@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP169514.RAUceE7YWukPoXUtZr575jscmHm12Wx0fN413nxKfsEB4> .
@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:NP169514.RAUceE7YWukPoXUtZr575jscmHm12Wx0fN413nxKfsEB4130_head {
  this: np:hasAssertion dgn-np:NP169514.RAUceE7YWukPoXUtZr575jscmHm12Wx0fN413nxKfsEB4130_assertion;
    np:hasProvenance dgn-np:NP169514.RAUceE7YWukPoXUtZr575jscmHm12Wx0fN413nxKfsEB4130_provenance;
    np:hasPublicationInfo dgn-np:NP169514.RAUceE7YWukPoXUtZr575jscmHm12Wx0fN413nxKfsEB4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP169514.RAUceE7YWukPoXUtZr575jscmHm12Wx0fN413nxKfsEB4130_assertion a np:Assertion .
  
  dgn-np:NP169514.RAUceE7YWukPoXUtZr575jscmHm12Wx0fN413nxKfsEB4130_provenance a np:Provenance .
  
  dgn-np:NP169514.RAUceE7YWukPoXUtZr575jscmHm12Wx0fN413nxKfsEB4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP169514.RAUceE7YWukPoXUtZr575jscmHm12Wx0fN413nxKfsEB4130_assertion {
  miriam-gene:64241 a ncit:C16612 .
  
  lld:C0010068 a ncit:C7057 .
  
  dgn-gda:DGN2d87f01db0e31eb9103b1d865c86467d sio:SIO_000628 miriam-gene:64241, lld:C0010068;
    a sio:SIO_001121 .
}

dgn-np:NP169514.RAUceE7YWukPoXUtZr575jscmHm12Wx0fN413nxKfsEB4130_provenance {
  dgn-np:NP169514.RAUceE7YWukPoXUtZr575jscmHm12Wx0fN413nxKfsEB4130_assertion dcterms:description
      "[Determinations of allele frequencies of four common ABCG8 polymorphisms (D19H, Y54C, T400K, and A632V) were carried out in 241 unrelated patients with ischemic stroke, 148 patients with coronary heart disease, and 191 blood donors (controls).]. 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:20854103;
    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:NP169514.RAUceE7YWukPoXUtZr575jscmHm12Wx0fN413nxKfsEB4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:31+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" .
}