http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-03029493-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_adadc7733adc4ea1fc92f8a0f38f3e56 http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_644e7069a5025a929ba9267b3acd9ed1 |
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02A90-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-156 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G16B20-40 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G16H20-30 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G16H20-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6883 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G16B20-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G16B20-00 |
| classificationIPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G16B20-40 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G16B20-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G16H20-30 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G16H20-10 |
| filingDate | 2002-09-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_db0a08f07c1fa22399a27a24baa17dbd |
| publicationDate | 2003-04-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | WO-03029493-A1 |
| titleOfInvention | Diagnosis and treatment of vascular disease |
| abstract | The present invention is based at least in part on the discovery of polymorphisms within the Factor 2 (F2)gene. Accordingly, the invention provides nucleic acid molecules having a nucleotide sequence of an allelic variant of an F2 gene. The invention also provides methods for identifying specific alleles of polymorphic regions of an F2 gene, methods for determining whether a subject has or is at risk of developing a disease which is associated with a specific allele of a polymorphic region of an F2 gene, e.g., a vascular disease, based on detection of one or more polymorphisms within the F2 gene, and kits for performing such methods. The invention further provides methods for identifying a subject who has,or is at risk for developing, a vascular disease or disorder as a candidate for a particular clinical course of therapy or a particular diagnostic evaluation. The invention further provides methods for selecting a clinical course of therapy or a diagnostic evaluation to treat a subject who is at risk for developing,a vascular disease or disorder. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-109300107-A |
| priorityDate | 2001-09-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 224.