http://rdf.ncbi.nlm.nih.gov/pubchem/patent/UA-20551-U
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_6869820aa9ac15d8a4f726368dbf1041 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-00 |
| filingDate | 2006-10-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f14a7a20f433d9b0a5134ebc567cac88 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_68df08102d1a7f5af9d5ce88f1733d53 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_91da8c3d480de3542e0da9bb6fe9f6df |
| publicationDate | 2007-01-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | UA-20551-U |
| titleOfInvention | Method for predicting the risk of the development of perinatal pathology in newborn infants |
| abstract | The proposed method for predicting the risk of the development of perinatal pathology in newborn infants implies determining the allele polymorphism of GSTT1 and GSTM1 genes of glutathione S-transpherases. The high inherited predisposition of the newborn infant to the disease and the enhanced risk of perinatal pathology are predicted if the deletion polymorphism of the GSTT1 gene is detected. The enhanced risk of perinatal pathology is predicted if the combination of the deletion polymorphism of the GSTT1 and GSTM1 genes is detected. |
| priorityDate | 2006-10-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 29.