http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-104789572-B
Outgoing Links
| Predicate | Object |
|---|---|
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-63 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-12 |
| filingDate | 2015-05-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2017-12-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2017-12-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-104789572-B |
| titleOfInvention | GPRASP2 mutated genes, its authentication method and detection kit |
| abstract | The invention discloses GPRASP2 Mutated genes, its authentication method and detection kit, GPRASP2 Mutated genes, it is people's GPRASP2 The 1717th ~ 1718 nucleotides GC mutation of the 5th exons coding region sequence of gene order turns into nucleotides AA, and the present invention utilizes the Disease-causing gene of the human genome exon trapping scientific discovery genetic disease.This method is convenient, convenient, and due to need to only take the gene mutation sample of one or a small amount of to carry out human genome exon sequence capture, greatly reduces cost.The identification of the gene is to syndromic deafness（Syndromic Hearing Loss, SHL）Gene diagnosis susceptible and that crowd occurs has important value, to exploring SHL pathogenesis and to open up new therapy approach significant. |
| priorityDate | 2015-05-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
| Predicate | Subject |
|---|---|
| isDiscussedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID114928 http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5543 http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID414858648 |
Total number of triples: 14.