE | ||
| T13 | 1235-1237 | DiseaseOrPhenotypicFeature | denotes | MB | DISEASE | ||
| T14 | 1316-1318 | DiseaseOrPhenotypicFeature | denotes | MB | DISEASE | ||
| T15 | 1551-1561 | DiseaseOrPhenotypicFeature | denotes | myopathies | D009135 |
Test-merged
| Id | Subject | Object | Predicate | Lexical cue | #label | cellosaurus_accession_id |
|---|---|---|---|---|---|---|
| T15 | 1551-1561 | DiseaseOrPhenotypicFeature | denotes | myopathies | D009135 | |
| T14 | 1316-1318 | DiseaseOrPhenotypicFeature | denotes | MB | DISEASE | |
| T13 | 1235-1237 | DiseaseOrPhenotypicFeature | denotes | MB | DISEASE | |
| T12 | 1007-1009 | DiseaseOrPhenotypicFeature | denotes | MB | DISEASE | |
| T11 | 973-975 | DiseaseOrPhenotypicFeature | denotes | MB | DISEASE | |
| T10 | 818-839 | DiseaseOrPhenotypicFeature | denotes | multiminicore disease | C564969 | |
| T9 | 766-784 | DiseaseOrPhenotypicFeature | denotes | muscular dystrophy | D009136 | |
| T8 | 687-695 | DiseaseOrPhenotypicFeature | denotes | myopathy | D009135 | |
| T7 | 646-654 | DiseaseOrPhenotypicFeature | denotes | myopathy | D009135 | |
| T6 | 501-505 | DiseaseOrPhenotypicFeature | denotes | DRMs | C563319 | |
| T5 | 498-500 | DiseaseOrPhenotypicFeature | denotes | MB | DISEASE | |
| T4 | 172-188 | DiseaseOrPhenotypicFeature | denotes | muscle disorders | D009135 | |
| T3 | 137-141 | DiseaseOrPhenotypicFeature | denotes | DRMs | C563319 | |
| T2 | 110-135 | DiseaseOrPhenotypicFeature | denotes | Desmin-related myopathies | C563319 | |
| T1 | 0-41 | DiseaseOrPhenotypicFeature | denotes | Desmin-related myopathy with Mallory body | C535683 | |
| T80174 | 1186-1194 | OrganismTaxon | denotes | patients | ||
| T22421 | 547-555 | OrganismTaxon | denotes | patients | ||
| T52223 | 1127-1132 | GeneOrGeneProduct | denotes | SEPN1 | ||
| T96348 | 1077-1082 | GeneOrGeneProduct | denotes | SEPN1 | ||
| T14435 | 984-989 | GeneOrGeneProduct | denotes | SEPN1 | ||
| T31521 | 607-612 | GeneOrGeneProduct | denotes | SEPN1 | ||
| T17249 | 585-600 | GeneOrGeneProduct | denotes | selenoprotein N | ||
| T68109 | 289-307 | GeneOrGeneProduct | denotes | alpha-B crystallin | ||
| T38213 | 274-280 | GeneOrGeneProduct | denotes | desmin | ||
| T82381 | 249-255 | GeneOrGeneProduct | denotes | desmin | ||
| T66366 | 88-103 | GeneOrGeneProduct | denotes | selenoprotein N | ||
| T84250 | 1416-1419 | CellLine | denotes | DRM | CVCL_1G81 | |
| T24812 | 1319-1322 | CellLine | denotes | DRM | CVCL_1G81 | |
| T87186 | 1238-1241 | CellLine | denotes | DRM | CVCL_1G81 | |
| T2801 | 1010-1013 | CellLine | denotes | DRM | CVCL_1G81 | |
| T85636 | 976-979 | CellLine | denotes | DRM | CVCL_1G81 | |
| T77232 | 357-360 | CellLine | denotes | DRM | CVCL_1G81 |
DisGeNET5_gene_disease
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| 15122708-1#0#6#gene1674 | 110-116 | gene1674 | denotes | Desmin |
| 15122708-1#62#78#diseaseC0026848 | 172-188 | diseaseC0026848 | denotes | muscle disorders |
| 15122708-4#28#43#gene57190 | 585-600 | gene57190 | denotes | selenoprotein N |
| 15122708-4#50#55#gene57190 | 607-612 | gene57190 | denotes | SEPN1 |
| 15122708-4#28#43#gene57190 | 585-600 | gene57190 | denotes | selenoprotein N |
