@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP423136.RAHjt83W_u_aWl1AxkeI18DXkFmxEur4uSVHE_DVXcBZk> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP423136.RAHjt83W_u_aWl1AxkeI18DXkFmxEur4uSVHE_DVXcBZk130_head {
  this: np:hasAssertion dgn-np:NP423136.RAHjt83W_u_aWl1AxkeI18DXkFmxEur4uSVHE_DVXcBZk130_assertion;
    np:hasProvenance dgn-np:NP423136.RAHjt83W_u_aWl1AxkeI18DXkFmxEur4uSVHE_DVXcBZk130_provenance;
    np:hasPublicationInfo dgn-np:NP423136.RAHjt83W_u_aWl1AxkeI18DXkFmxEur4uSVHE_DVXcBZk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP423136.RAHjt83W_u_aWl1AxkeI18DXkFmxEur4uSVHE_DVXcBZk130_assertion a np:Assertion .
  
  dgn-np:NP423136.RAHjt83W_u_aWl1AxkeI18DXkFmxEur4uSVHE_DVXcBZk130_provenance a np:Provenance .
  
  dgn-np:NP423136.RAHjt83W_u_aWl1AxkeI18DXkFmxEur4uSVHE_DVXcBZk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP423136.RAHjt83W_u_aWl1AxkeI18DXkFmxEur4uSVHE_DVXcBZk130_assertion {
  miriam-gene:3918 a ncit:C16612 .
  
  lld:C2921627 a ncit:C7057 .
  
  dgn-gda:DGN5c9d4c2710f023184b5f630a8fd6b84d sio:SIO_000628 miriam-gene:3918, lld:C2921627;
    a sio:SIO_001121 .
}

dgn-np:NP423136.RAHjt83W_u_aWl1AxkeI18DXkFmxEur4uSVHE_DVXcBZk130_provenance {
  dgn-np:NP423136.RAHjt83W_u_aWl1AxkeI18DXkFmxEur4uSVHE_DVXcBZk130_assertion dcterms:description
      "[The prevalence of JCV DNA was analyzed in CSF and plasma from 217 patients with MS, 86 patients with clinically isolated syndrome (CIS), and 212 patients with other neurological diseases (OND).]. 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:18805840;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP423136.RAHjt83W_u_aWl1AxkeI18DXkFmxEur4uSVHE_DVXcBZk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:11+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
      <http://orcid.org/0000-0002-9383-528X>, <http://orcid.org/0000-0003-0169-8159>, <http://orcid.org/0000-0003-1244-7654>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}