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http://purl.uniprot.org/citations/33346701http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/33346701http://www.w3.org/2000/01/rdf-schema#comment"Aim: To analyze the association of NKX2.5 gene with congenital heart disease (CHD), and to determine if the variants rs703752, rs3729753 and rs2277923 increase the risk for developing CHD. Materials & methods: PubMed, EBSCO and Web of Science databases were screened to identify eligible studies. Through a comprehensive meta-analysis software, the association between NKX2.5 gene variants and susceptibility of CHD was calculated by pooled odd ratio (ORs) and 95% CI. Results: We observed that the allelic model of rs703752 and rs2277923 increased the risk in the overall population: OR = 1.24; 95% CI: 1.00-1.55; Z p-value = 0.049; OR = 1.18; 95% CI: 0.01-1.37; Z p-value = 0.036; respectively. Conclusion: Our results suggested that the rs703752 and rs2277923 polymorphisms of the NKX2.5 gene are associated with CHD."xsd:string
http://purl.uniprot.org/citations/33346701http://purl.org/dc/terms/identifier"doi:10.2217/bmm-2020-0190"xsd:string
http://purl.uniprot.org/citations/33346701http://purl.uniprot.org/core/author"Vargas-Alarcon G."xsd:string
http://purl.uniprot.org/citations/33346701http://purl.uniprot.org/core/author"Rodriguez-Perez J.M."xsd:string
http://purl.uniprot.org/citations/33346701http://purl.uniprot.org/core/author"Perez-Hernandez N."xsd:string
http://purl.uniprot.org/citations/33346701http://purl.uniprot.org/core/author"Juarez-Rojop I.E."xsd:string
http://purl.uniprot.org/citations/33346701http://purl.uniprot.org/core/author"Borgonio-Cuadra V.M."xsd:string
http://purl.uniprot.org/citations/33346701http://purl.uniprot.org/core/author"Posadas-Sanchez R."xsd:string
http://purl.uniprot.org/citations/33346701http://purl.uniprot.org/core/author"Gonzalez-Castro T.B."xsd:string
http://purl.uniprot.org/citations/33346701http://purl.uniprot.org/core/author"Tovilla-Zarate C.A."xsd:string
http://purl.uniprot.org/citations/33346701http://purl.uniprot.org/core/author"Lopez-Narvaez M.L."xsd:string
http://purl.uniprot.org/citations/33346701http://purl.uniprot.org/core/author"Calderon-Colmenero J."xsd:string
http://purl.uniprot.org/citations/33346701http://purl.uniprot.org/core/author"Blachman-Braun R."xsd:string
http://purl.uniprot.org/citations/33346701http://purl.uniprot.org/core/author"Sandoval J.P."xsd:string
http://purl.uniprot.org/citations/33346701http://purl.uniprot.org/core/author"Castillo-Avila R.G."xsd:string
http://purl.uniprot.org/citations/33346701http://purl.uniprot.org/core/author"Cazarin-Santos B.G."xsd:string
http://purl.uniprot.org/citations/33346701http://purl.uniprot.org/core/author"Garcia-Flores E."xsd:string
http://purl.uniprot.org/citations/33346701http://purl.uniprot.org/core/author"Garcia-Montes J.A."xsd:string
http://purl.uniprot.org/citations/33346701http://purl.uniprot.org/core/date"2020"xsd:gYear
http://purl.uniprot.org/citations/33346701http://purl.uniprot.org/core/name"Biomark Med"xsd:string
http://purl.uniprot.org/citations/33346701http://purl.uniprot.org/core/pages"1747-1757"xsd:string
http://purl.uniprot.org/citations/33346701http://purl.uniprot.org/core/title"Association between congenital heart disease and NKX2.5 gene polymorphisms: systematic review and meta-analysis."xsd:string
http://purl.uniprot.org/citations/33346701http://purl.uniprot.org/core/volume"14"xsd:string
http://purl.uniprot.org/citations/33346701http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/33346701