@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP55235.RArGQ2UVUXQosl8swz3dsDz_jfvPT8Ifig5Dspjt3NzTk> .
@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:NP55235.RArGQ2UVUXQosl8swz3dsDz_jfvPT8Ifig5Dspjt3NzTk130_head {
  this: np:hasAssertion dgn-np:NP55235.RArGQ2UVUXQosl8swz3dsDz_jfvPT8Ifig5Dspjt3NzTk130_assertion;
    np:hasProvenance dgn-np:NP55235.RArGQ2UVUXQosl8swz3dsDz_jfvPT8Ifig5Dspjt3NzTk130_provenance;
    np:hasPublicationInfo dgn-np:NP55235.RArGQ2UVUXQosl8swz3dsDz_jfvPT8Ifig5Dspjt3NzTk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP55235.RArGQ2UVUXQosl8swz3dsDz_jfvPT8Ifig5Dspjt3NzTk130_assertion a np:Assertion .
  
  dgn-np:NP55235.RArGQ2UVUXQosl8swz3dsDz_jfvPT8Ifig5Dspjt3NzTk130_provenance a np:Provenance .
  
  dgn-np:NP55235.RArGQ2UVUXQosl8swz3dsDz_jfvPT8Ifig5Dspjt3NzTk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP55235.RArGQ2UVUXQosl8swz3dsDz_jfvPT8Ifig5Dspjt3NzTk130_assertion {
  miriam-gene:4023 a ncit:C16612 .
  
  lld:C0002395 a ncit:C7057 .
  
  dgn-gda:DGNdb6cf9a900890d8aa40ccd2c52134165 sio:SIO_000628 miriam-gene:4023, lld:C0002395;
    a sio:SIO_001122 .
}

dgn-np:NP55235.RArGQ2UVUXQosl8swz3dsDz_jfvPT8Ifig5Dspjt3NzTk130_provenance {
  dgn-np:NP55235.RArGQ2UVUXQosl8swz3dsDz_jfvPT8Ifig5Dspjt3NzTk130_assertion dcterms:description
      "[These results indicate that a common polymorphism in the lipoprotein lipase gene modulates the risk level for sporadic AD in the eastern Canadian population but more importantly, indirectly modulates the pathophysiology of the brain in autopsy-confirmed cases.]. 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:16965549;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP55235.RArGQ2UVUXQosl8swz3dsDz_jfvPT8Ifig5Dspjt3NzTk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:25+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" .
}