http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2012139170-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_13f6fdfd25f26be8eaf14fdfe49048e2 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-09 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68 |
| filingDate | 2010-12-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c000e8bc4513271493718eb9f01d0b64 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_73f6a5cd95e5d1ae949882897297f67b |
| publicationDate | 2012-07-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-2012139170-A |
| titleOfInvention | Primer, probe, microarray for detecting mutation of EYS gene, detection kit provided with the same, method for examining gene mutation causing retinitis pigmentosa, method for examining genetic susceptibility to retinitis pigmentosa |
| abstract | A novel gene mutation of retinal pigment degeneration causative gene EYS c. Provided are a primer, a probe, a microarray, a detection kit including these, a detection method for detecting RP-causing gene mutation, and a method for testing genetic susceptibility to RP for detecting the 4957_4958InsA mutation. In the EYS gene, c. In a DNA-containing sample taken from a patient with retinitis pigmentosa by using primers, probes, and microarrays that can detect the 4957_4958InsA mutation, c. The presence or absence of the 4957_4958InsA mutation is examined. [Selection] Figure 3 |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-102025041-B1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2023163131-A1 |
| priorityDate | 2010-12-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 61.