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An Entity of Type : owl:Axiom, within Data Space : linkeddata.uriburner.com:28898 associated with source document(s)

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
annotatedProperty	http://purl.obolibrary.org/obo/IAO_0000115
annotatedSource	nonsyndromic congenital nail disorder 4
annotatedTarget	A nonsyndromic congenital nail disorder that is characterized by complete absence or severe hypoplasia of all fingernails and toenails without significant bone anomalies, and that has_material_basis_in homozygous or compound heterozygous mutation in the R-spondin-4 gene on chromosome 20p13.
database_cross_reference	url:https://pubmed.ncbi.nlm.nih.gov/26149975/ url:https://ghr.nlm.nih.gov/condition/anonychia-congenita
is topic of	Human Disease Ontology

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