@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP608660.RAVJ3bQKfxoL94rs9rN4E4jv4DK4HaqmXVh0hNIXbRt0w> .
@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:NP608660.RAVJ3bQKfxoL94rs9rN4E4jv4DK4HaqmXVh0hNIXbRt0w130_head {
  this: np:hasAssertion dgn-np:NP608660.RAVJ3bQKfxoL94rs9rN4E4jv4DK4HaqmXVh0hNIXbRt0w130_assertion;
    np:hasProvenance dgn-np:NP608660.RAVJ3bQKfxoL94rs9rN4E4jv4DK4HaqmXVh0hNIXbRt0w130_provenance;
    np:hasPublicationInfo dgn-np:NP608660.RAVJ3bQKfxoL94rs9rN4E4jv4DK4HaqmXVh0hNIXbRt0w130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP608660.RAVJ3bQKfxoL94rs9rN4E4jv4DK4HaqmXVh0hNIXbRt0w130_assertion a np:Assertion .
  
  dgn-np:NP608660.RAVJ3bQKfxoL94rs9rN4E4jv4DK4HaqmXVh0hNIXbRt0w130_provenance a np:Provenance .
  
  dgn-np:NP608660.RAVJ3bQKfxoL94rs9rN4E4jv4DK4HaqmXVh0hNIXbRt0w130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP608660.RAVJ3bQKfxoL94rs9rN4E4jv4DK4HaqmXVh0hNIXbRt0w130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  
  lld:C1402315 a ncit:C7057 .
  
  dgn-gda:DGN3210b9697f00d42277418153f9636bec sio:SIO_000628 miriam-gene:4524, lld:C1402315;
    a sio:SIO_001121 .
}

dgn-np:NP608660.RAVJ3bQKfxoL94rs9rN4E4jv4DK4HaqmXVh0hNIXbRt0w130_provenance {
  dgn-np:NP608660.RAVJ3bQKfxoL94rs9rN4E4jv4DK4HaqmXVh0hNIXbRt0w130_assertion dcterms:description
      "[The aim of our study was to evaluate the frequency of the C677T variant in the methylenetetrahydrofolate reductase (MTHFR) gene in patients with migraine with or without aura and to find an association between this variant and vascular lesions in magnetic resonance imaging of the head, presence of patent foramen ovale (PFO) and increased level of homocysteine.]. 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:23161188;
    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:NP608660.RAVJ3bQKfxoL94rs9rN4E4jv4DK4HaqmXVh0hNIXbRt0w130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:05+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" .
}