Document
type: Class

Academic Article
type: Class

Continuant
type: Class

Entity
type: Class

456233408
type: Entity
type: BFO_0000020
type: Authorship
type: Relationship
type: Continuant
type: Thing
relates: Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome

Generically Dependent Continuant
type: Class

Article
type: Class

456233452
type: Entity
type: BFO_0000020
type: Authorship
type: Relationship
type: Continuant
type: Thing
relates: Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome

456233474
type: Entity
type: BFO_0000020
type: Authorship
type: Relationship
type: Continuant
type: Thing
relates: Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome

Inglese
type: Language

RDF description of Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome - http://irises.unipv.it/resource/item/554422
rights: termsOfUse
date: 2026-08-24T09:19:47
publisher: Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome
type: Document

456233553
type: Entity
type: BFO_0000020
type: Authorship
type: Relationship
type: Continuant
type: Thing
relates: Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome

Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome
type: Continuant
type: Document
type: Article
related by: 456233553
type: Academic Article
type: Entity
related by: 456233452
language: Inglese
type: Thing
type: Generically Dependent Continuant
related by: 456233408
most specific type: Academic Article
related by: 456233474
type: Information Content Entity

Information Content Entity
type: Class