@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP669914.RAc1VKdiNgPwdQO2ObCLzdOBczPnanlTGjicF4_yrhNtA> .
@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:NP669914.RAc1VKdiNgPwdQO2ObCLzdOBczPnanlTGjicF4_yrhNtA130_head {
  this: np:hasAssertion dgn-np:NP669914.RAc1VKdiNgPwdQO2ObCLzdOBczPnanlTGjicF4_yrhNtA130_assertion;
    np:hasProvenance dgn-np:NP669914.RAc1VKdiNgPwdQO2ObCLzdOBczPnanlTGjicF4_yrhNtA130_provenance;
    np:hasPublicationInfo dgn-np:NP669914.RAc1VKdiNgPwdQO2ObCLzdOBczPnanlTGjicF4_yrhNtA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP669914.RAc1VKdiNgPwdQO2ObCLzdOBczPnanlTGjicF4_yrhNtA130_assertion a np:Assertion .
  
  dgn-np:NP669914.RAc1VKdiNgPwdQO2ObCLzdOBczPnanlTGjicF4_yrhNtA130_provenance a np:Provenance .
  
  dgn-np:NP669914.RAc1VKdiNgPwdQO2ObCLzdOBczPnanlTGjicF4_yrhNtA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP669914.RAc1VKdiNgPwdQO2ObCLzdOBczPnanlTGjicF4_yrhNtA130_assertion {
  miriam-gene:5251 a ncit:C16612 .
  
  lld:C0043459 a ncit:C7057 .
  
  dgn-gda:DGN7383e9595af3a8b776fd5afd017078be sio:SIO_000628 miriam-gene:5251, lld:C0043459;
    a sio:SIO_001121 .
}

dgn-np:NP669914.RAc1VKdiNgPwdQO2ObCLzdOBczPnanlTGjicF4_yrhNtA130_provenance {
  dgn-np:NP669914.RAc1VKdiNgPwdQO2ObCLzdOBczPnanlTGjicF4_yrhNtA130_assertion dcterms:description
      "[To exclude that genetic differences, resulting in different defects in peroxisomal biogenesis, have differential effects on the activity of the cholesterol biosynthetic enzymes and on de novo cholesterol biosynthesis, we chose fibroblasts of patients with defined defects in one of four different PEX genes leading to Zellweger syndrome (PEX1, PEX5, PEX16 or PEX19).]. 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:14680974;
    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:NP669914.RAc1VKdiNgPwdQO2ObCLzdOBczPnanlTGjicF4_yrhNtA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:44+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" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}