@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:NP531327.RASbIFnJt9xv7meyq3ukaEsdq9CkQMqn0MrdUaKSbJt8M130_head { this: np:hasAssertion dgn-np:NP531327.RASbIFnJt9xv7meyq3ukaEsdq9CkQMqn0MrdUaKSbJt8M130_assertion; np:hasProvenance dgn-np:NP531327.RASbIFnJt9xv7meyq3ukaEsdq9CkQMqn0MrdUaKSbJt8M130_provenance; np:hasPublicationInfo dgn-np:NP531327.RASbIFnJt9xv7meyq3ukaEsdq9CkQMqn0MrdUaKSbJt8M130_publicationInfo; a np:Nanopublication . dgn-np:NP531327.RASbIFnJt9xv7meyq3ukaEsdq9CkQMqn0MrdUaKSbJt8M130_assertion a np:Assertion . dgn-np:NP531327.RASbIFnJt9xv7meyq3ukaEsdq9CkQMqn0MrdUaKSbJt8M130_provenance a np:Provenance . dgn-np:NP531327.RASbIFnJt9xv7meyq3ukaEsdq9CkQMqn0MrdUaKSbJt8M130_publicationInfo a np:PublicationInfo . } dgn-np:NP531327.RASbIFnJt9xv7meyq3ukaEsdq9CkQMqn0MrdUaKSbJt8M130_assertion { miriam-gene:3918 a ncit:C16612 . lld:C2931859 a ncit:C7057 . dgn-gda:DGN6a77e52cd111502abaf089ac4af45ae1 sio:SIO_000628 miriam-gene:3918, lld:C2931859; a sio:SIO_001121 . } dgn-np:NP531327.RASbIFnJt9xv7meyq3ukaEsdq9CkQMqn0MrdUaKSbJt8M130_provenance { dgn-np:NP531327.RASbIFnJt9xv7meyq3ukaEsdq9CkQMqn0MrdUaKSbJt8M130_assertion dcterms:description "[Moreover, our results from combining frequencies of two HERV families indicated that the prevalence of many combination groups was significantly different between sporadic CJD and normal CSF samples and between two patients' CSF samples.]. 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:20005155; 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:NP531327.RASbIFnJt9xv7meyq3ukaEsdq9CkQMqn0MrdUaKSbJt8M130_publicationInfo { this: dcterms:created "2015-08-25T14:42:54+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" . }