@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:NP647569.RAl_ICNcqLfqu9IYry2sD0K47hFwfbK3C0n46lYteITII130_head { this: np:hasAssertion dgn-np:NP647569.RAl_ICNcqLfqu9IYry2sD0K47hFwfbK3C0n46lYteITII130_assertion; np:hasProvenance dgn-np:NP647569.RAl_ICNcqLfqu9IYry2sD0K47hFwfbK3C0n46lYteITII130_provenance; np:hasPublicationInfo dgn-np:NP647569.RAl_ICNcqLfqu9IYry2sD0K47hFwfbK3C0n46lYteITII130_publicationInfo; a np:Nanopublication . dgn-np:NP647569.RAl_ICNcqLfqu9IYry2sD0K47hFwfbK3C0n46lYteITII130_assertion a np:Assertion . dgn-np:NP647569.RAl_ICNcqLfqu9IYry2sD0K47hFwfbK3C0n46lYteITII130_provenance a np:Provenance . dgn-np:NP647569.RAl_ICNcqLfqu9IYry2sD0K47hFwfbK3C0n46lYteITII130_publicationInfo a np:PublicationInfo . } dgn-np:NP647569.RAl_ICNcqLfqu9IYry2sD0K47hFwfbK3C0n46lYteITII130_assertion { miriam-gene:5621 a ncit:C16612 . lld:C0234366 a ncit:C7057 . dgn-gda:DGNb4460dea7722393ac53cd1a2cf18e3f0 sio:SIO_000628 miriam-gene:5621, lld:C0234366; a sio:SIO_001121 . } dgn-np:NP647569.RAl_ICNcqLfqu9IYry2sD0K47hFwfbK3C0n46lYteITII130_provenance { dgn-np:NP647569.RAl_ICNcqLfqu9IYry2sD0K47hFwfbK3C0n46lYteITII130_assertion dcterms:description "[The atypical and rarer variants such as that with dementia of long duration, the ataxic variant, and the variant with kuru plaques were linked to different genotypes at codon 129 and shared the 'type 2' protease-resistant prion protein.]. 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:8651649; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP647569.RAl_ICNcqLfqu9IYry2sD0K47hFwfbK3C0n46lYteITII130_publicationInfo { this: dcterms:created "2015-08-25T14:44:08+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 "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }