@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1267486.RAEQoCW2J56rqm3Ykv_RGlPNcpWfQjOkFugeG1AapqRBk> .
@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:NP1267486.RAEQoCW2J56rqm3Ykv_RGlPNcpWfQjOkFugeG1AapqRBk130_head {
  this: np:hasAssertion dgn-np:NP1267486.RAEQoCW2J56rqm3Ykv_RGlPNcpWfQjOkFugeG1AapqRBk130_assertion;
    np:hasProvenance dgn-np:NP1267486.RAEQoCW2J56rqm3Ykv_RGlPNcpWfQjOkFugeG1AapqRBk130_provenance;
    np:hasPublicationInfo dgn-np:NP1267486.RAEQoCW2J56rqm3Ykv_RGlPNcpWfQjOkFugeG1AapqRBk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1267486.RAEQoCW2J56rqm3Ykv_RGlPNcpWfQjOkFugeG1AapqRBk130_assertion a np:Assertion .
  
  dgn-np:NP1267486.RAEQoCW2J56rqm3Ykv_RGlPNcpWfQjOkFugeG1AapqRBk130_provenance a np:Provenance .
  
  dgn-np:NP1267486.RAEQoCW2J56rqm3Ykv_RGlPNcpWfQjOkFugeG1AapqRBk130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1267486.RAEQoCW2J56rqm3Ykv_RGlPNcpWfQjOkFugeG1AapqRBk130_assertion {
  miriam-gene:348 a ncit:C16612 .
  
  lld:C0020445 a ncit:C7057 .
  
  dgn-gda:DGN5492bbe98d9da265a1a70162884e153f sio:SIO_000628 miriam-gene:348, lld:C0020445;
    a sio:SIO_001121 .
}

dgn-np:NP1267486.RAEQoCW2J56rqm3Ykv_RGlPNcpWfQjOkFugeG1AapqRBk130_provenance {
  dgn-np:NP1267486.RAEQoCW2J56rqm3Ykv_RGlPNcpWfQjOkFugeG1AapqRBk130_assertion dcterms:description
      "[Similar to its existing use in the diagnosis of monogenic dyslipidemias such as familial hypercholesterolemia, clinical inquiry regarding family history was identified as an important determinant of eligibility for APOE genotyping performed in the context of chronic disease risk management.]. 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:25731628;
    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:NP1267486.RAEQoCW2J56rqm3Ykv_RGlPNcpWfQjOkFugeG1AapqRBk130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:20+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" .
}