About: Cloning of the human genomic amiloride-sensitive Na+/H+ antiporter gene, identification of genetic polymorphisms, and localization on the genetic map of chromosome 1p

Facets (new session)
Description
Metadata
Settings
- owl:sameAs
- Inference Rule:

About: Cloning of the human genomic amiloride-sensitive Na+/H+ antiporter gene, identification of genetic polymorphisms, and localization on the genetic map of chromosome 1p Goto Sponge NotDistinct Permalink

An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

scientific article published on 01 May 1990

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в травні 1990 (uk) im Mai 1990 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en mayu de 1990 (ast) scientific article published on 01 May 1990 (en)
publication date	wds:Q68087203-80386FF4-6BC9-4F5A-AF36-9D414D7E13C3
publication date	1990-05-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q68087203-646D3E28-2058-4E73-B800-AE0F6C646349 wds:Q68087203-CE195B9F-9C1A-4B84-8169-64F15F713D21
author name string	R P Lifton C Sardet
rdfs:label	Cloning of the human genomic amiloride-sensitive Na+/H+ antiporter gene, identification of genetic polymorphisms, and localization on the genetic map of chromosome 1p (en) Cloning of the human genomic amiloride-sensitive Na+/H+ antiporter gene, identification of genetic polymorphisms, and localization on the genetic map of chromosome 1p (nl)
skos:prefLabel	Cloning of the human genomic amiloride-sensitive Na+/H+ antiporter gene, identification of genetic polymorphisms, and localization on the genetic map of chromosome 1p (en) Cloning of the human genomic amiloride-sensitive Na+/H+ antiporter gene, identification of genetic polymorphisms, and localization on the genetic map of chromosome 1p (nl)
name	Cloning of the human genomic amiloride-sensitive Na+/H+ antiporter gene, identification of genetic polymorphisms, and localization on the genetic map of chromosome 1p (en) Cloning of the human genomic amiloride-sensitive Na+/H+ antiporter gene, identification of genetic polymorphisms, and localization on the genetic map of chromosome 1p (nl)
author	wds:Q68087203-5184BDAD-0411-428C-922A-9CD0A6E29B00 wds:Q68087203-C2049641-C77D-49A4-AD24-5F5731A3E33D
author	Jacques Pouysségur Jean-Marc Lalouel
title	wds:Q68087203-6661BF4B-D51A-4946-A99E-FCDA9FD4B2A5
title	Cloning of the human genomic amiloride-sensitive Na+/H+ antiporter gene, identification of genetic polymorphisms, and localization on the genetic map of chromosome 1p (en)
page(s)	wds:Q68087203-803F4E7E-1B0E-4F65-A158-3559EDB467CD
page(s)	131-135
instance of	wds:Q68087203-504138B4-A1F3-41A9-8E5E-4207B6E3885E
instance of	scholarly article
PubMed ID	wds:Q68087203-87A4C96E-B434-424D-AC75-448234B1F1B5
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/1970796
PubMed ID	1970796
published in	wds:Q68087203-43582FAB-06EA-4E62-B9AB-E44E270122CE
published in	Genomics
issue	wds:Q68087203-A12AE699-CB65-48CC-BB7F-CE86A2C5D582
volume	wds:Q68087203-7AD593EF-8EC7-4848-97FC-538669F90A9F
issue	1
volume	7
DOI	wds:Q68087203-3FF154A2-6084-4EF9-8E4A-D9861D287F5A
DOI	http://dx.doi.org/10.1016/0888-7543(90)90530-8
DOI	10.1016/0888-7543(90)90530-8
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q68087203
is cites work of	Comparative map for mice and humans A chimaeric llβ-hydroxylase/aldosterone synthase gene causes glucocorticoid-remediable aldosteronism and human hypertension Constitutional 1p36 deletion in a child with neuroblastoma. Use of the single-strand conformation polymorphism technique to detect loss of heterozygosity in neuroblastoma Hereditary hypertension caused by chimaeric gene duplications and ectopic expression of aldosterone synthase Evidence for effective suppression of recombination in the chromosome 17q21 segment spanning RNU2-BRCA1. Silent Polymorphisms within the Coding Region of Human Sodium/Hydrogen Exchanger Isoform-1 cDNA in Peripheral Blood Mononuclear Cells of Leukemia Patients Comparative map for mice and humans Genetic susceptibility to nephropathy in insulin-dependent diabetes: from epidemiology to molecular genetics. An exclusion map for pre-eclampsia: assuming autosomal recessive inheritance Chromosomal localization of the human renal sodium phosphate transporter to chromosome 5: implications for X-linked hypophosphatemia. Abnormalities in insulin sensitivity, vascular resistance and erythrocyte cation transport are independent genetic traits in familial hypertension
is cites work of	wds:Q67871559-1EADD89C-627C-4000-8730-44AE9BC65168 wds:Q72087885-A9637876-BFEB-4D3C-8E2E-877A9482002E wds:Q28208090-77C0CA6B-B3E1-4B92-99EE-A4C46B200E3A wds:Q35194318-7EAA459A-6369-43AE-93EB-F5D3DC6707DD wds:Q35195615-79C8DDA6-6A7F-46BB-B1FA-B07FA91A8830 wds:Q42476312-09444343-B8F3-4D3C-A21B-EF5C16946426 wds:Q49109372-8F1A2109-FFF1-4DF8-A838-04F6DDFBCE5B wds:Q35364327-99DC8073-1E9D-4C19-8E22-E88B1CB519B1 wds:Q55671192-90BA21E0-BD7F-432F-98D4-5DB5426FE4BA wds:Q34389623-6F93D780-9F50-4A5A-8188-D788EA929EDF wds:Q41041149-7A2AF380-9A7D-4255-875B-ADD3F1FB37A5 wds:Q56551580-FF1DD26B-883C-42D8-9206-CFE9D5637420

Faceted Search & Find service v1.16.117 as of May 05 2024

Alternative Linked Data Documents: ODE Content Formats:

RDF

ODATA

Microdata

About

OpenLink Virtuoso version 07.20.3239 as of May 5 2024, on Linux (x86_64-centos_6-linux-gnu), Single-Server Edition (378 GB total memory, 180 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2025 OpenLink Software