http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2741861-C1
Outgoing Links
Predicate | Object |
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_5205c25b782ff85e96fda9512faca381 |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-582 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6876 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-50 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68 |
filingDate | 2020-08-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate | 2021-01-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_caefdafc3544f477a99c5c632ac499cb http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7dffe6764064709e153944cceb87dbcf http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ca253b75f42271f6cb810f44aa9db5b2 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_85a3851c6f3aa27d476cedb6f2a15617 |
publicationDate | 2021-01-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | RU-2741861-C1 |
titleOfInvention | Method for predicting newborn weight in pregnant women with preeclampsia in combination with fetal growth retardation syndrome |
abstract | FIELD: medical diagnostics.SUBSTANCE: method is proposed for predicting the weight of a newborn in pregnant women of Russian ethnicity who are natives of the Central Black Earth Region of Russia with preeclampsia, who do not have a family history of preeclampsia, and in combination with fetal growth retardation syndrome. DNA is isolated from peripheral venous blood, analysis of rs5985 polymorphism of F13A1 gene, prediction of the normal weight of a newborn when detecting the T allele of the polymorphic locus rs5985 of F13A1 gene, predicting low weight of a newborn when detecting G allele of F13A1 gene polymorphism.EFFECT: invention provides for obtaining criteria for assessing prognosis of the weight of a newborn in pregnant women with preeclampsia in combination with fetal growth retardation syndrome based on data on rs5985 polymorphism of F13A1 gene.1 cl, 1 dwg, 1 tbl, 4 ex |
isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2786313-C1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2775436-C1 |
priorityDate | 2020-08-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 52.