About: Pitfalls of ABO Genotyping Based on Targeted Single Nucleotide Variant Analysis Due to a Nondeletional O Allele Lacking c.261delG: First Report of ABO*O.09.01 in Korea

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scientific article published on 01 November 2019

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) scientific article published on 01 November 2019 (en) artículu científicu espublizáu en payares de 2019 (ast) наукова стаття, опублікована 1 листопада 2019 (uk)
publication date	wds:Q93035887-DEE6E7F5-031B-41A5-A25E-0F536B88246B
publication date	2019-11-01 00:00:00Z (xsd:dateTime)
cites work	wds:Q93035887-21D47837-6413-4AE2-96FB-735DF9054CDC wds:Q93035887-8B105DE9-3F22-4A3E-B862-1AA14CD93ACD wds:Q93035887-9906579E-482E-40E0-B02A-02474BE55D73 wds:Q93035887-B29F9E09-2BAD-4E79-825C-9BFF9E92EDF5 wds:Q93035887-B704AD5D-06EE-46CF-B972-2ABA4514C2CF wds:Q93035887-D9802A99-DCBA-48DD-BAE2-3BD31FFAE184 wds:Q93035887-DD0342EF-6C35-46C1-97DF-643F89BE1A4D wds:Q93035887-E42E14FB-88F5-48B5-8D5E-B599E0B06E28 wds:Q93035887-F1888BC9-A11E-4A3C-A7C0-A0103335BA7D
cites work	Molecular genetic basis of the histo-blood group ABO system. Sequence variation at the human ABO locus. Recombination and gene conversion-like events may contribute to ABO gene diversity causing various phenotypes Nondeletional ABOO alleles frequently cause blood donor typing problems. Blood grouping discrepancies between ABO genotype and phenotype caused by O alleles. New and unusual O alleles at the ABO locus are implicated in unexpected blood group phenotypes. [Analysis for Eight ABO Alleles in Korean Population.]. Nondeletional ABOO alleles express weak blood group A phenotypes A clue to the basis of allelic enhancement: occurrence of the Ax subgroup in the offspring of blood group O parents
rdfs:label	Pitfalls of ABO Genotyping Based on Targeted Single Nucleotide Variant Analysis Due to a Nondeletional O Allele Lacking c.261delG: First Report of ABOO.09.01 in Korea (en) Pitfalls of ABO Genotyping Based on Targeted Single Nucleotide Variant Analysis Due to a Nondeletional O Allele Lacking c.261delG: First Report of ABOO.09.01 in Korea (nl)
skos:prefLabel	Pitfalls of ABO Genotyping Based on Targeted Single Nucleotide Variant Analysis Due to a Nondeletional O Allele Lacking c.261delG: First Report of ABOO.09.01 in Korea (en) Pitfalls of ABO Genotyping Based on Targeted Single Nucleotide Variant Analysis Due to a Nondeletional O Allele Lacking c.261delG: First Report of ABOO.09.01 in Korea (nl)
name	Pitfalls of ABO Genotyping Based on Targeted Single Nucleotide Variant Analysis Due to a Nondeletional O Allele Lacking c.261delG: First Report of ABOO.09.01 in Korea (en) Pitfalls of ABO Genotyping Based on Targeted Single Nucleotide Variant Analysis Due to a Nondeletional O Allele Lacking c.261delG: First Report of ABOO.09.01 in Korea (nl)
author	wds:Q93035887-104106EC-DE1E-4D7A-8DCD-AEE9D84EE2F6 wds:Q93035887-1A52014E-49A5-45DA-9AA7-883C96A0A7C4 wds:Q93035887-271B54C2-A769-4C08-BA92-5BA937418110 wds:Q93035887-452590FF-22C3-4B64-B302-B4D69D960981 wds:Q93035887-63069247-99A8-4D1B-888C-9F62178E3E88 wds:Q93035887-C1984909-AF13-47EE-8C57-58418BE989EE wds:Q93035887-CDE46F43-1293-4016-855E-729789D32FB2 wds:Q93035887-D75287EC-9DDA-4600-894A-278D69F021D1 wds:Q93035887-FE90CE1A-FA4D-4479-AB6F-CDB20F5A4F64
author	Moon-Woo Seong Sung Wook Park Sung Im Cho Man Jin Kim Hyungsuk Kim Da Young Song Tae Yeul Kim Dahae Yang Boram Kim
title	wds:Q93035887-3867EBA9-B410-4C9F-A840-03282913AA67
title	Pitfalls of ABO Genotyping Based on Targeted Single Nucleotide Variant Analysis Due to a Nondeletional O Allele Lacking c.261delG: First Report of ABO*O.09.01 in Korea (en)
page(s)	wds:Q93035887-AB7398DD-DB1B-47A8-BE35-DC1ADD4BA133
page(s)	599-601
instance of	wds:Q93035887-27EF0201-D5E7-4EE9-9CEF-6A4F71B973D1 wds:Q93035887-6518cff3-83d8-4453-8a35-37de8abcef16
instance of	scholarly article case report
PubMed ID	wds:Q93035887-779C0506-AC5D-41D0-915E-0AE231644FCA
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/31240894
PubMed ID	31240894
published in	wds:Q93035887-2236742C-4F2E-4EB1-A8F8-6933C0FA7DDA
published in	Annals of laboratory medicine
issue	wds:Q93035887-6FE3C146-C52C-44EF-A96C-2A11CBAD10D8
volume	wds:Q93035887-0D99AD97-9EB3-4AEF-860E-D919504F9665
issue	6
volume	39
DOI	wds:Q93035887-B37FF8A2-5953-49E1-BB47-5E7947567A38
DOI	http://dx.doi.org/10.3343/ALM.2019.39.6.599
DOI	10.3343/ALM.2019.39.6.599
copyright license	wds:Q93035887-258bf75b-1172-49d3-888b-3546d55addb3
copyright status	wds:Q93035887-ac40d4d8-e09b-4659-b4ca-f4d217696bd7
copyright license	Creative Commons Attribution-NonCommercial 4.0 International
copyright status	copyrighted
PMCID	wds:Q93035887-B165D4E8-D96F-467D-9A1F-B8E9F0EA5C10
PMCID	6660326
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q93035887

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