@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP48377.RAykgAAMGqpzC0N1dpBDjfduHzagcM6s6Qc1omuqRYK7g> .
@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:NP48377.RAykgAAMGqpzC0N1dpBDjfduHzagcM6s6Qc1omuqRYK7g130_head {
  this: np:hasAssertion dgn-np:NP48377.RAykgAAMGqpzC0N1dpBDjfduHzagcM6s6Qc1omuqRYK7g130_assertion;
    np:hasProvenance dgn-np:NP48377.RAykgAAMGqpzC0N1dpBDjfduHzagcM6s6Qc1omuqRYK7g130_provenance;
    np:hasPublicationInfo dgn-np:NP48377.RAykgAAMGqpzC0N1dpBDjfduHzagcM6s6Qc1omuqRYK7g130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP48377.RAykgAAMGqpzC0N1dpBDjfduHzagcM6s6Qc1omuqRYK7g130_assertion a np:Assertion .
  
  dgn-np:NP48377.RAykgAAMGqpzC0N1dpBDjfduHzagcM6s6Qc1omuqRYK7g130_provenance a np:Provenance .
  
  dgn-np:NP48377.RAykgAAMGqpzC0N1dpBDjfduHzagcM6s6Qc1omuqRYK7g130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP48377.RAykgAAMGqpzC0N1dpBDjfduHzagcM6s6Qc1omuqRYK7g130_assertion {
  miriam-gene:338 a ncit:C16612 .
  
  lld:C1956346 a ncit:C7057 .
  
  dgn-gda:DGN69bf7763f0ce86b3400e0a0bf58ac972 sio:SIO_000628 miriam-gene:338, lld:C1956346;
    a sio:SIO_001122 .
}

dgn-np:NP48377.RAykgAAMGqpzC0N1dpBDjfduHzagcM6s6Qc1omuqRYK7g130_provenance {
  dgn-np:NP48377.RAykgAAMGqpzC0N1dpBDjfduHzagcM6s6Qc1omuqRYK7g130_assertion dcterms:description
      "[The association of genetic markers at the apolipoprotein B gene (APOB) (XbaI, MspI, and EcoRI polymorphisms) and the lipoprotein lipase gene (LPL) (PvuII polymorphism) with coronary artery disease (CAD) and with variation in plasma lipid levels (total cholesterol, high-density lipoprotein cholesterol, and total triglycerides) was studied in 94 male patients with CAD diagnosed by angiography and in 122 unrelated men of Russian descent free of clinical signs of CAD.]. 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:9489234;
    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:NP48377.RAykgAAMGqpzC0N1dpBDjfduHzagcM6s6Qc1omuqRYK7g130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:22+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" .
}