@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP532298.RAnCR63jRM9_VeVWLfatmYdBufnL9D0IgnhDVOgUZsbaI> .
@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/v3.0.0/void/> .

dgn-np:NP532298.RAnCR63jRM9_VeVWLfatmYdBufnL9D0IgnhDVOgUZsbaI130_head {
  this: np:hasAssertion dgn-np:NP532298.RAnCR63jRM9_VeVWLfatmYdBufnL9D0IgnhDVOgUZsbaI130_assertion;
    np:hasProvenance dgn-np:NP532298.RAnCR63jRM9_VeVWLfatmYdBufnL9D0IgnhDVOgUZsbaI130_provenance;
    np:hasPublicationInfo dgn-np:NP532298.RAnCR63jRM9_VeVWLfatmYdBufnL9D0IgnhDVOgUZsbaI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP532298.RAnCR63jRM9_VeVWLfatmYdBufnL9D0IgnhDVOgUZsbaI130_assertion a np:Assertion .
  
  dgn-np:NP532298.RAnCR63jRM9_VeVWLfatmYdBufnL9D0IgnhDVOgUZsbaI130_provenance a np:Provenance .
  
  dgn-np:NP532298.RAnCR63jRM9_VeVWLfatmYdBufnL9D0IgnhDVOgUZsbaI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP532298.RAnCR63jRM9_VeVWLfatmYdBufnL9D0IgnhDVOgUZsbaI130_assertion {
  miriam-gene:3931 a ncit:C16612 .
  
  lld:C0010068 a ncit:C7057 .
  
  dgn-gda:DGNf0575ec1cbcf00874ca08130090cbf34 sio:SIO_000628 miriam-gene:3931, lld:C0010068;
    a sio:SIO_001121 .
}

dgn-np:NP532298.RAnCR63jRM9_VeVWLfatmYdBufnL9D0IgnhDVOgUZsbaI130_provenance {
  dgn-np:NP532298.RAnCR63jRM9_VeVWLfatmYdBufnL9D0IgnhDVOgUZsbaI130_assertion dcterms:description
      "[To examine the recent advances in our knowledge of HDL metabolism, composition, function, and coronary heart disease (CHD), as well as marked HDL deficiency states because of mutations in the apolipoprotein (apo) A-I, ATP-binding cassette transfer protein A1 and lecithin cholesterol acyltransferase (LCAT) gene loci.]. 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:24785961;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP532298.RAnCR63jRM9_VeVWLfatmYdBufnL9D0IgnhDVOgUZsbaI130_publicationInfo {
  this: dcterms:created "2015-08-25T14:42:54+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}