@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP197171.RAiIyDQXKXdi_4i3d-He1YMMJ-GVGTBHZOPbSQXR6TM5o> .
@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:NP197171.RAiIyDQXKXdi_4i3d-He1YMMJ-GVGTBHZOPbSQXR6TM5o130_head {
  this: np:hasAssertion dgn-np:NP197171.RAiIyDQXKXdi_4i3d-He1YMMJ-GVGTBHZOPbSQXR6TM5o130_assertion ;
    np:hasProvenance dgn-np:NP197171.RAiIyDQXKXdi_4i3d-He1YMMJ-GVGTBHZOPbSQXR6TM5o130_provenance ;
    np:hasPublicationInfo dgn-np:NP197171.RAiIyDQXKXdi_4i3d-He1YMMJ-GVGTBHZOPbSQXR6TM5o130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP197171.RAiIyDQXKXdi_4i3d-He1YMMJ-GVGTBHZOPbSQXR6TM5o130_assertion a np:Assertion .
  dgn-np:NP197171.RAiIyDQXKXdi_4i3d-He1YMMJ-GVGTBHZOPbSQXR6TM5o130_provenance a np:Provenance .
  dgn-np:NP197171.RAiIyDQXKXdi_4i3d-He1YMMJ-GVGTBHZOPbSQXR6TM5o130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP197171.RAiIyDQXKXdi_4i3d-He1YMMJ-GVGTBHZOPbSQXR6TM5o130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  lld:C0154723 a ncit:C7057 .
  dgn-gda:DGNb32395c8e26874d7750870d73200b49b sio:SIO_000628 miriam-gene:4524 , lld:C0154723 ;
    a sio:SIO_001121 .
}
dgn-np:NP197171.RAiIyDQXKXdi_4i3d-He1YMMJ-GVGTBHZOPbSQXR6TM5o130_provenance {
  dgn-np:NP197171.RAiIyDQXKXdi_4i3d-He1YMMJ-GVGTBHZOPbSQXR6TM5o130_assertion dcterms:description "[A first genotype-migraine association study was conducted on 100 patients with migraine with aura (MA), 106 with migraine without aura (MO), and 105 subjects without migraine, which provided evidence in favor of association of the TT677 MTHFR genotype with increased risk of MA compared with both control subjects (OR, 2.48; 95% CI, 1.11 to 5.58) and patients with MO (OR, 2.21; 95% CI, 1.01 to 4.82).]. 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:17962595 ;
    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:NP197171.RAiIyDQXKXdi_4i3d-He1YMMJ-GVGTBHZOPbSQXR6TM5o130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:48+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" .
}