About: Humans: the ultimate animal models

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

About: Humans: the ultimate animal models Goto Sponge NotDistinct Permalink

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

Attributes	Values
type	Academic Article research paper schema:ScholarlyArticle
isDefinedBy	Covid-on-the-Web dataset
has title	Humans: the ultimate animal models
Creator	Reilly, M Rossor, A
Source	Medline; PMC
abstract	covid:4a53bec35936dfbbbba23e7b0ff13458e63a2ded#abstract
has issue date	2020-08-07(xsd:dateTime)
bibo:doi	10.1136/jnnp-2020-323016
bibo:pmid	32769113
has license	no-cc
sha1sum (hex)	4a53bec35936dfbbbba23e7b0ff13458e63a2ded
schema:url	https://doi.org/10.1136/jnnp-2020-323016
resource representing a document's title	Humans: the ultimate animal models
has PubMed Central identifier	PMC7415072
has PubMed identifier	32769113
schema:publication	J Neurol Neurosurg Psychiatry
resource representing a document's body	covid:4a53bec35936dfbbbba23e7b0ff13458e63a2ded#body_text
is schema:about of	named entity 'phenotypes' named entity 'neuropathies' named entity 'rodent' named entity 'IPSC' named entity 'neurons' named entity 'alleles' named entity 'dynein' named entity 'clinical trials' named entity 'nerve fibres' named entity 'human diseases' named entity 'organoids' named entity 'CMT' named entity 'gene silencing' named entity 'motor nerve' named entity 'phenotypes' named entity 'peripheral nerves' named entity 'gap junctions' named entity 'therapeutic approaches' named entity 'neuropathies' named entity 'Charcot-Marie-Tooth disease' named entity 'DM1' named entity 'CMT' named entity 'BSCL2' named entity 'neuropathies' named entity 'genetics' named entity 'exome' named entity 'rodent models' named entity 'x-linked' named entity 'neuropathies' named entity 'human clinical trials' named entity 'inherited diseases' named entity 'pyramidal tracts' named entity 'BICD2' named entity 'pandemics' named entity 'LOF' named entity 'mutation' named entity 'disease models' named entity 'Rodents' named entity 'human trials' named entity 'neuropathies' named entity 'gene silencing' named entity 'biallelic' named entity 'molecular level' named entity 'DYNC1H1' named entity 'neuropathies' named entity 'evolution of humans' named entity 'congenital insensitivity to pain' named entity 'alleles' named entity 'pathogenesis' named entity 'genetic diseases' named entity 'Chimpanzees' named entity 'siRNA' named entity 'neurotrophins' named entity 'molecular imaging' named entity 'adolescence' named entity 'motor neuropathy' named entity 'neurological diseases' named entity 'pathogenetic' named entity 'phenotyping' named entity 'CMT' named entity 'phenotypes' named entity 'CRISPR-cas9' named entity 'adaptor protein' named entity 'text and data mining' named entity 'phenotyping' named entity 'clinical trial' named entity 'amyloidosis' named entity 'muscle' named entity 'neuropathies' named entity 'connexin 32' named entity 'myotonic dystrophy' named entity 'Charcot-Marie-Tooth disease' named entity 'TRPV4' named entity 'SPTLC1' named entity 'secretion' named entity 'autosomal recessive' named entity 'neuropathies' named entity 'FXN' named entity 'multisystem disorder' named entity 'clinical practice'

Faceted Search & Find service v1.13.91 as of Mar 24 2020

Alternative Linked Data Documents: Sponger | ODE Content Formats:

RDF

ODATA

Microdata

About

OpenLink Virtuoso version 07.20.3229 as of Jul 10 2020, on Linux (x86_64-pc-linux-gnu), Single-Server Edition (94 GB total memory)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software