@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP53426.RAcOmv4A_rq7pK8KBnl9TTCqLPRiB_-FP2LeSm_fGgvFI> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP53426.RAcOmv4A_rq7pK8KBnl9TTCqLPRiB_-FP2LeSm_fGgvFI130_head {
  this: np:hasAssertion dgn-np:NP53426.RAcOmv4A_rq7pK8KBnl9TTCqLPRiB_-FP2LeSm_fGgvFI130_assertion;
    np:hasProvenance dgn-np:NP53426.RAcOmv4A_rq7pK8KBnl9TTCqLPRiB_-FP2LeSm_fGgvFI130_provenance;
    np:hasPublicationInfo dgn-np:NP53426.RAcOmv4A_rq7pK8KBnl9TTCqLPRiB_-FP2LeSm_fGgvFI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP53426.RAcOmv4A_rq7pK8KBnl9TTCqLPRiB_-FP2LeSm_fGgvFI130_assertion a np:Assertion .
  
  dgn-np:NP53426.RAcOmv4A_rq7pK8KBnl9TTCqLPRiB_-FP2LeSm_fGgvFI130_provenance a np:Provenance .
  
  dgn-np:NP53426.RAcOmv4A_rq7pK8KBnl9TTCqLPRiB_-FP2LeSm_fGgvFI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP53426.RAcOmv4A_rq7pK8KBnl9TTCqLPRiB_-FP2LeSm_fGgvFI130_assertion {
  miriam-gene:2099 a ncit:C16612 .
  
  lld:C0149931 a ncit:C7057 .
  
  dgn-gda:DGN0f11d4f42de57c4bb6297fb5fa49cca2 sio:SIO_000628 miriam-gene:2099, lld:C0149931;
    a sio:SIO_001122 .
}

dgn-np:NP53426.RAcOmv4A_rq7pK8KBnl9TTCqLPRiB_-FP2LeSm_fGgvFI130_provenance {
  dgn-np:NP53426.RAcOmv4A_rq7pK8KBnl9TTCqLPRiB_-FP2LeSm_fGgvFI130_assertion dcterms:description
      "[Interaction analysis of the PROGINS variant with our previously reported associated ESR1 594A variant showed that individuals who possessed at least one copy of both risk alleles were 3.2 times more likely to suffer migraine.]. 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:15654614;
    prov:wasDerivedFrom dgn-void:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP53426.RAcOmv4A_rq7pK8KBnl9TTCqLPRiB_-FP2LeSm_fGgvFI130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:09+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}