http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2482812-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_408a673e5f3674e77d63dfe2a7856215 |
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-156 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6883 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6883 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-09 |
| filingDate | 2003-04-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cacac742723cce6bfce7ae32d198a26d http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b022f3bcb9a4c04ec0a9982e40393c4d http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b8b8c7d800d6f15abaff4c7b8ae6a0e9 |
| publicationDate | 2003-11-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CA-2482812-A1 |
| titleOfInvention | Mitochondrial polymorphisms linked to a predisposition for the development of inappropriate scarring or fibrosis |
| abstract | The present invention relates to an in vitro method for diagnosing or detecting a predisposition to a condition at least partially characterised by inappropriate fibrosis or scarring, the method comprising examining the mitochondrial genome from a subject of interest to detect the presence of a genetic polymorphism or mutation linked to the development of the condition. Regions of the genome that may be examined include the 16srRNA region, the ND2 gene, the cytochrome b (complex III) region and the COI gene. The invention also relates to kits for use in the diagnostic method and the medical use of modulators of the mitochondrial genome. |
| priorityDate | 2002-04-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 71.