| http://purl.uniprot.org/citations/31738640 | http://www.w3.org/1999/02/22-rdf-syntax-ns#type | http://purl.uniprot.org/core/Journal_Citation |
| http://purl.uniprot.org/citations/31738640 | http://www.w3.org/2000/01/rdf-schema#comment | "BackgroundHirschsprung's disease (HSCR) is a heterogeneous congenital malformation of the enteric nervous system with a complex genetic etiology. We investigated if there was an association between Neuregulin-1 (NRG1) rs7835688 G > C, rs16879552 T > C and rs2439302 G > C polymorphisms and the risk of HSCR. Methods: We determined and compared the frequency of NRG1 polymorphisms rs7835688 G > C, rs16879552 T > C and rs2439302 G > C in 70 children with HSCR and 90 controls by TaqMan SNPs genotyping assays. Results: No significant differences in allele or genotype frequencies of NRG1 rs7835688 G > C, rs16879552 T > C and rs2439302 G > C polymorphisms were observed between HSCR cases and controls. Analyses showed that the NRG1 rs7835688 G > C, rs16879552 T > C and rs2439302 G > C polymorphisms were not significantly associated with an increased risk of non-syndromic HSCR. Conclusions: Our findings suggested that NRG1 rs7835688 G > C, rs16879552 T > C and rs2439302 G > C polymorphisms are not a risk factor in development of HSCR."xsd:string |
| http://purl.uniprot.org/citations/31738640 | http://purl.org/dc/terms/identifier | "doi:10.1080/15513815.2019.1692113"xsd:string |
| http://purl.uniprot.org/citations/31738640 | http://purl.uniprot.org/core/author | "Salehi E."xsd:string |
| http://purl.uniprot.org/citations/31738640 | http://purl.uniprot.org/core/author | "Neamatzadeh H."xsd:string |
| http://purl.uniprot.org/citations/31738640 | http://purl.uniprot.org/core/author | "Aflatoonian M."xsd:string |
| http://purl.uniprot.org/citations/31738640 | http://purl.uniprot.org/core/author | "Dastgheib S.A."xsd:string |
| http://purl.uniprot.org/citations/31738640 | http://purl.uniprot.org/core/author | "Amooee A."xsd:string |
| http://purl.uniprot.org/citations/31738640 | http://purl.uniprot.org/core/author | "Bahrami R."xsd:string |
| http://purl.uniprot.org/citations/31738640 | http://purl.uniprot.org/core/author | "Hosseini-Jangjou S.H."xsd:string |
| http://purl.uniprot.org/citations/31738640 | http://purl.uniprot.org/core/author | "Sadeghizadeh-Yazdi J."xsd:string |
| http://purl.uniprot.org/citations/31738640 | http://purl.uniprot.org/core/date | "2021"xsd:gYear |
| http://purl.uniprot.org/citations/31738640 | http://purl.uniprot.org/core/name | "Fetal Pediatr Pathol"xsd:string |
| http://purl.uniprot.org/citations/31738640 | http://purl.uniprot.org/core/pages | "198-205"xsd:string |
| http://purl.uniprot.org/citations/31738640 | http://purl.uniprot.org/core/title | "Association of Neuregulin 1 rs7835688 G > C, rs16879552 T > C and rs2439302 G > C Polymorphisms with Susceptibility to Non-Syndromic Hirschsprung's Disease."xsd:string |
| http://purl.uniprot.org/citations/31738640 | http://purl.uniprot.org/core/volume | "40"xsd:string |
| http://purl.uniprot.org/citations/31738640 | http://www.w3.org/2004/02/skos/core#exactMatch | http://purl.uniprot.org/pubmed/31738640 |
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| http://purl.uniprot.org/uniprot/#_A6MW55-mappedCitation-31738640 | http://www.w3.org/1999/02/22-rdf-syntax-ns#object | http://purl.uniprot.org/citations/31738640 |
| http://purl.uniprot.org/uniprot/#_A6MW56-mappedCitation-31738640 | http://www.w3.org/1999/02/22-rdf-syntax-ns#object | http://purl.uniprot.org/citations/31738640 |
| http://purl.uniprot.org/uniprot/#_A0A494C1B5-mappedCitation-31738640 | http://www.w3.org/1999/02/22-rdf-syntax-ns#object | http://purl.uniprot.org/citations/31738640 |
| http://purl.uniprot.org/uniprot/#_A0A494C1F5-mappedCitation-31738640 | http://www.w3.org/1999/02/22-rdf-syntax-ns#object | http://purl.uniprot.org/citations/31738640 |
| http://purl.uniprot.org/uniprot/#_A0A494C1F8-mappedCitation-31738640 | http://www.w3.org/1999/02/22-rdf-syntax-ns#object | http://purl.uniprot.org/citations/31738640 |