| Predicate |
Object |
| assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_43a72884e25aaecffebe0942132d704f |
| classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-156
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-172 |
| classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6883 |
| classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68 |
| filingDate |
2004-12-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4793d46c4ce2a76e9421111e74928f11
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0ecde84094a434726e4d54100c9c61e7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b469b86e0a804723e57c62e4181bbfa8
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_69c4d6223c48025d8ac26cea12db5faa |
| publicationDate |
2006-06-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber |
EP-1666611-A1 |
| titleOfInvention |
Diagnosis of arterial diseases by identification of a mutation in the MYH11 gene or protein |
| abstract |
The invention relates to an ex vivo method of diagnosing or predicting an arterial disease, or a risk of arterial disease, in a subject, which method comprises detecting a mutation in the MYH11 gene or protein (myosin heavy polypeptide 11 of smooth muscle cells), wherein said mutation is indicative of an arterial disease or of a risk of arterial disease. |
| isCitedBy |
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2016217965-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-108700597-A |
| priorityDate |
2004-12-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type |
http://data.epo.org/linked-data/def/patent/Publication |