@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:NP401121.RAhii9VCnJugmKcPnMTUmUpZXRj8UEF3CpsLGDj5A1OWs130_head { this: np:hasAssertion dgn-np:NP401121.RAhii9VCnJugmKcPnMTUmUpZXRj8UEF3CpsLGDj5A1OWs130_assertion; np:hasProvenance dgn-np:NP401121.RAhii9VCnJugmKcPnMTUmUpZXRj8UEF3CpsLGDj5A1OWs130_provenance; np:hasPublicationInfo dgn-np:NP401121.RAhii9VCnJugmKcPnMTUmUpZXRj8UEF3CpsLGDj5A1OWs130_publicationInfo; a np:Nanopublication . dgn-np:NP401121.RAhii9VCnJugmKcPnMTUmUpZXRj8UEF3CpsLGDj5A1OWs130_assertion a np:Assertion . dgn-np:NP401121.RAhii9VCnJugmKcPnMTUmUpZXRj8UEF3CpsLGDj5A1OWs130_provenance a np:Provenance . dgn-np:NP401121.RAhii9VCnJugmKcPnMTUmUpZXRj8UEF3CpsLGDj5A1OWs130_publicationInfo a np:PublicationInfo . } dgn-np:NP401121.RAhii9VCnJugmKcPnMTUmUpZXRj8UEF3CpsLGDj5A1OWs130_assertion { miriam-gene:5621 a ncit:C16612 . lld:C0022336 a ncit:C7057 . dgn-gda:DGN6e2bfed41d4dcc702a3d4d8d5ffcee3a sio:SIO_000628 miriam-gene:5621, lld:C0022336; a sio:SIO_001122 . } dgn-np:NP401121.RAhii9VCnJugmKcPnMTUmUpZXRj8UEF3CpsLGDj5A1OWs130_provenance { dgn-np:NP401121.RAhii9VCnJugmKcPnMTUmUpZXRj8UEF3CpsLGDj5A1OWs130_assertion dcterms:description "[Accumulation of an isoform of protease-resistant PrP fragment in FFI distinct from that found in a familial form of Creutzfeldt-Jakob disease with the same D178N mutation, shows the effect of the polymorphism at codon 129 of PRNP on phenotypic expression and the possibility of distinct prion strains with diverse pathological potential.]. 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:12849238; 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:NP401121.RAhii9VCnJugmKcPnMTUmUpZXRj8UEF3CpsLGDj5A1OWs130_publicationInfo { this: dcterms:created "2016-05-13T12:44:47+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" . }