@prefix this: . @prefix sub: . @prefix has-source: . @prefix refers-to: . @prefix gene-disease-association: . @prefix xsd: . @prefix dcterms: . @prefix np: . @prefix wd: . @prefix prov: . @prefix pmid: . @prefix pav: . @prefix ensembl: . @prefix omim: . @prefix ncit: . @prefix orcid: . @prefix rdfs: . sub:head { this: np:hasAssertion sub:assertion; np:hasProvenance sub:provenance; np:hasPublicationInfo sub:publicationInfo; a np:Nanopublication . } sub:assertion { ensembl:ENSG00000282307 a ncit:C16612; rdfs:label "SERPINF1" . sub:association refers-to: ensembl:ENSG00000282307, omim:613982; a gene-disease-association: . } sub:provenance { pmid:21353196 dcterms:title "Exome sequencing identifies truncating mutations in human SERPINF1 in autosomal-recessive osteogenesis imperfecta" . sub:assertion has-source: pmid:21353196 . } sub:publicationInfo { sub:activity a prov:Activity; prov:atLocation wd:Q1137652 . this: dcterms:created "2018-04-05T10:17:11.353+02:00"^^xsd:dateTime; dcterms:rights ; pav:authoredBy orcid:0000-0001-6048-1457, orcid:0000-0002-7770-620X; pav:createdBy orcid:0000-0001-7542-0286; prov:wasGeneratedBy sub:activity . }