@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP420745.RAK0bbLC6jDRE_Cv0758a1V38eSqFdihLPIuwdDlhj7r8> .
@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:NP420745.RAK0bbLC6jDRE_Cv0758a1V38eSqFdihLPIuwdDlhj7r8130_head {
  this: np:hasAssertion dgn-np:NP420745.RAK0bbLC6jDRE_Cv0758a1V38eSqFdihLPIuwdDlhj7r8130_assertion;
    np:hasProvenance dgn-np:NP420745.RAK0bbLC6jDRE_Cv0758a1V38eSqFdihLPIuwdDlhj7r8130_provenance;
    np:hasPublicationInfo dgn-np:NP420745.RAK0bbLC6jDRE_Cv0758a1V38eSqFdihLPIuwdDlhj7r8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP420745.RAK0bbLC6jDRE_Cv0758a1V38eSqFdihLPIuwdDlhj7r8130_assertion a np:Assertion .
  
  dgn-np:NP420745.RAK0bbLC6jDRE_Cv0758a1V38eSqFdihLPIuwdDlhj7r8130_provenance a np:Provenance .
  
  dgn-np:NP420745.RAK0bbLC6jDRE_Cv0758a1V38eSqFdihLPIuwdDlhj7r8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP420745.RAK0bbLC6jDRE_Cv0758a1V38eSqFdihLPIuwdDlhj7r8130_assertion {
  miriam-gene:1583 a ncit:C16612 .
  
  lld:C0342492 a ncit:C7057 .
  
  dgn-gda:DGN7618fdbe233c8ca2da34ec685be0b5cf sio:SIO_000628 miriam-gene:1583, lld:C0342492;
    a sio:SIO_001121 .
}

dgn-np:NP420745.RAK0bbLC6jDRE_Cv0758a1V38eSqFdihLPIuwdDlhj7r8130_provenance {
  dgn-np:NP420745.RAK0bbLC6jDRE_Cv0758a1V38eSqFdihLPIuwdDlhj7r8130_assertion dcterms:description
      "[These studies show that lipoid CAH is not caused by lesions in the P450scc gene, and suggest that another unidentified factor is required for the conversion of cholesterol to pregnenolone, and is disordered in congenital lipoid adrenal hyperplasia.]. 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:1661294;
    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:NP420745.RAK0bbLC6jDRE_Cv0758a1V38eSqFdihLPIuwdDlhj7r8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:09+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" .
}