http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-102257221-B1
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-156 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-158 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6883 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G16B30-00 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G16B30-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6883 |
| filingDate | 2018-07-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2021-05-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2021-05-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | KR-102257221-B1 |
| titleOfInvention | Methods for identifying new variant that cause hereditary spastic paraplegia and Diagnostic chip of hereditary spastic paraplegia |
| abstract | The present invention is a method for identifying a new variant of the cause of hereditary spastic paraplegia (HSP) disease, a system for identifying the cause of HSP disease, a computer program stored in a medium for providing information for predicting HSP, and information for HSP diagnosis. The present invention relates to a method of providing, a system for diagnosing HSP diseases, a chip for diagnosing the cause of an HSP disease, and a kit for diagnosing HSP. |
| priorityDate | 2018-07-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 467.