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http://demo.openlinksw.com/dataspace
http://www.w3.org/2002/07/owl#
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urn:kbpedia:mime-artist:owl:equivalent:class:subproperty:inference:rules
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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
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urn:recon:data:ifp:rule
urn:recruitment:rule:built-in:rule
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urn:se:demo:inference:rule
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About: nodeID://b50940505
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An Entity of Type :
owl:Axiom
, within Data Space :
linkeddata.uriburner.com:28898
associated with source
document(s)
Type:
Axiom
New Facet based on Instances of this Class
Attributes
Values
type
Axiom
described by
https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
Type
http://purl.obolibrary.org/obo/ECO_0007637
http://purl.obolibrary.org/obo/ECO_0007638
http://purl.obolibrary.org/obo/ECO_0007645
http://purl.obolibrary.org/obo/ECO_0007646
annotatedProperty
http://purl.obolibrary.org/obo/IAO_0000115
annotatedSource
X-linked adrenal hypoplasia congenita
annotatedTarget
An adrenal cortical hypofunction that is characterized by a reduction in adrenal gland function resulting from incomplete development of the adrenal cortex and has_material_basis_in the nuclear receptor NR0B1 (DAX1) gene.
database_cross_reference
url:http://press.endocrine.org/doi/full/10.1210/jcem.83.8.5027
url:https://ghr.nlm.nih.gov/condition/x-linked-adrenal-hypoplasia-congenita#genes
url:https://en.wikipedia.org/wiki/X-linked_adrenal_hypoplasia_congenita
url:http://www.ncbi.nlm.nih.gov/books/NBK1431/
url:https://www.ncbi.nlm.nih.gov/pubmed/27376611
is
topic
of
Human Disease Ontology
Faceted Search & Find service v1.17_git144 as of Jul 26 2024
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