Document
type: Class

Academic Article
type: Class

Continuant
type: Class

1569808
type: Entity
type: BFO_0000020
type: Authorship
type: Relationship
type: Continuant
type: Thing
relates: Mutations in the MCFD2 gene are predominant among patients with hereditary combined FV and FVIII deficiency (F5F8D) in India

Entity
type: Class

Mutations in the MCFD2 gene are predominant among patients with hereditary combined FV and FVIII deficiency (F5F8D) in India
related by: 1569808
type: Article
most specific type: Academic Article
type: Document
type: Information Content Entity
type: Thing
type: Academic Article
type: Continuant
language: English
type: Entity
type: Generically Dependent Continuant

Generically Dependent Continuant
type: Class

Article
type: Class

English
type: Language

Information Content Entity
type: Class

RDF description of Mutations in the MCFD2 gene are predominant among patients with hereditary combined FV and FVIII deficiency (F5F8D) in India - http://irises.unimi.it/resource/item/103135
rights: termsOfUse
date: 2026-08-04T02:17:42
publisher: Mutations in the MCFD2 gene are predominant among patients with hereditary combined FV and FVIII deficiency (F5F8D) in India
type: Document