@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:NP375054.RAWj41G0xdod7uK_3WJn4TSkqEc8fWHnvJsH6rLZvJY14130_head { this: np:hasAssertion dgn-np:NP375054.RAWj41G0xdod7uK_3WJn4TSkqEc8fWHnvJsH6rLZvJY14130_assertion; np:hasProvenance dgn-np:NP375054.RAWj41G0xdod7uK_3WJn4TSkqEc8fWHnvJsH6rLZvJY14130_provenance; np:hasPublicationInfo dgn-np:NP375054.RAWj41G0xdod7uK_3WJn4TSkqEc8fWHnvJsH6rLZvJY14130_publicationInfo; a np:Nanopublication . dgn-np:NP375054.RAWj41G0xdod7uK_3WJn4TSkqEc8fWHnvJsH6rLZvJY14130_assertion a np:Assertion . dgn-np:NP375054.RAWj41G0xdod7uK_3WJn4TSkqEc8fWHnvJsH6rLZvJY14130_provenance a np:Provenance . dgn-np:NP375054.RAWj41G0xdod7uK_3WJn4TSkqEc8fWHnvJsH6rLZvJY14130_publicationInfo a np:PublicationInfo . } dgn-np:NP375054.RAWj41G0xdod7uK_3WJn4TSkqEc8fWHnvJsH6rLZvJY14130_assertion { miriam-gene:2026 a ncit:C16612 . lld:C0004134 a ncit:C7057 . dgn-gda:DGN6556825f90752bdc2b76dba48c5fef26 sio:SIO_000628 miriam-gene:2026, lld:C0004134; a sio:SIO_001121 . } dgn-np:NP375054.RAWj41G0xdod7uK_3WJn4TSkqEc8fWHnvJsH6rLZvJY14130_provenance { dgn-np:NP375054.RAWj41G0xdod7uK_3WJn4TSkqEc8fWHnvJsH6rLZvJY14130_assertion dcterms:description "[A 68 year old woman with sporadic Creutzfeldt-Jakob disease is described, who neither showed characteristic EEG abnormalities nor a positive test of the neuronal protein 14-3-3 or neuron specific enolase (NSE) in CSF, despite a clinical presentation with ataxia of cerebellar type, rapidly progressive dementia, myoclonus, and marked hyperintense signal abnormalities in the deep cortical layers and the basal ganglia on T2 and diffusion weighted MRI.]. 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:10519881; 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:NP375054.RAWj41G0xdod7uK_3WJn4TSkqEc8fWHnvJsH6rLZvJY14130_publicationInfo { this: dcterms:created "2015-08-25T14:41:16+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" . }