@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP189285.RArZXwnOUV0ulnODXNVVI6T2OsF7Ew3L_As8o3abV1Zbc> .
@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:NP189285.RArZXwnOUV0ulnODXNVVI6T2OsF7Ew3L_As8o3abV1Zbc130_head {
   this: np:hasAssertion dgn-np:NP189285.RArZXwnOUV0ulnODXNVVI6T2OsF7Ew3L_As8o3abV1Zbc130_assertion ;
    np:hasProvenance dgn-np:NP189285.RArZXwnOUV0ulnODXNVVI6T2OsF7Ew3L_As8o3abV1Zbc130_provenance ;
    np:hasPublicationInfo dgn-np:NP189285.RArZXwnOUV0ulnODXNVVI6T2OsF7Ew3L_As8o3abV1Zbc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP189285.RArZXwnOUV0ulnODXNVVI6T2OsF7Ew3L_As8o3abV1Zbc130_assertion a np:Assertion .
  dgn-np:NP189285.RArZXwnOUV0ulnODXNVVI6T2OsF7Ew3L_As8o3abV1Zbc130_provenance a np:Provenance .
  dgn-np:NP189285.RArZXwnOUV0ulnODXNVVI6T2OsF7Ew3L_As8o3abV1Zbc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP189285.RArZXwnOUV0ulnODXNVVI6T2OsF7Ew3L_As8o3abV1Zbc130_assertion {
   miriam-gene:118429 a ncit:C16612 .
  lld:C0042769 a ncit:C7057 .
  dgn-gda:DGNdfce715d41a9fc894c1b6ec3da660190 sio:SIO_000628 miriam-gene:118429 , lld:C0042769 ;
    a sio:SIO_001121 .
}
dgn-np:NP189285.RArZXwnOUV0ulnODXNVVI6T2OsF7Ew3L_As8o3abV1Zbc130_provenance {
   dgn-np:NP189285.RArZXwnOUV0ulnODXNVVI6T2OsF7Ew3L_As8o3abV1Zbc130_assertion dcterms:description "[In order to obtain a useful and readily applicable in situ hybridization (ISH) protocol for progressive central nervous system (CNS) diseases of unknown etiology that are possibly due to persistent viral infection, known and well described diseases were studied, namely, progressive multifocal leukoencephalopathy (PML) and subacute sclerosing panencephalitis (SSPE).]. 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:3746947 ;
    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:NP189285.RArZXwnOUV0ulnODXNVVI6T2OsF7Ew3L_As8o3abV1Zbc130_publicationInfo {
   this: dcterms:created "2014-10-02T12:33:44+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" .
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}