@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP729954.RAloxa1uVWkNHNjddToJAFMm6KnGZbR8CynNx07UlxPRg> .
@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:NP729954.RAloxa1uVWkNHNjddToJAFMm6KnGZbR8CynNx07UlxPRg130_head {
  this: np:hasAssertion dgn-np:NP729954.RAloxa1uVWkNHNjddToJAFMm6KnGZbR8CynNx07UlxPRg130_assertion ;
    np:hasProvenance dgn-np:NP729954.RAloxa1uVWkNHNjddToJAFMm6KnGZbR8CynNx07UlxPRg130_provenance ;
    np:hasPublicationInfo dgn-np:NP729954.RAloxa1uVWkNHNjddToJAFMm6KnGZbR8CynNx07UlxPRg130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP729954.RAloxa1uVWkNHNjddToJAFMm6KnGZbR8CynNx07UlxPRg130_provenance a np:Provenance .
  dgn-np:NP729954.RAloxa1uVWkNHNjddToJAFMm6KnGZbR8CynNx07UlxPRg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP729954.RAloxa1uVWkNHNjddToJAFMm6KnGZbR8CynNx07UlxPRg130_assertion {
  miriam-gene:118429 a ncit:C16612 .
  lld:C0038522 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP729954.RAloxa1uVWkNHNjddToJAFMm6KnGZbR8CynNx07UlxPRg130_provenance {
  dgn-np:NP729954.RAloxa1uVWkNHNjddToJAFMm6KnGZbR8CynNx07UlxPRg130_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 ;
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    prov:wasDerivedFrom dgn-void:befree-20140225 ;
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  dgn-void:source_evidence_literature a eco:ECO_0000212 ;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
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}
dgn-np:NP729954.RAloxa1uVWkNHNjddToJAFMm6KnGZbR8CynNx07UlxPRg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:23+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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