@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP299227.RA_dD5aL_KTk0gw78cibGJpWR7ZKj8EpdZqPQYtW-tbkc> .
@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:NP299227.RA_dD5aL_KTk0gw78cibGJpWR7ZKj8EpdZqPQYtW-tbkc130_head {
  this: np:hasAssertion dgn-np:NP299227.RA_dD5aL_KTk0gw78cibGJpWR7ZKj8EpdZqPQYtW-tbkc130_assertion;
    np:hasProvenance dgn-np:NP299227.RA_dD5aL_KTk0gw78cibGJpWR7ZKj8EpdZqPQYtW-tbkc130_provenance;
    np:hasPublicationInfo dgn-np:NP299227.RA_dD5aL_KTk0gw78cibGJpWR7ZKj8EpdZqPQYtW-tbkc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP299227.RA_dD5aL_KTk0gw78cibGJpWR7ZKj8EpdZqPQYtW-tbkc130_assertion a np:Assertion .
  
  dgn-np:NP299227.RA_dD5aL_KTk0gw78cibGJpWR7ZKj8EpdZqPQYtW-tbkc130_provenance a np:Provenance .
  
  dgn-np:NP299227.RA_dD5aL_KTk0gw78cibGJpWR7ZKj8EpdZqPQYtW-tbkc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP299227.RA_dD5aL_KTk0gw78cibGJpWR7ZKj8EpdZqPQYtW-tbkc130_assertion {
  miriam-gene:338 a ncit:C16612 .
  
  lld:C0010054 a ncit:C7057 .
  
  dgn-gda:DGNef589a78beca7776470f303e42d89263 sio:SIO_000628 miriam-gene:338, lld:C0010054;
    a sio:SIO_001121 .
}

dgn-np:NP299227.RA_dD5aL_KTk0gw78cibGJpWR7ZKj8EpdZqPQYtW-tbkc130_provenance {
  dgn-np:NP299227.RA_dD5aL_KTk0gw78cibGJpWR7ZKj8EpdZqPQYtW-tbkc130_assertion dcterms:description
      "[The role of genetic variation at the 3' end of the apolipoprotein B gene locus in the development of coronary heart disease and the regulation of the serum levels of various lipoproteins was studied by using two common restriction fragment length polymorphisms detected with the enzymes Xba I and EcoR I.]. 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:1967524;
    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:NP299227.RA_dD5aL_KTk0gw78cibGJpWR7ZKj8EpdZqPQYtW-tbkc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:50+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" .
}