@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP689659.RAm8v8st_M88pNpC7BL6XBBMlQcJIolEScBeDUJujaCmc> .
@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/v4.0.0/void/> .
dgn-np:NP689659.RAm8v8st_M88pNpC7BL6XBBMlQcJIolEScBeDUJujaCmc130_head {
   this: np:hasAssertion dgn-np:NP689659.RAm8v8st_M88pNpC7BL6XBBMlQcJIolEScBeDUJujaCmc130_assertion ;
    np:hasProvenance dgn-np:NP689659.RAm8v8st_M88pNpC7BL6XBBMlQcJIolEScBeDUJujaCmc130_provenance ;
    np:hasPublicationInfo dgn-np:NP689659.RAm8v8st_M88pNpC7BL6XBBMlQcJIolEScBeDUJujaCmc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP689659.RAm8v8st_M88pNpC7BL6XBBMlQcJIolEScBeDUJujaCmc130_assertion a np:Assertion .
  dgn-np:NP689659.RAm8v8st_M88pNpC7BL6XBBMlQcJIolEScBeDUJujaCmc130_provenance a np:Provenance .
  dgn-np:NP689659.RAm8v8st_M88pNpC7BL6XBBMlQcJIolEScBeDUJujaCmc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP689659.RAm8v8st_M88pNpC7BL6XBBMlQcJIolEScBeDUJujaCmc130_assertion {
   miriam-gene:668 a ncit:C16612 .
  lld:C0000768 a ncit:C7057 .
  dgn-gda:DGNa43cf6cf8ceffa76c8d852ca3ebc1faa sio:SIO_000628 miriam-gene:668 , lld:C0000768 ;
    a sio:SIO_001121 .
}
dgn-np:NP689659.RAm8v8st_M88pNpC7BL6XBBMlQcJIolEScBeDUJujaCmc130_provenance {
   dgn-np:NP689659.RAm8v8st_M88pNpC7BL6XBBMlQcJIolEScBeDUJujaCmc130_assertion dcterms:description "[Mutations in FOXL2 are known to cause blepharophimosis syndrome (BPES), an autosomal dominant eyelid malformation associated (type I) or not (type II) with ovarian dysfunction, leading to premature ovarian failure (POF).]. 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:18726931 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP689659.RAm8v8st_M88pNpC7BL6XBBMlQcJIolEScBeDUJujaCmc130_publicationInfo {
   this: dcterms:created "2016-05-13T12:46:57+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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}