@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:NP703082.RAOD6eorp2pgAMjlb97rtdNuoyzneJftAaqUy855tC-ng130_head { this: np:hasAssertion dgn-np:NP703082.RAOD6eorp2pgAMjlb97rtdNuoyzneJftAaqUy855tC-ng130_assertion; np:hasProvenance dgn-np:NP703082.RAOD6eorp2pgAMjlb97rtdNuoyzneJftAaqUy855tC-ng130_provenance; np:hasPublicationInfo dgn-np:NP703082.RAOD6eorp2pgAMjlb97rtdNuoyzneJftAaqUy855tC-ng130_publicationInfo; a np:Nanopublication . dgn-np:NP703082.RAOD6eorp2pgAMjlb97rtdNuoyzneJftAaqUy855tC-ng130_assertion a np:Assertion . dgn-np:NP703082.RAOD6eorp2pgAMjlb97rtdNuoyzneJftAaqUy855tC-ng130_provenance a np:Provenance . dgn-np:NP703082.RAOD6eorp2pgAMjlb97rtdNuoyzneJftAaqUy855tC-ng130_publicationInfo a np:PublicationInfo . } dgn-np:NP703082.RAOD6eorp2pgAMjlb97rtdNuoyzneJftAaqUy855tC-ng130_assertion { miriam-gene:5621 a ncit:C16612 . lld:C2931859 a ncit:C7057 . dgn-gda:DGN03070e1b4f445e006b12e6232ee67598 sio:SIO_000628 miriam-gene:5621, lld:C2931859; a sio:SIO_001121 . } dgn-np:NP703082.RAOD6eorp2pgAMjlb97rtdNuoyzneJftAaqUy855tC-ng130_provenance { dgn-np:NP703082.RAOD6eorp2pgAMjlb97rtdNuoyzneJftAaqUy855tC-ng130_assertion dcterms:description "[We have compared clinicpathological patient profiles including geographic and gender distribution, age at disease onset, duration of disease, clinical symptoms, and recognized or hypothetical risk factors for CJD, genetic risk factors, biochemical and histopathological data for two cohorts of Swiss sporadic CJD patients from years of regular sporadic CJD incidence (1996-2000, mean incidence 1.3 cases/10(6) inhabitants, n = 47) to Swiss sporadic CJD patients from years of elevated sporadic CJD incidence (2001-2004, mean incidence 2.3 cases/10(6) inhabitants, n = 73).]. 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:19005626; 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:NP703082.RAOD6eorp2pgAMjlb97rtdNuoyzneJftAaqUy855tC-ng130_publicationInfo { this: dcterms:created "2016-05-13T12:47:03+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" . }