http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-106947824-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 | 2017-04-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate | 2019-09-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationDate | 2019-09-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | CN-106947824-B |
titleOfInvention | The variant sites and its detection method and purposes of obstruction sleep apnea-hypopnea syndrome tumor susceptibility gene ADIPOQ |
abstract | The present invention relates to molecular biology and medical domain, the invention discloses the variant sites of obstruction sleep apnea-hypopnea syndrome tumor susceptibility gene ADIPOQ and its detection method and the variant sites obstruction sleep apnea-hypopnea syndrome neurological susceptibility context of detection purposes, furthermore a kind of method for predicting obstruction sleep apnea-hypopnea syndrome risk by detecting the variant sites genotype is also disclosed, genomic DNA including extracting sample, specific amplification, detection, variant sites genotyping and etc., when genotypic variation occurs for the site, the risk of obstruction sleep apnea-hypopnea syndrome increases.The invention also discloses a kind of kits for detecting obstruction sleep apnea-hypopnea syndrome neurological susceptibility. |
priorityDate | 2017-04-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 157.