About: Human immune disorder associated with homozygous hypomorphic mutation affecting MALT1B splice variant

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About: Human immune disorder associated with homozygous hypomorphic mutation affecting MALT1B splice variant Goto Sponge NotDistinct Permalink

An Entity of Type : schema:ScholarlyArticle, within Data Space : wasabi.inria.fr associated with source document(s)

Attributes	Values
type	Academic Article research paper schema:ScholarlyArticle
isDefinedBy	Covid-on-the-Web dataset
title	Human immune disorder associated with homozygous hypomorphic mutation affecting MALT1B splice variant
Creator	Aksu, Guzide Aykut, Ayca Cogulu, Ozgur Durmaz, Asude Gehring, Torben Gewies, Andreas Graß, Carina Karaca, Neslihan Krappmann, Daniel Kutukculer, Necil O'neill, Thomas Seeholzer, Thomas
source	PMC
abstract	covid:5c2e8410de91adcb038f6003531705f47dd61c32#abstract
has issue date	2020-08-25(xsd:dateTime)
bibo:doi	10.1016/j.jaci.2020.07.034
has license	no-cc
sha1sum (hex)	5c2e8410de91adcb038f6003531705f47dd61c32
schema:url	https://doi.org/10.1016/j.jaci.2020.07.034
resource representing a document's title	Human immune disorder associated with homozygous hypomorphic mutation affecting MALT1B splice variant
has PubMed Central identifier	PMC7445549
schema:publication	J Allergy Clin Immunol
resource representing a document's body	covid:5c2e8410de91adcb038f6003531705f47dd61c32#body_text
is schema:about of	named entity 'immune disorder' named entity 'homozygous' named entity 'splice variant' named entity 'homozygous' named entity 'hypomorphic' named entity 'mutation' named entity 'CD28' named entity 'transversion' named entity 'NF-κB' named entity 'Ion' named entity 'TRAF6' named entity 'cytokine' named entity 'next-generation sequencing' named entity 'squamous epithelium' named entity 'MALT1' named entity 'germline' named entity 'C-terminal' named entity 'bronchopneumonia' named entity 'clinical features' named entity 'TRAF6' named entity 'lymphadenopathies' named entity 'MALT1' named entity 'hypomorphic' named entity 'lung' named entity 'ligation' named entity 'malignancy' named entity 'transduced' named entity 'pathology' named entity 'atelectasis' named entity 'protease' named entity 'co-stimulation' named entity 'Ion' named entity 'MALT1' named entity 'CD28' named entity 'isoform' named entity 'protease' named entity 'MALT1' named entity 'CARMA1' named entity 'Human blood' named entity 'hyperplasia' named entity 'CD8+ T cell' named entity 'hypomorphic' named entity 'bronchiectasis' named entity 'kidney' named entity 'primary immunodeficiencies' named entity 'hypomorphic' named entity 'abdominal ultrasonography' named entity 'MALT1' named entity 'CD4+ T cells' named entity 'scalp' named entity 'splenomegaly' named entity 'CD28' named entity 'psoriasis' named entity 'immune deficiency' named entity 'loss-of-function mutation' named entity 'TNFα' named entity 'flow cytometry' named entity 'gene' named entity 'MALT1' named entity 'genetic mutations' named entity 'NF-κB' named entity 'MALT1' named entity 'autoimmunity' named entity 'cutaneous' named entity 'adaptive immune response' named entity 'purulent' named entity 'MALT1' named entity 'NF-κB' named entity 'MALT1' named entity 'NF-κB' named entity 'immune disorder' named entity 'gene'

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