@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP439149.RATx2Pm6qu9Vjkes89j8kQRGne9IVMIeEqrHTVENc0d2I> .
@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:NP439149.RATx2Pm6qu9Vjkes89j8kQRGne9IVMIeEqrHTVENc0d2I130_head {
  this: np:hasAssertion dgn-np:NP439149.RATx2Pm6qu9Vjkes89j8kQRGne9IVMIeEqrHTVENc0d2I130_assertion;
    np:hasProvenance dgn-np:NP439149.RATx2Pm6qu9Vjkes89j8kQRGne9IVMIeEqrHTVENc0d2I130_provenance;
    np:hasPublicationInfo dgn-np:NP439149.RATx2Pm6qu9Vjkes89j8kQRGne9IVMIeEqrHTVENc0d2I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP439149.RATx2Pm6qu9Vjkes89j8kQRGne9IVMIeEqrHTVENc0d2I130_assertion a np:Assertion .
  
  dgn-np:NP439149.RATx2Pm6qu9Vjkes89j8kQRGne9IVMIeEqrHTVENc0d2I130_provenance a np:Provenance .
  
  dgn-np:NP439149.RATx2Pm6qu9Vjkes89j8kQRGne9IVMIeEqrHTVENc0d2I130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP439149.RATx2Pm6qu9Vjkes89j8kQRGne9IVMIeEqrHTVENc0d2I130_assertion {
  miriam-gene:668 a ncit:C16612 .
  
  lld:C0154208 a ncit:C7057 .
  
  dgn-gda:DGNfd01e06e6d91f2041fb1000103003740 sio:SIO_000628 miriam-gene:668, lld:C0154208;
    a sio:SIO_001121 .
}

dgn-np:NP439149.RATx2Pm6qu9Vjkes89j8kQRGne9IVMIeEqrHTVENc0d2I130_provenance {
  dgn-np:NP439149.RATx2Pm6qu9Vjkes89j8kQRGne9IVMIeEqrHTVENc0d2I130_assertion dcterms:description
      "[In contrast to known FOXL2 mutations with polyalanine expansions and association with BPES type II, clinical aspects of our girl may indicate some degree of ovarian dysfunction that might finally lead to BPES type I with premature ovarian failure.]. 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:16131596;
    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:NP439149.RATx2Pm6qu9Vjkes89j8kQRGne9IVMIeEqrHTVENc0d2I130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:20+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" .
}