http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-104450871-B
Outgoing Links
| Predicate | Object |
|---|---|
| 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/C12Q1-6883 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-32 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-11 |
| filingDate | 2013-09-25-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2019-04-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2019-04-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-104450871-B |
| titleOfInvention | Microphthalmia and anophthalmia associated gene mutation, its detection method and application thereof |
| abstract | The present invention relates to heredity ophthalmology disease fields, in particular to microphthalmia field.The present invention provides microphthalmia and anophthalmia associated gene mutation, its detection method and application thereof, the gene mutation is the ALDH1A3 gene or ALDH1A3 albumen of mutation: c.521G > A, p.Cys174Tyr. |
| priorityDate | 2013-09-25-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 138.