@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP77676.RADbTgg8WEhvydlpSyAM7Lx_G2TD70HeqS_iGKNRhZAu8> .
@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:NP77676.RADbTgg8WEhvydlpSyAM7Lx_G2TD70HeqS_iGKNRhZAu8130_head {
  this: np:hasAssertion dgn-np:NP77676.RADbTgg8WEhvydlpSyAM7Lx_G2TD70HeqS_iGKNRhZAu8130_assertion;
    np:hasProvenance dgn-np:NP77676.RADbTgg8WEhvydlpSyAM7Lx_G2TD70HeqS_iGKNRhZAu8130_provenance;
    np:hasPublicationInfo dgn-np:NP77676.RADbTgg8WEhvydlpSyAM7Lx_G2TD70HeqS_iGKNRhZAu8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP77676.RADbTgg8WEhvydlpSyAM7Lx_G2TD70HeqS_iGKNRhZAu8130_assertion a np:Assertion .
  
  dgn-np:NP77676.RADbTgg8WEhvydlpSyAM7Lx_G2TD70HeqS_iGKNRhZAu8130_provenance a np:Provenance .
  
  dgn-np:NP77676.RADbTgg8WEhvydlpSyAM7Lx_G2TD70HeqS_iGKNRhZAu8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP77676.RADbTgg8WEhvydlpSyAM7Lx_G2TD70HeqS_iGKNRhZAu8130_assertion {
  miriam-gene:11117 a ncit:C16612 .
  
  lld:C0020538 a ncit:C7057 .
  
  dgn-gda:DGNa3fcffa9181c26f7f37092baa63f4a08 sio:SIO_000628 miriam-gene:11117, lld:C0020538;
    a sio:SIO_001122 .
}

dgn-np:NP77676.RADbTgg8WEhvydlpSyAM7Lx_G2TD70HeqS_iGKNRhZAu8130_provenance {
  dgn-np:NP77676.RADbTgg8WEhvydlpSyAM7Lx_G2TD70HeqS_iGKNRhZAu8130_assertion dcterms:description
      "[We confirmed that rs2289360, rs2011616, and rs2304682 in the human EMILIN1 gene, as well as the haplotype constructed using rs2536512, rs2011616, and rs17881426 are useful genetic markers of EH in Japanese men.]. 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:20186130;
    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:NP77676.RADbTgg8WEhvydlpSyAM7Lx_G2TD70HeqS_iGKNRhZAu8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:38+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" .
}