http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-105274235-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/C12N15-11 |
| filingDate | 2013-10-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2018-01-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2018-01-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-105274235-B |
| titleOfInvention | Application of the ABCA3 genes in congenital CCMC is detected |
| abstract | It is an object of the invention to provide a kind of ABCA3 genes to prepare the application in detecting congenital cataract microcornea syndrome (CCMC) diagnostic product, the invention provides the new purposes of ABCA3 genes, so as to provide a kind of approach for effectively carrying out congenital CCMC disease genes diagnosis, prenatal gene examination and genetic counselling, application effect shows the SNP site of gene provided by the present invention and detection primer can be effectively used for clinical patients and fetus fine hair or amniotic fluid carries out the quick detection of ABCA3 gene mutation sites. |
| priorityDate | 2013-10-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 24.