Not logged in :
Login
(Sponging disallowed)
Facets (new session)
Description
Metadata
Settings
Rule:
ActivityStreamsMap
asEquivalent
b3s
b3sifp
cciso
facets
http://demo.openlinksw.com/dataspace
http://www.w3.org/2002/07/owl#
ldp
oplweb
rel-me-auth
skos-trans
sql-vdb-data-lake
urn:ALKAdatareduced
urn:analytics:acqof:rule
urn:clothing:rule:qa
urn:det:rdf:label
urn:inference:oplfaq:rule
urn:inference:product:feature:inverse:rule
urn:ingleng:inf:demo:inf:rule
urn:kbpedia:actor:subclass:test:rules
urn:kbpedia:comedian:owl:equivalent:class:subproperty:inference:rules
urn:kbpedia:mime-artist:owl:equivalent:class:subproperty:inference:rules
urn:kbpedia:owl:equivalent:class:subproperty:inference:rules
urn:kbpedia:philosopher:owl:equivalent:class:subproperty:inference:rules
urn:kbpedia:stage-actor:owl:equivalent:class:subproperty:inference:rules
urn:kgdemo:1:ifp:rule
urn:kgdemo:1:ifp:rule2
urn:lava:demo:rule
urn:owl:equivalent:class:inference:rules
urn:rdfs:subclass:subproperty:inference:rules
urn:rdfs:type:wikidata:rule
urn:recon:data:ifp
urn:recon:data:ifp:rule
urn:recruitment:rule:built-in:rule
urn:rsm12e:translation:rule
urn:rxnorm:data:rule
urn:se:demo:inference:rule
urn:test:skos:inverse:rule
urn:wireless:plans:features:builtin:inference:rule:1
virtrdf-eturtle-containers
virtrdf-hashtag
virtrdf-ifp
virtrdf-label
virtrdf-meta-entity-class
virtrdf-url
None
Inverse Functional Properties:
Disabled (fastest)
Apply to subjects only
Apply to objects only
Apply to both subjects and objects
"Same As":
Disabled (fastest)
Apply to subjects only
Apply to objects only
Apply to both subjects and objects (recommended)
Apply to subjects, objects and predicates (not recommended on big datasets)
Apply to predicates only (special use cases only)
About:
Noonan syndrome 9
Goto
Sponge
NotDistinct
Permalink
An Entity of Type :
owl:Class
, within Data Space :
linkeddata.uriburner.com:28898
associated with source
document(s)
New Facet based on Instances of this Class
Attributes
Values
type
Class
subClassOf
autosomal dominant disease
Noonan syndrome
nodeID://b50939100
label
Noonan syndrome 9
described by
https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id
DOID:0060587
has_alternative_id
DOID:0070109
database_cross_reference
ICD10CM:Q87.1
OMIM:616559
has_exact_synonym
NS9
(en)
has_obo_namespace
disease_ontology
http://purl.obolib...g/obo/IAO_0000115
A Noonan syndrome that has_material_basis_in heterozygous mutation in the SOS2 gene on chromosome 14q21.
is
topic
of
Human Disease Ontology
is
annotatedSource
of
nodeID://b50939101
Faceted Search & Find service v1.17_git144 as of Jul 26 2024
Alternative Linked Data Documents:
iSPARQL
|
ODE
Content Formats:
RDF
ODATA
Microdata
About
OpenLink Virtuoso
version 08.03.3331 as of Aug 25 2024, on Linux (x86_64-ubuntu_noble-linux-glibc2.38-64), Single-Server Edition (378 GB total memory, 15 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software