@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP86740.RA_1wzJ0e-inLJ-_pevrb-APHaICOquUOFXlkkcTaX0K0> .
@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:NP86740.RA_1wzJ0e-inLJ-_pevrb-APHaICOquUOFXlkkcTaX0K0130_head {
  this: np:hasAssertion dgn-np:NP86740.RA_1wzJ0e-inLJ-_pevrb-APHaICOquUOFXlkkcTaX0K0130_assertion;
    np:hasProvenance dgn-np:NP86740.RA_1wzJ0e-inLJ-_pevrb-APHaICOquUOFXlkkcTaX0K0130_provenance;
    np:hasPublicationInfo dgn-np:NP86740.RA_1wzJ0e-inLJ-_pevrb-APHaICOquUOFXlkkcTaX0K0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP86740.RA_1wzJ0e-inLJ-_pevrb-APHaICOquUOFXlkkcTaX0K0130_assertion a np:Assertion .
  
  dgn-np:NP86740.RA_1wzJ0e-inLJ-_pevrb-APHaICOquUOFXlkkcTaX0K0130_provenance a np:Provenance .
  
  dgn-np:NP86740.RA_1wzJ0e-inLJ-_pevrb-APHaICOquUOFXlkkcTaX0K0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP86740.RA_1wzJ0e-inLJ-_pevrb-APHaICOquUOFXlkkcTaX0K0130_assertion {
  miriam-gene:3176 a ncit:C16612 .
  
  lld:C0149931 a ncit:C7057 .
  
  dgn-gda:DGNc48d9023bdefae47d58c3ea5d5490daa sio:SIO_000628 miriam-gene:3176, lld:C0149931;
    a sio:SIO_001122 .
}

dgn-np:NP86740.RA_1wzJ0e-inLJ-_pevrb-APHaICOquUOFXlkkcTaX0K0130_provenance {
  dgn-np:NP86740.RA_1wzJ0e-inLJ-_pevrb-APHaICOquUOFXlkkcTaX0K0130_assertion dcterms:description
      "[The frequencies of the HNMT genotypes and allelic variants did not differ significantly between migraine patients and controls, and were unrelated with the age of onset of migraine attacks, gender, personal history of allergic diseases, family history of migraine, or presence 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:18266724;
    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:NP86740.RA_1wzJ0e-inLJ-_pevrb-APHaICOquUOFXlkkcTaX0K0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:43+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" .
}