Document
type: Class

483232360
type: Entity
type: BFO_0000020
type: Authorship
type: Relationship
type: Continuant
type: Thing
relates: Bi-allelic variants in FSD1L cause a neurodevelopmental disorder overlapping with L1 syndrome

Academic Article
type: Class

Continuant
type: Class

Entity
type: Class

Generically Dependent Continuant
type: Class

Article
type: Class

Inglese
type: Language

483232318
type: Entity
type: BFO_0000020
type: Authorship
type: Relationship
type: Continuant
type: Thing
relates: Bi-allelic variants in FSD1L cause a neurodevelopmental disorder overlapping with L1 syndrome

RDF description of Bi-allelic variants in FSD1L cause a neurodevelopmental disorder overlapping with L1 syndrome - http://irises.unipv.it/resource/item/618916
rights: termsOfUse
date: 2026-08-24T09:19:45
publisher: Bi-allelic variants in FSD1L cause a neurodevelopmental disorder overlapping with L1 syndrome
type: Document

Information Content Entity
type: Class

483232347
type: Entity
type: BFO_0000020
type: Authorship
type: Relationship
type: Continuant
type: Thing
relates: Bi-allelic variants in FSD1L cause a neurodevelopmental disorder overlapping with L1 syndrome

483232324
type: Entity
type: BFO_0000020
type: Authorship
type: Relationship
type: Continuant
type: Thing
relates: Bi-allelic variants in FSD1L cause a neurodevelopmental disorder overlapping with L1 syndrome

Bi-allelic variants in FSD1L cause a neurodevelopmental disorder overlapping with L1 syndrome
related by: 483232347
most specific type: Academic Article
related by: 483232318
type: Document
related by: 483232360
language: Inglese
type: Article
type: Generically Dependent Continuant
type: Entity
type: Thing
related by: 483232324
type: Information Content Entity
type: Academic Article
type: Continuant