@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP315114.RAhkHjm94ANl4OMCkCfQtDa0KNKWGDqmVCJEbMHufoH5M> .
@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:NP315114.RAhkHjm94ANl4OMCkCfQtDa0KNKWGDqmVCJEbMHufoH5M130_head {
  this: np:hasAssertion dgn-np:NP315114.RAhkHjm94ANl4OMCkCfQtDa0KNKWGDqmVCJEbMHufoH5M130_assertion;
    np:hasProvenance dgn-np:NP315114.RAhkHjm94ANl4OMCkCfQtDa0KNKWGDqmVCJEbMHufoH5M130_provenance;
    np:hasPublicationInfo dgn-np:NP315114.RAhkHjm94ANl4OMCkCfQtDa0KNKWGDqmVCJEbMHufoH5M130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP315114.RAhkHjm94ANl4OMCkCfQtDa0KNKWGDqmVCJEbMHufoH5M130_assertion a np:Assertion .
  
  dgn-np:NP315114.RAhkHjm94ANl4OMCkCfQtDa0KNKWGDqmVCJEbMHufoH5M130_provenance a np:Provenance .
  
  dgn-np:NP315114.RAhkHjm94ANl4OMCkCfQtDa0KNKWGDqmVCJEbMHufoH5M130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP315114.RAhkHjm94ANl4OMCkCfQtDa0KNKWGDqmVCJEbMHufoH5M130_assertion {
  miriam-gene:5444 a ncit:C16612 .
  
  lld:C0149931 a ncit:C7057 .
  
  dgn-gda:DGNb0dd60ad2234e93fe2bb3d27fc6a692b sio:SIO_000628 miriam-gene:5444, lld:C0149931;
    a sio:SIO_001121 .
}

dgn-np:NP315114.RAhkHjm94ANl4OMCkCfQtDa0KNKWGDqmVCJEbMHufoH5M130_provenance {
  dgn-np:NP315114.RAhkHjm94ANl4OMCkCfQtDa0KNKWGDqmVCJEbMHufoH5M130_assertion dcterms:description
      "[The frequencies of the PON1 genotypes and PON1 allelic variants did not differ significantly between patients with migraine and controls, and were unrelated with gender, family history of migraine, and presence or absence of aura.]. 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:20407783;
    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:NP315114.RAhkHjm94ANl4OMCkCfQtDa0KNKWGDqmVCJEbMHufoH5M130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:00+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" .
}