@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP59579.RACbVFURxhnQNECEzOvFkFtUs9TS5aivAPa7R0cHRKaTE> .
@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:NP59579.RACbVFURxhnQNECEzOvFkFtUs9TS5aivAPa7R0cHRKaTE130_head {
  this: np:hasAssertion dgn-np:NP59579.RACbVFURxhnQNECEzOvFkFtUs9TS5aivAPa7R0cHRKaTE130_assertion;
    np:hasProvenance dgn-np:NP59579.RACbVFURxhnQNECEzOvFkFtUs9TS5aivAPa7R0cHRKaTE130_provenance;
    np:hasPublicationInfo dgn-np:NP59579.RACbVFURxhnQNECEzOvFkFtUs9TS5aivAPa7R0cHRKaTE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP59579.RACbVFURxhnQNECEzOvFkFtUs9TS5aivAPa7R0cHRKaTE130_assertion a np:Assertion .
  
  dgn-np:NP59579.RACbVFURxhnQNECEzOvFkFtUs9TS5aivAPa7R0cHRKaTE130_provenance a np:Provenance .
  
  dgn-np:NP59579.RACbVFURxhnQNECEzOvFkFtUs9TS5aivAPa7R0cHRKaTE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP59579.RACbVFURxhnQNECEzOvFkFtUs9TS5aivAPa7R0cHRKaTE130_assertion {
  miriam-gene:345 a ncit:C16612 .
  
  lld:C0010054 a ncit:C7057 .
  
  dgn-gda:DGN1ef39a1508d68f1e8469f90583c228b8 sio:SIO_000628 miriam-gene:345, lld:C0010054;
    a sio:SIO_001122 .
}

dgn-np:NP59579.RACbVFURxhnQNECEzOvFkFtUs9TS5aivAPa7R0cHRKaTE130_provenance {
  dgn-np:NP59579.RACbVFURxhnQNECEzOvFkFtUs9TS5aivAPa7R0cHRKaTE130_assertion dcterms:description
      "[ variation in LIPC (hepatic lipase) gene associates with clinical outcomes in Italian patients with established CAD. Further studies on the LIPC gene in CAD patients are warranted, in particular looking at the possible influences on clinical outcomes.]. 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:12964943;
    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:NP59579.RACbVFURxhnQNECEzOvFkFtUs9TS5aivAPa7R0cHRKaTE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:28+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" .
}