@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP55331.RA74yeSWrsD7pHj318JaBfeGFXIVWwvW_XEuLktGr5hNM> .
@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:NP55331.RA74yeSWrsD7pHj318JaBfeGFXIVWwvW_XEuLktGr5hNM130_head {
  this: np:hasAssertion dgn-np:NP55331.RA74yeSWrsD7pHj318JaBfeGFXIVWwvW_XEuLktGr5hNM130_assertion;
    np:hasProvenance dgn-np:NP55331.RA74yeSWrsD7pHj318JaBfeGFXIVWwvW_XEuLktGr5hNM130_provenance;
    np:hasPublicationInfo dgn-np:NP55331.RA74yeSWrsD7pHj318JaBfeGFXIVWwvW_XEuLktGr5hNM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP55331.RA74yeSWrsD7pHj318JaBfeGFXIVWwvW_XEuLktGr5hNM130_assertion a np:Assertion .
  
  dgn-np:NP55331.RA74yeSWrsD7pHj318JaBfeGFXIVWwvW_XEuLktGr5hNM130_provenance a np:Provenance .
  
  dgn-np:NP55331.RA74yeSWrsD7pHj318JaBfeGFXIVWwvW_XEuLktGr5hNM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP55331.RA74yeSWrsD7pHj318JaBfeGFXIVWwvW_XEuLktGr5hNM130_assertion {
  miriam-gene:3990 a ncit:C16612 .
  
  lld:C0028754 a ncit:C7057 .
  
  dgn-gda:DGNa93e6eec309bc04fe2645a339b813fba sio:SIO_000628 miriam-gene:3990, lld:C0028754;
    a sio:SIO_001122 .
}

dgn-np:NP55331.RA74yeSWrsD7pHj318JaBfeGFXIVWwvW_XEuLktGr5hNM130_provenance {
  dgn-np:NP55331.RA74yeSWrsD7pHj318JaBfeGFXIVWwvW_XEuLktGr5hNM130_assertion dcterms:description
      "[1) the LIPC promoter polymorphism contributes to variation in HLA and HDL(2) in the three ethnic groups; 2) WA men had higher HLA than BA and JA men, related to ethnic differences in central adiposity but not LIPC allele frequency; and 3) the higher HLA in WA men did not contribute to the ethnic differences in HDL, as the differences in HDL were made up entirely of differences in HDL(3) and not HDL(2).]. 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:14657196;
    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:NP55331.RA74yeSWrsD7pHj318JaBfeGFXIVWwvW_XEuLktGr5hNM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:26+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" .
}