@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP475431.RADoy-LNrwQsz8TbqG-63zPsR6XTX7ZbCIkOPvn1xSnCI> .
@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:NP475431.RADoy-LNrwQsz8TbqG-63zPsR6XTX7ZbCIkOPvn1xSnCI130_head {
  this: np:hasAssertion dgn-np:NP475431.RADoy-LNrwQsz8TbqG-63zPsR6XTX7ZbCIkOPvn1xSnCI130_assertion;
    np:hasProvenance dgn-np:NP475431.RADoy-LNrwQsz8TbqG-63zPsR6XTX7ZbCIkOPvn1xSnCI130_provenance;
    np:hasPublicationInfo dgn-np:NP475431.RADoy-LNrwQsz8TbqG-63zPsR6XTX7ZbCIkOPvn1xSnCI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP475431.RADoy-LNrwQsz8TbqG-63zPsR6XTX7ZbCIkOPvn1xSnCI130_assertion a np:Assertion .
  
  dgn-np:NP475431.RADoy-LNrwQsz8TbqG-63zPsR6XTX7ZbCIkOPvn1xSnCI130_provenance a np:Provenance .
  
  dgn-np:NP475431.RADoy-LNrwQsz8TbqG-63zPsR6XTX7ZbCIkOPvn1xSnCI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP475431.RADoy-LNrwQsz8TbqG-63zPsR6XTX7ZbCIkOPvn1xSnCI130_assertion {
  miriam-gene:4018 a ncit:C16612 .
  
  lld:C0151744 a ncit:C7057 .
  
  dgn-gda:DGN525974e23fd17f7b9606d14d9d5d2e7a sio:SIO_000628 miriam-gene:4018, lld:C0151744;
    a sio:SIO_001121 .
}

dgn-np:NP475431.RADoy-LNrwQsz8TbqG-63zPsR6XTX7ZbCIkOPvn1xSnCI130_provenance {
  dgn-np:NP475431.RADoy-LNrwQsz8TbqG-63zPsR6XTX7ZbCIkOPvn1xSnCI130_assertion dcterms:description
      "[Levels of lipoprotein(a) are primarily determined by variation in the LPA gene coding for the apolipoprotein(a) moiety of lipoprotein(a), and genetic epidemiologic studies have documented association of LPA copy number variants, influencing levels of lipoprotein(a), with risk of IHD.]. 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:20106478;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP475431.RADoy-LNrwQsz8TbqG-63zPsR6XTX7ZbCIkOPvn1xSnCI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:45+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" .
}