@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP655837.RAlzRYIAs3DkEc5AO9-AKddD7VdFpx-e2yajPJ-7PZywU> .
@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:NP655837.RAlzRYIAs3DkEc5AO9-AKddD7VdFpx-e2yajPJ-7PZywU130_head {
  this: np:hasAssertion dgn-np:NP655837.RAlzRYIAs3DkEc5AO9-AKddD7VdFpx-e2yajPJ-7PZywU130_assertion;
    np:hasProvenance dgn-np:NP655837.RAlzRYIAs3DkEc5AO9-AKddD7VdFpx-e2yajPJ-7PZywU130_provenance;
    np:hasPublicationInfo dgn-np:NP655837.RAlzRYIAs3DkEc5AO9-AKddD7VdFpx-e2yajPJ-7PZywU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP655837.RAlzRYIAs3DkEc5AO9-AKddD7VdFpx-e2yajPJ-7PZywU130_assertion a np:Assertion .
  
  dgn-np:NP655837.RAlzRYIAs3DkEc5AO9-AKddD7VdFpx-e2yajPJ-7PZywU130_provenance a np:Provenance .
  
  dgn-np:NP655837.RAlzRYIAs3DkEc5AO9-AKddD7VdFpx-e2yajPJ-7PZywU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP655837.RAlzRYIAs3DkEc5AO9-AKddD7VdFpx-e2yajPJ-7PZywU130_assertion {
  miriam-gene:7450 a ncit:C16612 .
  
  lld:C0010068 a ncit:C7057 .
  
  dgn-gda:DGN3b0dcda812ad784d0c1f0cf922ddfff2 sio:SIO_000628 miriam-gene:7450, lld:C0010068;
    a sio:SIO_001121 .
}

dgn-np:NP655837.RAlzRYIAs3DkEc5AO9-AKddD7VdFpx-e2yajPJ-7PZywU130_provenance {
  dgn-np:NP655837.RAlzRYIAs3DkEc5AO9-AKddD7VdFpx-e2yajPJ-7PZywU130_assertion dcterms:description
      "[In summary, vWF gene polymorphisms at site A1381T were not associated with coronary heart disease, but plasma vWF levels were influenced by vWF gene polymorphisms at site A1381T, blood type and coronary heart disease.]. 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:22923007;
    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:NP655837.RAlzRYIAs3DkEc5AO9-AKddD7VdFpx-e2yajPJ-7PZywU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:35+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" .
}