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?:definition
  • An autosomal recessive, inherited coagulation disorder characterized by the partial or complete absence of fibrinogen (factor I) activity in the blood.
?:hasCUIAnnotation
?:hasGeneratedBy
?:type

Metadata

Anon_0  
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<http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://www.w3.org/2004/03/trix/rdfg-1/Graph>
<http://xmlns.com/foaf/0.1/primaryTopic> <https://research.tib.eu/covid-19/entity/C0019250_NCI_NICHD>
<http://xmlns.com/foaf/0.1/topic> Anon_0
<http://www.ontologydesignpatterns.org/cp/owl/informationrealization.owl#realizes> <https://research.tib.eu/covid-19/data/entity/C0019250_NCI_NICHD>
<http://purl.org/net/provenance/ns#createdBy>
Anon_1   (more)
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