@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP53147.RAWbLZZME52Aw2cHKBsWcgozScBEchH4mv4KeixlBGJ20> .
@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:NP53147.RAWbLZZME52Aw2cHKBsWcgozScBEchH4mv4KeixlBGJ20130_head {
  this: np:hasAssertion dgn-np:NP53147.RAWbLZZME52Aw2cHKBsWcgozScBEchH4mv4KeixlBGJ20130_assertion;
    np:hasProvenance dgn-np:NP53147.RAWbLZZME52Aw2cHKBsWcgozScBEchH4mv4KeixlBGJ20130_provenance;
    np:hasPublicationInfo dgn-np:NP53147.RAWbLZZME52Aw2cHKBsWcgozScBEchH4mv4KeixlBGJ20130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP53147.RAWbLZZME52Aw2cHKBsWcgozScBEchH4mv4KeixlBGJ20130_assertion a np:Assertion .
  
  dgn-np:NP53147.RAWbLZZME52Aw2cHKBsWcgozScBEchH4mv4KeixlBGJ20130_provenance a np:Provenance .
  
  dgn-np:NP53147.RAWbLZZME52Aw2cHKBsWcgozScBEchH4mv4KeixlBGJ20130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP53147.RAWbLZZME52Aw2cHKBsWcgozScBEchH4mv4KeixlBGJ20130_assertion {
  miriam-gene:65018 a ncit:C16612 .
  
  lld:C0030567 a ncit:C7057 .
  
  dgn-gda:DGN93068f9714e944f4561beb36d48b84e9 sio:SIO_000628 miriam-gene:65018, lld:C0030567;
    a sio:SIO_001122 .
}

dgn-np:NP53147.RAWbLZZME52Aw2cHKBsWcgozScBEchH4mv4KeixlBGJ20130_provenance {
  dgn-np:NP53147.RAWbLZZME52Aw2cHKBsWcgozScBEchH4mv4KeixlBGJ20130_assertion dcterms:description
      "[The relative contribution of simple mutations and copy number variations (CNVs) in SNCA, PARK2, PINK1, PARK7, and LRRK2 to the genetic etiology of Parkinson disease (PD) is still unclear because most studies did not completely analyze each gene.]. 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:19405094;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP53147.RAWbLZZME52Aw2cHKBsWcgozScBEchH4mv4KeixlBGJ20130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:24+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" .
}