@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP216241.RAhS2mocn9OdRjS3ifU78hHSeDoCfrJeYzf7eeH-CwLFI> .
@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:NP216241.RAhS2mocn9OdRjS3ifU78hHSeDoCfrJeYzf7eeH-CwLFI130_head {
  this: np:hasAssertion dgn-np:NP216241.RAhS2mocn9OdRjS3ifU78hHSeDoCfrJeYzf7eeH-CwLFI130_assertion ;
    np:hasProvenance dgn-np:NP216241.RAhS2mocn9OdRjS3ifU78hHSeDoCfrJeYzf7eeH-CwLFI130_provenance ;
    np:hasPublicationInfo dgn-np:NP216241.RAhS2mocn9OdRjS3ifU78hHSeDoCfrJeYzf7eeH-CwLFI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP216241.RAhS2mocn9OdRjS3ifU78hHSeDoCfrJeYzf7eeH-CwLFI130_assertion a np:Assertion .
  dgn-np:NP216241.RAhS2mocn9OdRjS3ifU78hHSeDoCfrJeYzf7eeH-CwLFI130_provenance a np:Provenance .
  dgn-np:NP216241.RAhS2mocn9OdRjS3ifU78hHSeDoCfrJeYzf7eeH-CwLFI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP216241.RAhS2mocn9OdRjS3ifU78hHSeDoCfrJeYzf7eeH-CwLFI130_assertion {
  miriam-gene:2099 a ncit:C16612 .
  lld:C0149931 a ncit:C7057 .
  dgn-gda:DGN8b02b4a7f624c7390083eed3e91da55e sio:SIO_000628 miriam-gene:2099 , lld:C0149931 ;
    a sio:SIO_001121 .
}
dgn-np:NP216241.RAhS2mocn9OdRjS3ifU78hHSeDoCfrJeYzf7eeH-CwLFI130_provenance {
  dgn-np:NP216241.RAhS2mocn9OdRjS3ifU78hHSeDoCfrJeYzf7eeH-CwLFI130_assertion dcterms:description "[In a case-control study, including 210 Caucasoid migraine patients and 210 controls, we examined association between three single nucleotide polymorphisms in the coding region of ESR1, rs2077642, rs1801132, and rs2228480, and an Alu insertion in PGR, and migraine, migraine without aura or migraine with 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:19175383 ;
    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:NP216241.RAhS2mocn9OdRjS3ifU78hHSeDoCfrJeYzf7eeH-CwLFI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:00+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" .
}