@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP266266.RAPNL8BH2BbATMQ30VewKSxcHk90e3tWRmhzfZLB0Oq70> .
@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:NP266266.RAPNL8BH2BbATMQ30VewKSxcHk90e3tWRmhzfZLB0Oq70130_head {
  this: np:hasAssertion dgn-np:NP266266.RAPNL8BH2BbATMQ30VewKSxcHk90e3tWRmhzfZLB0Oq70130_assertion;
    np:hasProvenance dgn-np:NP266266.RAPNL8BH2BbATMQ30VewKSxcHk90e3tWRmhzfZLB0Oq70130_provenance;
    np:hasPublicationInfo dgn-np:NP266266.RAPNL8BH2BbATMQ30VewKSxcHk90e3tWRmhzfZLB0Oq70130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP266266.RAPNL8BH2BbATMQ30VewKSxcHk90e3tWRmhzfZLB0Oq70130_assertion a np:Assertion .
  
  dgn-np:NP266266.RAPNL8BH2BbATMQ30VewKSxcHk90e3tWRmhzfZLB0Oq70130_provenance a np:Provenance .
  
  dgn-np:NP266266.RAPNL8BH2BbATMQ30VewKSxcHk90e3tWRmhzfZLB0Oq70130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP266266.RAPNL8BH2BbATMQ30VewKSxcHk90e3tWRmhzfZLB0Oq70130_assertion {
  miriam-gene:28982 a ncit:C16612 .
  
  lld:C0030567 a ncit:C7057 .
  
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    a sio:SIO_001121 .
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dgn-np:NP266266.RAPNL8BH2BbATMQ30VewKSxcHk90e3tWRmhzfZLB0Oq70130_provenance {
  dgn-np:NP266266.RAPNL8BH2BbATMQ30VewKSxcHk90e3tWRmhzfZLB0Oq70130_assertion dcterms:description
      "[Distribution plots and PCA mapping enabled removal of several outliers out of the 105 analyzed PD and control samples, which improved the discriminative power for PD blood cells compared to healthy and neurological disease controls.]. 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:18692253;
    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:NP266266.RAPNL8BH2BbATMQ30VewKSxcHk90e3tWRmhzfZLB0Oq70130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:28+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>,
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  dgn-void:disgenetrdf pav:version "v2.1.0" .
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