@prefix dc: <http://purl.org/dc/terms/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP96303.RAUYp96I1TvEQbe9W9rv1zWNnIs_hH5_NVUJeSiBnM86Q> .
@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 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:NP96303.RAUYp96I1TvEQbe9W9rv1zWNnIs_hH5_NVUJeSiBnM86Q130_head {
  this: np:hasAssertion dgn-np:NP96303.RAUYp96I1TvEQbe9W9rv1zWNnIs_hH5_NVUJeSiBnM86Q130_assertion;
    np:hasProvenance dgn-np:NP96303.RAUYp96I1TvEQbe9W9rv1zWNnIs_hH5_NVUJeSiBnM86Q130_provenance;
    np:hasPublicationInfo dgn-np:NP96303.RAUYp96I1TvEQbe9W9rv1zWNnIs_hH5_NVUJeSiBnM86Q130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP96303.RAUYp96I1TvEQbe9W9rv1zWNnIs_hH5_NVUJeSiBnM86Q130_assertion a np:Assertion .
  
  dgn-np:NP96303.RAUYp96I1TvEQbe9W9rv1zWNnIs_hH5_NVUJeSiBnM86Q130_provenance a np:Provenance .
  
  dgn-np:NP96303.RAUYp96I1TvEQbe9W9rv1zWNnIs_hH5_NVUJeSiBnM86Q130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP96303.RAUYp96I1TvEQbe9W9rv1zWNnIs_hH5_NVUJeSiBnM86Q130_assertion {
  miriam-gene:100192386 a ncit:C16612 .
  
  lld:C0007222 a ncit:C7057 .
  
  dgn-gda:DGN4aff1ed3fd773c322e97265bc4537f08 sio:SIO_000628 miriam-gene:100192386,
      lld:C0007222;
    a sio:SIO_001122 .
}

dgn-np:NP96303.RAUYp96I1TvEQbe9W9rv1zWNnIs_hH5_NVUJeSiBnM86Q130_provenance {
  dgn-np:NP96303.RAUYp96I1TvEQbe9W9rv1zWNnIs_hH5_NVUJeSiBnM86Q130_assertion dc:description
      "[Our results provide some suggestion for an association of five SNPs with CVD events among women with migraine; none of the results was genome-wide significant. Four associations appeared among migraineurs with aura, two of those with ischemic stroke. Although our population is among the largest with migraine and incident CVD information, these results must be treated with caution, given the limited number of CVD events among women with migraine and the low minor allele frequencies for three of the SNPs. Our results await independent replication and should be considered hypothesis generating for future research.]. 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:21779381;
    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:NP96303.RAUYp96I1TvEQbe9W9rv1zWNnIs_hH5_NVUJeSiBnM86Q130_publicationInfo {
  this: dc:created "2014-10-02T12:32:48+02:00"^^xsd:dateTime;
    dc:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dc:rightsHolder dgn-void:IBIGroup;
    dc: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" .
}