http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2625003-C1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_aee5bcd773958f7940475c4d950eaf54 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6806 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N1-00 |
| filingDate | 2016-10-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2017-07-11-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_721541fc2ada83eab2aabfc8594c9237 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_23b26b4594e6a2de586c8b838e2e68c2 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f88f74c6b0862775da7a0ea156c262d2 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_34c2b129b62a7fcbfe420a86ad92f55e |
| publicationDate | 2017-07-11-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | RU-2625003-C1 |
| titleOfInvention | Nucleotid sequence set for medical technology of detection of dmd gene deleteions most particular in russia by multiplex pcr/aflp analysis |
| abstract | FIELD: biotechnology. n SUBSTANCE: set of nucleotide sequences that can be used to diagnose frequent deletions of the DMD gene responsible for Duchenne/Becker muscular dystrophy in the RF population, based on mutation frequencies among patients resident in the Russian Federation. Diagnosis of deletions affects the promoter region; 3, 4, 6, 8, 13, 17, 19, 32 42, 43, 44, 45, 47, 48, 50, 51, 52, 53, 60 exons of the DMD gene in the hemizygotic state. n EFFECT: improved efficiency of deletions diagnosing. n 1 dwg |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2772504-C1 |
| priorityDate | 2016-10-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 79.