@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP1321186.RAIVjKVvTeA_7HChaLSYJwDWlY_XqsLecsyc2RYE8yjH4130_head { this: np:hasAssertion dgn-np:NP1321186.RAIVjKVvTeA_7HChaLSYJwDWlY_XqsLecsyc2RYE8yjH4130_assertion; np:hasProvenance dgn-np:NP1321186.RAIVjKVvTeA_7HChaLSYJwDWlY_XqsLecsyc2RYE8yjH4130_provenance; np:hasPublicationInfo dgn-np:NP1321186.RAIVjKVvTeA_7HChaLSYJwDWlY_XqsLecsyc2RYE8yjH4130_publicationInfo; a np:Nanopublication . dgn-np:NP1321186.RAIVjKVvTeA_7HChaLSYJwDWlY_XqsLecsyc2RYE8yjH4130_assertion a np:Assertion . dgn-np:NP1321186.RAIVjKVvTeA_7HChaLSYJwDWlY_XqsLecsyc2RYE8yjH4130_provenance a np:Provenance . dgn-np:NP1321186.RAIVjKVvTeA_7HChaLSYJwDWlY_XqsLecsyc2RYE8yjH4130_publicationInfo a np:PublicationInfo . } dgn-np:NP1321186.RAIVjKVvTeA_7HChaLSYJwDWlY_XqsLecsyc2RYE8yjH4130_assertion { miriam-gene:5621 a ncit:C16612 . lld:C0206042 a ncit:C7057 . dgn-gda:DGN01c2d462f07b9a62a007bb28009d6e3e sio:SIO_000628 miriam-gene:5621, lld:C0206042; a sio:SIO_001121 . } dgn-np:NP1321186.RAIVjKVvTeA_7HChaLSYJwDWlY_XqsLecsyc2RYE8yjH4130_provenance { dgn-np:NP1321186.RAIVjKVvTeA_7HChaLSYJwDWlY_XqsLecsyc2RYE8yjH4130_assertion dcterms:description "[The comparative study of PrPres distribution in FFI homozygotes and heterozygotes at codon 129 has lead to the conclusion that the phenotypic differences observed between these two FFI patient populations may be the result of different rates of conversion of normal PrP into PrPres, at least in some brain regions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en; wi:evidence dgn-void:source_evidence_literature; sio:SIO_000772 miriam-pubmed:7767490; prov:wasDerivedFrom dgn-void:befree-2016; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-2016 pav:importedOn "2016-02-19"^^xsd:date . dgn-void:source_evidence_literature a eco:ECO_0000212; rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en; rdfs:label "DisGeNET evidence - LITERATURE"@en . } dgn-np:NP1321186.RAIVjKVvTeA_7HChaLSYJwDWlY_XqsLecsyc2RYE8yjH4130_publicationInfo { this: dcterms:created "2016-05-13T12:51:45+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }