About: A hereditary spastic paraplegia predominant phenotype caused by variants in the NEFL gene

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About: A hereditary spastic paraplegia predominant phenotype caused by variants in the NEFL gene Goto Sponge NotDistinct Permalink

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scientific article published on 12 September 2020

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) article scientifique publié en 2020 (fr) artículu científicu espublizáu en setiembre de 2020 (ast) scientific article published on 12 September 2020 (en) наукова стаття, опублікована 12 вересня 2020 (uk) 2020 թվականի սեպտեմբերի 12-ին հրատարակված գիտական հոդված (hy)
publication date	wds:Q99731941-34FAA662-5DBC-4737-80BB-35DE3FC51EC0
publication date	2020-09-12 00:00:00Z (xsd:dateTime)
author name string	wds:Q99731941-1764249C-06DF-4EDA-932A-047D9F65884F wds:Q99731941-42F1BF5A-3C41-4A0E-8486-3CCBD0C0A645 wds:Q99731941-46F8E5C7-1930-4316-971A-C555E2BE9551 wds:Q99731941-56B388AB-69F9-48A4-81FE-39AD9A2AF052 wds:Q99731941-57B363C6-110E-4509-8EC5-F1A56AEC8CEB wds:Q99731941-5F3BE723-CF3E-4561-A822-C252DC8F150E wds:Q99731941-6FC83222-8D68-4386-885D-4C0BA5CB887A wds:Q99731941-8290A090-0AEA-43C8-8BB4-5D29F064A19D wds:Q99731941-A4903127-ABBD-477A-9017-BB63E69C49EF wds:Q99731941-B7964BB4-6234-4C9F-8E69-F51E958FFCD8
author name string	Bart P C van de Warrenburg Dennis Dooijes Erik-Jan Kamsteeg Peter Praamstra Nienke E Verbeek Karlien Mul Judith van Gaalen Meyke I Schouten Erica van der Looij Frederic A M Hennekam
rdfs:label	A hereditary spastic paraplegia predominant phenotype caused by variants in the NEFL gene (en) A hereditary spastic paraplegia predominant phenotype caused by variants in the NEFL gene (nl)
skos:prefLabel	A hereditary spastic paraplegia predominant phenotype caused by variants in the NEFL gene (en) A hereditary spastic paraplegia predominant phenotype caused by variants in the NEFL gene (nl)
name	A hereditary spastic paraplegia predominant phenotype caused by variants in the NEFL gene (en) A hereditary spastic paraplegia predominant phenotype caused by variants in the NEFL gene (nl)
author	wds:Q99731941-D4D34237-A74E-4E66-8D07-731D589A4687
author	Nicolette C Notermans
title	wds:Q99731941-D2A4BD94-6D18-43E2-B589-754E6BB2C834
title	A hereditary spastic paraplegia predominant phenotype caused by variants in the NEFL gene (en)
page(s)	wds:Q99731941-01BAD5AE-83B3-4A0F-9971-7DDC4379C08A
page(s)	98-101
instance of	wds:Q99731941-E3C9F935-18EC-4D4D-B40F-6000844C96F7
instance of	scholarly article
main subject	wds:Q99731941-19C52F5E-8572-4BAC-AE7E-6D8184C48384
main subject	hereditary spastic paraplegia
PubMed ID	wds:Q99731941-1C0CE57F-84F5-491C-993B-040E3F9DDB0C
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/32979786
PubMed ID	32979786
published in	wds:Q99731941-0DB8BE53-FF58-4FDC-B0E2-01572C3AAF14
published in	Parkinsonism and Related Disorders
volume	wds:Q99731941-1150381E-E98D-4D9F-8713-697D5998B8FD
volume	80
number of pages	wds:Q99731941-A33A34FA-C504-4E75-B01A-397083D23DD0
number of pages	4 (xsd:decimal)
DOI	wds:Q99731941-E2AED74F-5C48-434B-A312-B0EDBBDE378A
DOI	http://dx.doi.org/10.1016/J.PARKRELDIS.2020.09.016
DOI	10.1016/J.PARKRELDIS.2020.09.016
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q99731941

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