@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP93947.RAe91rGubzbg8c08_d1VJQ1ZZ9rhaCKOM7Hsxgr9ZfK4c> .
@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:NP93947.RAe91rGubzbg8c08_d1VJQ1ZZ9rhaCKOM7Hsxgr9ZfK4c130_head {
  this: np:hasAssertion dgn-np:NP93947.RAe91rGubzbg8c08_d1VJQ1ZZ9rhaCKOM7Hsxgr9ZfK4c130_assertion;
    np:hasProvenance dgn-np:NP93947.RAe91rGubzbg8c08_d1VJQ1ZZ9rhaCKOM7Hsxgr9ZfK4c130_provenance;
    np:hasPublicationInfo dgn-np:NP93947.RAe91rGubzbg8c08_d1VJQ1ZZ9rhaCKOM7Hsxgr9ZfK4c130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP93947.RAe91rGubzbg8c08_d1VJQ1ZZ9rhaCKOM7Hsxgr9ZfK4c130_assertion a np:Assertion .
  
  dgn-np:NP93947.RAe91rGubzbg8c08_d1VJQ1ZZ9rhaCKOM7Hsxgr9ZfK4c130_provenance a np:Provenance .
  
  dgn-np:NP93947.RAe91rGubzbg8c08_d1VJQ1ZZ9rhaCKOM7Hsxgr9ZfK4c130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP93947.RAe91rGubzbg8c08_d1VJQ1ZZ9rhaCKOM7Hsxgr9ZfK4c130_assertion {
  miriam-gene:337880 a ncit:C16612 .
  
  lld:C0007273 a ncit:C7057 .
  
  dgn-gda:DGN030361656f9642e0c7492716c449c508 sio:SIO_000628 miriam-gene:337880, lld:C0007273;
    a sio:SIO_001122 .
}

dgn-np:NP93947.RAe91rGubzbg8c08_d1VJQ1ZZ9rhaCKOM7Hsxgr9ZfK4c130_provenance {
  dgn-np:NP93947.RAe91rGubzbg8c08_d1VJQ1ZZ9rhaCKOM7Hsxgr9ZfK4c130_assertion dcterms:description
      "[The results from this GWAS generate hypotheses regarding several SNPs that may be associated with SCA phenotypes in multiple arterial beds. Given the number of tests conducted, subsequent independent replication in a staged approach is essential to identify genetic variants that may be implicated in atherosclerosis.]. 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:17903303;
    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:NP93947.RAe91rGubzbg8c08_d1VJQ1ZZ9rhaCKOM7Hsxgr9ZfK4c130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:46+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" .
}