@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP55289.RA3crmTSZEcTggPiORPbAnMs1au1zC688BvKCYDUE8SuY> .
@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:NP55289.RA3crmTSZEcTggPiORPbAnMs1au1zC688BvKCYDUE8SuY130_head {
  this: np:hasAssertion dgn-np:NP55289.RA3crmTSZEcTggPiORPbAnMs1au1zC688BvKCYDUE8SuY130_assertion;
    np:hasProvenance dgn-np:NP55289.RA3crmTSZEcTggPiORPbAnMs1au1zC688BvKCYDUE8SuY130_provenance;
    np:hasPublicationInfo dgn-np:NP55289.RA3crmTSZEcTggPiORPbAnMs1au1zC688BvKCYDUE8SuY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP55289.RA3crmTSZEcTggPiORPbAnMs1au1zC688BvKCYDUE8SuY130_assertion a np:Assertion .
  
  dgn-np:NP55289.RA3crmTSZEcTggPiORPbAnMs1au1zC688BvKCYDUE8SuY130_provenance a np:Provenance .
  
  dgn-np:NP55289.RA3crmTSZEcTggPiORPbAnMs1au1zC688BvKCYDUE8SuY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP55289.RA3crmTSZEcTggPiORPbAnMs1au1zC688BvKCYDUE8SuY130_assertion {
  miriam-gene:4018 a ncit:C16612 .
  
  lld:C0027051 a ncit:C7057 .
  
  dgn-gda:DGNcbce7c01f33654c8525064b11a4dae87 sio:SIO_000628 miriam-gene:4018, lld:C0027051;
    a sio:SIO_001122 .
}

dgn-np:NP55289.RA3crmTSZEcTggPiORPbAnMs1au1zC688BvKCYDUE8SuY130_provenance {
  dgn-np:NP55289.RA3crmTSZEcTggPiORPbAnMs1au1zC688BvKCYDUE8SuY130_assertion dcterms:description
      "[ The K4 and PN repeat polymorphisms largely explain the high variability of serum Lp(a) levels. A haplotype with <or=8 PN and <or=22 K4 repeats is characterized by high concentrations of small Lp(a) particles. Our observation that this haplotype was associated with MI independently of Lp(a) serum levels may suggest that Lp(a) particle size in addition to its concentration may modulate MI risk in women.]. 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:12578871;
    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:NP55289.RA3crmTSZEcTggPiORPbAnMs1au1zC688BvKCYDUE8SuY130_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" .
}