| Predicate |
Object |
| assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_e4e5159309df733f4770a2d58d46b938 |
| classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-118
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/C12Q1-6876 |
| filingDate |
2018-05-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5aa85116cf72066d1041a200bf28b520
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ffc1b40c5f4ccc26c0306bf4f78369e6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1b16a81c52a96c2402ba0439c6764571
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a563bdf4d7d6f15b746e423b15ce494c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e12a4f3021d8af00d6e8b22013f77c62 |
| publicationDate |
2019-01-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber |
TW-201900885-A |
| titleOfInvention |
Method for detecting high risk of bronchopulmonary hypoplasia and introduction group for genotyping of NQO1 gene and method thereof |
| abstract |
The present invention discloses a method for detecting the high risk of bronchopulmonary dysplasia (BPD) in preterm infants. The method includes genotyping the rs1800566 SNP of the NQO1 gene in a genomic DNA sample, wherein the genomic DNA sample is from the premature baby or the mother of the premature baby, and if the genotype of the rs1800566 SNP is TT, the judgment This premature infant is at risk of developing BPD. The invention also discloses a primer set and a method for genotyping the rs1800566 SNP of the NQO1 gene. |
| priorityDate |
2017-05-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type |
http://data.epo.org/linked-data/def/patent/Publication |