@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP337156.RAJV4dJSrbH0JTOFag1jOr8WDzK_EQ1hGCVcl2eHzzmBs> .
@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:NP337156.RAJV4dJSrbH0JTOFag1jOr8WDzK_EQ1hGCVcl2eHzzmBs130_head {
  this: np:hasAssertion dgn-np:NP337156.RAJV4dJSrbH0JTOFag1jOr8WDzK_EQ1hGCVcl2eHzzmBs130_assertion;
    np:hasProvenance dgn-np:NP337156.RAJV4dJSrbH0JTOFag1jOr8WDzK_EQ1hGCVcl2eHzzmBs130_provenance;
    np:hasPublicationInfo dgn-np:NP337156.RAJV4dJSrbH0JTOFag1jOr8WDzK_EQ1hGCVcl2eHzzmBs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP337156.RAJV4dJSrbH0JTOFag1jOr8WDzK_EQ1hGCVcl2eHzzmBs130_assertion a np:Assertion .
  
  dgn-np:NP337156.RAJV4dJSrbH0JTOFag1jOr8WDzK_EQ1hGCVcl2eHzzmBs130_provenance a np:Provenance .
  
  dgn-np:NP337156.RAJV4dJSrbH0JTOFag1jOr8WDzK_EQ1hGCVcl2eHzzmBs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP337156.RAJV4dJSrbH0JTOFag1jOr8WDzK_EQ1hGCVcl2eHzzmBs130_assertion {
  miriam-gene:668 a ncit:C16612 .
  
  lld:C0000768 a ncit:C7057 .
  
  dgn-gda:DGN5134769d4ebacb8274873d0c2e940799 sio:SIO_000628 miriam-gene:668, lld:C0000768;
    a sio:SIO_001121 .
}

dgn-np:NP337156.RAJV4dJSrbH0JTOFag1jOr8WDzK_EQ1hGCVcl2eHzzmBs130_provenance {
  dgn-np:NP337156.RAJV4dJSrbH0JTOFag1jOr8WDzK_EQ1hGCVcl2eHzzmBs130_assertion dcterms:description
      "[Blepharophimosis-ptosis-epicanthus inversus syndrome (BPES), an autosomal dominant syndrome in which an eyelid malformation is associated (type I) or not (type II) with premature ovarian failure (POF), has recently been ascribed to mutations in the forkhead transcription factor 2 (FOXL2) gene.]. 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:15450400;
    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:NP337156.RAJV4dJSrbH0JTOFag1jOr8WDzK_EQ1hGCVcl2eHzzmBs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:18+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" .
}