| 15122708-4#50#55#gene57190 | 607-612 | gene57190 | denotes | SEPN1 |
| 15122708-4#261#282#diseaseC0270962 | 818-839 | diseaseC0270962 | denotes | multiminicore disease |
| 15122708-4#261#282#diseaseC1850674 | 818-839 | diseaseC1850674 | denotes | multiminicore disease |
| 15122708-4#261#282#diseaseC0270962 | 818-839 | diseaseC0270962 | denotes | multiminicore disease |
| 15122708-4#261#282#diseaseC1850674 | 818-839 | diseaseC1850674 | denotes | multiminicore disease |
| 15122708-4#130#138#diseaseC0026848 | 687-695 | diseaseC0026848 | denotes | myopathy |
| 15122708-4#209#227#diseaseC0026850 | 766-784 | diseaseC0026850 | denotes | muscular dystrophy |
| 15122708-4#130#138#diseaseC0026848 | 687-695 | diseaseC0026848 | denotes | myopathy |
| 15122708-4#209#227#diseaseC0026850 | 766-784 | diseaseC0026850 | denotes | muscular dystrophy |
| 0#6#gene167462#78#diseaseC0026848 | 15122708-1#0#6#gene1674 | 15122708-1#62#78#diseaseC0026848 | associated_with | Desmin,muscle disorders |
| 28#43#gene57190261#282#diseaseC0270962 | 15122708-4#28#43#gene57190 | 15122708-4#261#282#diseaseC0270962 | associated_with | selenoprotein N,multiminicore disease |
| 28#43#gene57190261#282#diseaseC1850674 | 15122708-4#28#43#gene57190 | 15122708-4#261#282#diseaseC1850674 | associated_with | selenoprotein N,multiminicore disease |
| 28#43#gene57190261#282#diseaseC0270962 | 15122708-4#28#43#gene57190 | 15122708-4#261#282#diseaseC0270962 | associated_with | selenoprotein N,multiminicore disease |
| 28#43#gene57190261#282#diseaseC1850674 | 15122708-4#28#43#gene57190 | 15122708-4#261#282#diseaseC1850674 | associated_with | selenoprotein N,multiminicore disease |
| 28#43#gene57190130#138#diseaseC0026848 | 15122708-4#28#43#gene57190 | 15122708-4#130#138#diseaseC0026848 | associated_with | selenoprotein N,myopathy |
| 28#43#gene57190209#227#diseaseC0026850 | 15122708-4#28#43#gene57190 | 15122708-4#209#227#diseaseC0026850 | associated_with | selenoprotein N,muscular dystrophy |
| 28#43#gene57190130#138#diseaseC0026848 | 15122708-4#28#43#gene57190 | 15122708-4#130#138#diseaseC0026848 | associated_with | selenoprotein N,myopathy |
| 28#43#gene57190209#227#diseaseC0026850 | 15122708-4#28#43#gene57190 | 15122708-4#209#227#diseaseC0026850 | associated_with | selenoprotein N,muscular dystrophy |
| 50#55#gene57190261#282#diseaseC0270962 | 15122708-4#50#55#gene57190 | 15122708-4#261#282#diseaseC0270962 | associated_with | SEPN1,multiminicore disease |
| 50#55#gene57190261#282#diseaseC1850674 | 15122708-4#50#55#gene57190 | 15122708-4#261#282#diseaseC1850674 | associated_with | SEPN1,multiminicore disease |
| 50#55#gene57190261#282#diseaseC0270962 | 15122708-4#50#55#gene57190 | 15122708-4#261#282#diseaseC0270962 | associated_with | SEPN1,multiminicore disease |
| 50#55#gene57190261#282#diseaseC1850674 | 15122708-4#50#55#gene57190 | 15122708-4#261#282#diseaseC1850674 | associated_with | SEPN1,multiminicore disease |
| 50#55#gene57190130#138#diseaseC0026848 | 15122708-4#50#55#gene57190 | 15122708-4#130#138#diseaseC0026848 | associated_with | SEPN1,myopathy |
| 50#55#gene57190209#227#diseaseC0026850 | 15122708-4#50#55#gene57190 | 15122708-4#209#227#diseaseC0026850 | associated_with | SEPN1,muscular dystrophy |
