@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP93993.RAUKQFUtP4vxMca2X_J2G0UGHWXyP35gJU6WP82UyIkvs> .
@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:NP93993.RAUKQFUtP4vxMca2X_J2G0UGHWXyP35gJU6WP82UyIkvs130_head {
  this: np:hasAssertion dgn-np:NP93993.RAUKQFUtP4vxMca2X_J2G0UGHWXyP35gJU6WP82UyIkvs130_assertion;
    np:hasProvenance dgn-np:NP93993.RAUKQFUtP4vxMca2X_J2G0UGHWXyP35gJU6WP82UyIkvs130_provenance;
    np:hasPublicationInfo dgn-np:NP93993.RAUKQFUtP4vxMca2X_J2G0UGHWXyP35gJU6WP82UyIkvs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP93993.RAUKQFUtP4vxMca2X_J2G0UGHWXyP35gJU6WP82UyIkvs130_assertion a np:Assertion .
  
  dgn-np:NP93993.RAUKQFUtP4vxMca2X_J2G0UGHWXyP35gJU6WP82UyIkvs130_provenance a np:Provenance .
  
  dgn-np:NP93993.RAUKQFUtP4vxMca2X_J2G0UGHWXyP35gJU6WP82UyIkvs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP93993.RAUKQFUtP4vxMca2X_J2G0UGHWXyP35gJU6WP82UyIkvs130_assertion {
  miriam-gene:9882 a ncit:C16612 .
  
  lld:C0007282 a ncit:C7057 .
  
  dgn-gda:DGN047d45053b08a9c06474eb375be8b0a5 sio:SIO_000628 miriam-gene:9882, lld:C0007282;
    a sio:SIO_001122 .
}

dgn-np:NP93993.RAUKQFUtP4vxMca2X_J2G0UGHWXyP35gJU6WP82UyIkvs130_provenance {
  dgn-np:NP93993.RAUKQFUtP4vxMca2X_J2G0UGHWXyP35gJU6WP82UyIkvs130_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:NP93993.RAUKQFUtP4vxMca2X_J2G0UGHWXyP35gJU6WP82UyIkvs130_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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}