@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP727293.RAfK4C_oseTcsrtAxwXmj3EBoY8V6PyqyM-oygXzbjj0U> .
@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:NP727293.RAfK4C_oseTcsrtAxwXmj3EBoY8V6PyqyM-oygXzbjj0U130_head {
  this: np:hasAssertion dgn-np:NP727293.RAfK4C_oseTcsrtAxwXmj3EBoY8V6PyqyM-oygXzbjj0U130_assertion;
    np:hasProvenance dgn-np:NP727293.RAfK4C_oseTcsrtAxwXmj3EBoY8V6PyqyM-oygXzbjj0U130_provenance;
    np:hasPublicationInfo dgn-np:NP727293.RAfK4C_oseTcsrtAxwXmj3EBoY8V6PyqyM-oygXzbjj0U130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP727293.RAfK4C_oseTcsrtAxwXmj3EBoY8V6PyqyM-oygXzbjj0U130_assertion a np:Assertion .
  
  dgn-np:NP727293.RAfK4C_oseTcsrtAxwXmj3EBoY8V6PyqyM-oygXzbjj0U130_provenance a np:Provenance .
  
  dgn-np:NP727293.RAfK4C_oseTcsrtAxwXmj3EBoY8V6PyqyM-oygXzbjj0U130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP727293.RAfK4C_oseTcsrtAxwXmj3EBoY8V6PyqyM-oygXzbjj0U130_assertion {
  miriam-gene:221477 a ncit:C16612 .
  
  lld:C2733225 a ncit:C7057 .
  
  dgn-gda:DGN2750d434f9452084eaf996ba25741632 sio:SIO_000628 miriam-gene:221477, lld:C2733225;
    a sio:SIO_001121 .
}

dgn-np:NP727293.RAfK4C_oseTcsrtAxwXmj3EBoY8V6PyqyM-oygXzbjj0U130_provenance {
  dgn-np:NP727293.RAfK4C_oseTcsrtAxwXmj3EBoY8V6PyqyM-oygXzbjj0U130_assertion dcterms:description
      "[The single nucleotide polymorphism (SNP) rs11066001 of BRAP has been shown to be associated with myocardial infarction (MI), coronary atherosclerosis and carotid atherosclerosis, but it is not clear whether it also plays a role in peripheral artery disease (PAD).]. 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:21301165;
    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:NP727293.RAfK4C_oseTcsrtAxwXmj3EBoY8V6PyqyM-oygXzbjj0U130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:21+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" .
}