| 50#55#gene57190130#138#diseaseC0026848 | 15122708-4#50#55#gene57190 | 15122708-4#130#138#diseaseC0026848 | associated_with | SEPN1,myopathy |
| 50#55#gene57190209#227#diseaseC0026850 | 15122708-4#50#55#gene57190 | 15122708-4#209#227#diseaseC0026850 | associated_with | SEPN1,muscular dystrophy |
| 28#43#gene57190261#282#diseaseC0270962 | 15122708-4#28#43#gene57190 | 15122708-4#261#282#diseaseC0270962 | associated_with | selenoprotein N,multiminicore disease |
| 28#43#gene57190261#282#diseaseC1850674 | 15122708-4#28#43#gene57190 | 15122708-4#261#282#diseaseC1850674 | associated_with | selenoprotein N,multiminicore disease |
| 28#43#gene57190261#282#diseaseC0270962 | 15122708-4#28#43#gene57190 | 15122708-4#261#282#diseaseC0270962 | associated_with | selenoprotein N,multiminicore disease |
| 28#43#gene57190261#282#diseaseC1850674 | 15122708-4#28#43#gene57190 | 15122708-4#261#282#diseaseC1850674 | associated_with | selenoprotein N,multiminicore disease |
| 28#43#gene57190130#138#diseaseC0026848 | 15122708-4#28#43#gene57190 | 15122708-4#130#138#diseaseC0026848 | associated_with | selenoprotein N,myopathy |
| 28#43#gene57190209#227#diseaseC0026850 | 15122708-4#28#43#gene57190 | 15122708-4#209#227#diseaseC0026850 | associated_with | selenoprotein N,muscular dystrophy |
| 28#43#gene57190130#138#diseaseC0026848 | 15122708-4#28#43#gene57190 | 15122708-4#130#138#diseaseC0026848 | associated_with | selenoprotein N,myopathy |
| 28#43#gene57190209#227#diseaseC0026850 | 15122708-4#28#43#gene57190 | 15122708-4#209#227#diseaseC0026850 | associated_with | selenoprotein N,muscular dystrophy |
| 50#55#gene57190261#282#diseaseC0270962 | 15122708-4#50#55#gene57190 | 15122708-4#261#282#diseaseC0270962 | associated_with | SEPN1,multiminicore disease |
| 50#55#gene57190261#282#diseaseC1850674 | 15122708-4#50#55#gene57190 | 15122708-4#261#282#diseaseC1850674 | associated_with | SEPN1,multiminicore disease |
| 50#55#gene57190261#282#diseaseC0270962 | 15122708-4#50#55#gene57190 | 15122708-4#261#282#diseaseC0270962 | associated_with | SEPN1,multiminicore disease |
| 50#55#gene57190261#282#diseaseC1850674 | 15122708-4#50#55#gene57190 | 15122708-4#261#282#diseaseC1850674 | associated_with | SEPN1,multiminicore disease |
| 50#55#gene57190130#138#diseaseC0026848 | 15122708-4#50#55#gene57190 | 15122708-4#130#138#diseaseC0026848 | associated_with | SEPN1,myopathy |
| 50#55#gene57190209#227#diseaseC0026850 | 15122708-4#50#55#gene57190 | 15122708-4#209#227#diseaseC0026850 | associated_with | SEPN1,muscular dystrophy |
| 50#55#gene57190130#138#diseaseC0026848 | 15122708-4#50#55#gene57190 | 15122708-4#130#138#diseaseC0026848 | associated_with | SEPN1,myopathy |
| 50#55#gene57190209#227#diseaseC0026850 | 15122708-4#50#55#gene57190 | 15122708-4#209#227#diseaseC0026850 | associated_with | SEPN1,muscular dystrophy |
tmVarCorpus
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 1143-1168 | DNAMutation:c|DEL|-19_+73|92 | denotes | del 92 nucleotide -19/+73 |
DisGeNET
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T0 | 110-116 | gene:1674 | denotes | Desmin |
| T1 | 172-188 | disease:C0026848 | denotes | muscle disorders |
| R1 | T0 | T1 | associated_with | Desmin,muscle disorders |