@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP336926.RAZsfOGKw9h_OlhLuYdhRuvfW8CYf6rHad1zePMIb1Rzc> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP336926.RAZsfOGKw9h_OlhLuYdhRuvfW8CYf6rHad1zePMIb1Rzc130_head {
  this: np:hasAssertion dgn-np:NP336926.RAZsfOGKw9h_OlhLuYdhRuvfW8CYf6rHad1zePMIb1Rzc130_assertion;
    np:hasProvenance dgn-np:NP336926.RAZsfOGKw9h_OlhLuYdhRuvfW8CYf6rHad1zePMIb1Rzc130_provenance;
    np:hasPublicationInfo dgn-np:NP336926.RAZsfOGKw9h_OlhLuYdhRuvfW8CYf6rHad1zePMIb1Rzc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP336926.RAZsfOGKw9h_OlhLuYdhRuvfW8CYf6rHad1zePMIb1Rzc130_assertion a np:Assertion .
  
  dgn-np:NP336926.RAZsfOGKw9h_OlhLuYdhRuvfW8CYf6rHad1zePMIb1Rzc130_provenance a np:Provenance .
  
  dgn-np:NP336926.RAZsfOGKw9h_OlhLuYdhRuvfW8CYf6rHad1zePMIb1Rzc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP336926.RAZsfOGKw9h_OlhLuYdhRuvfW8CYf6rHad1zePMIb1Rzc130_assertion {
  miriam-gene:19 a ncit:C16612 .
  
  lld:C2931838 a ncit:C7057 .
  
  dgn-gda:DGN4859c6ec3abafbad82ca640a82790bc7 sio:SIO_000628 miriam-gene:19, lld:C2931838;
    a sio:SIO_001121 .
}

dgn-np:NP336926.RAZsfOGKw9h_OlhLuYdhRuvfW8CYf6rHad1zePMIb1Rzc130_provenance {
  dgn-np:NP336926.RAZsfOGKw9h_OlhLuYdhRuvfW8CYf6rHad1zePMIb1Rzc130_assertion dcterms:description
      "[The identification of mutations in ABCA1 in patients with Tangier disease and familial HDL deficiency demonstrated that inadequate transport of phospholipid and cholesterol to the extracellular space results in the hypercatabolism of lipid-poor nascent HDL particles.]. 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:11714841;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP336926.RAZsfOGKw9h_OlhLuYdhRuvfW8CYf6rHad1zePMIb1Rzc130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:18+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}