About: CASZ1 loss-of-function mutation associated with congenital heart disease

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scientific journal article

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rdf:type	Item
description	article scientifique publié en 2016 (fr) artículu científicu espublizáu en 2016 (ast) vědecký článek publikovaný v roce 2016 (cs) 2016 թվականի դեկտեմբերին հրատարակված գիտական հոդված (hy) 2016 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած (hyw) наукова стаття, опублікована в грудні 2016 (uk) vedecký článok (publikovaný 2016/12/20) (sk) مقالة علمية (نشرت في 20-12-2016) (ar) wetenschappelijk artikel (gepubliceerd op 2016/12/20) (nl) scientific journal article (en) im Dezember 2016 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q28114856-E6A89DC0-A7BA-4990-952D-C43C3DEBA632
publication date	2016-12-20 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q28114856-96728403-75B6-4797-8277-96D1990F2CE9
language of work or name	English
author name string	wds:Q28114856-023AF484-E5F1-4580-9FBB-682AC94EF6FA wds:Q28114856-12E9C331-4930-4F9F-89D7-D39ED0CD9AB4 wds:Q28114856-2480547D-A714-434C-9437-35BFCE12EEA6 wds:Q28114856-2DDC3E03-98DA-4196-B463-39443C4F2556 wds:Q28114856-5AF91DEB-1FB1-490E-8F7B-70071B1582DF wds:Q28114856-5DB7E18E-6960-4907-A168-F5DBF4F9F468 wds:Q28114856-66210B3A-FC08-40BA-A5C1-3E84BB49DBC7 wds:Q28114856-67C35C13-0349-4A17-8358-71379265551C wds:Q28114856-6C9C3785-077F-4E70-A3A1-5A637B07FB48 wds:Q28114856-7716790A-7517-46FE-85AD-7340F0FE4303 wds:Q28114856-9876F635-9A41-44C8-AE88-33DECDA7B29C wds:Q28114856-9B233B17-F053-4839-95AB-6B2D620BDA1D wds:Q28114856-C79BAF52-6259-4229-B1E2-C8551DB9D7C6 wds:Q28114856-C86E2091-B40A-498F-8A5D-4979DE3B04B3 wds:Q28114856-D26D524F-FCC3-4F21-B979-CB4144FF34AC
author name string	Hua Liu Ning Li Yan-Jie Li Juan Wang Song Xue Ri-Tai Huang Yi-Qing Yang Xiao-Dong Zhang Xiao-Xiao Yang Xing-Biao Qiu Ruo-Gu Li Xin-Kai Qu Jia-Hong Xu Jian-Yun Gu Ying-Jia Xu
rdfs:label	CASZ1 loss-of-function mutation associated with congenital heart disease (en) CASZ1 loss-of-function mutation associated with congenital heart disease (nl) CASZ1 loss-of-function mutation associated with congenital heart disease (ast)
skos:prefLabel	CASZ1 loss-of-function mutation associated with congenital heart disease (en) CASZ1 loss-of-function mutation associated with congenital heart disease (nl) CASZ1 loss-of-function mutation associated with congenital heart disease (ast)
name	CASZ1 loss-of-function mutation associated with congenital heart disease (en) CASZ1 loss-of-function mutation associated with congenital heart disease (nl) CASZ1 loss-of-function mutation associated with congenital heart disease (ast)
title	wds:Q28114856-FA87C811-61A0-4330-8837-C638EDEE5ACC
title	CASZ1 loss-of-function mutation associated with congenital heart disease (en)
page(s)	wds:Q28114856-9852D111-95A0-476D-88EB-C695F20D9589
page(s)	62–68
instance of	wds:Q28114856-B01A4933-F37E-4E92-9F03-AD6B0EC1347F
instance of	scholarly article
main subject	wds:Q28114856-70C8B27E-DD91-4B90-B27E-CEDF12E688F6 wds:Q28114856-AB52D79B-2C69-4BBC-A45C-CA0EA21F6FD1 wds:Q28114856-DC5852D7-9FFD-4B62-A1D8-C3EBAABB445A
main subject	congenital heart disease positive regulation of transcription, DNA-templated Castor zinc finger 1
PubMed ID	wds:Q28114856-77443324-2AC6-43FA-8DA0-190A6749B834
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/27693370
PubMed ID	27693370
published in	wds:Q28114856-D230E8E5-1896-49DB-89F9-3F6384FAF303
published in	Gene
issue	wds:Q28114856-037C56A0-5FE0-49D1-987E-76C0A17F5AD2
volume	wds:Q28114856-53885696-EAA9-4A25-A881-71861B6109E2
issue	1
volume	595
DOI	wds:Q28114856-735DCFBD-148E-4DCB-9F2E-8E94964CABFC
DOI	http://dx.doi.org/10.1016/J.GENE.2016.09.044
DOI	10.1016/J.GENE.2016.09.044
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q28114856
is cites work of	A novel de novo CASZ1 heterozygous frameshift variant causes dilated cardiomyopathy and left ventricular noncompaction cardiomyopathy The Prognostic Significance of Protein Expression of CASZ1 in Clear Cell Renal Cell Carcinoma Genome-Wide Association Study of Apparent Treatment-Resistant Hypertension in the CHARGE Consortium: The CHARGE Pharmacogenetics Working Group MEF2C loss-of-function mutation contributes to congenital heart defects A Novel MEF2C Loss-of-Function Mutation Associated with Congenital Double Outlet Right Ventricle. Application of Whole Genome Sequencing Technology in the Investigation of Genetic Causes of Fetal, Perinatal, and Early Infant Death Genetics of Congenital Heart Disease CASZ1b is a novel transcriptional corepressor of mineralocorticoid receptor HAND1 Loss-of-Function Mutation Causes Tetralogy of Fallot. CASZ1 induces skeletal muscle and rhabdomyosarcoma differentiation through a feed-forward loop with MYOD and MYOG
is cites work of	wds:Q91575536-3FEE86CD-E292-490C-927D-03FFC03A8B15 wds:Q93088413-E1F9F2D0-A8D1-444C-8C51-A4DD31ECCC46 wds:Q90215760-6665B407-B63E-4F40-AA20-558B3838DD1C wds:Q46186008-F065A974-E2F5-4ABB-8043-0F0C990C047E wds:Q100737200-2CE988A9-DD1E-4D73-94EE-40A549E85900 wds:Q43466893-8246229C-12B0-45A2-A5F2-B4DEBB2C8555 wds:Q89722579-D1935243-FAA3-4BFA-B150-7543492A9233 wds:Q51273200-B4B42E6D-64DC-4A83-8615-64554CC00AC4 wds:Q52691186-60AF337D-BA47-42DE-A74F-50C1BE98EF6C wds:Q92327415-B584AE9E-D2B3-499C-89AB-67D97336AA43

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