@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP270464.RAKkCWL616zoChJzqkCQumueuY0izRgPRbv5u3GqS0ry0> .
@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:NP270464.RAKkCWL616zoChJzqkCQumueuY0izRgPRbv5u3GqS0ry0130_head {
   this: np:hasAssertion dgn-np:NP270464.RAKkCWL616zoChJzqkCQumueuY0izRgPRbv5u3GqS0ry0130_assertion ;
    np:hasProvenance dgn-np:NP270464.RAKkCWL616zoChJzqkCQumueuY0izRgPRbv5u3GqS0ry0130_provenance ;
    np:hasPublicationInfo dgn-np:NP270464.RAKkCWL616zoChJzqkCQumueuY0izRgPRbv5u3GqS0ry0130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP270464.RAKkCWL616zoChJzqkCQumueuY0izRgPRbv5u3GqS0ry0130_assertion a np:Assertion .
  dgn-np:NP270464.RAKkCWL616zoChJzqkCQumueuY0izRgPRbv5u3GqS0ry0130_provenance a np:Provenance .
  dgn-np:NP270464.RAKkCWL616zoChJzqkCQumueuY0izRgPRbv5u3GqS0ry0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP270464.RAKkCWL616zoChJzqkCQumueuY0izRgPRbv5u3GqS0ry0130_assertion {
   miriam-gene:668 a ncit:C16612 .
  lld:C1401084 a ncit:C7057 .
  dgn-gda:DGNdaa2016a2f461b2b99a6827d57547593 sio:SIO_000628 miriam-gene:668 , lld:C1401084 ;
    a sio:SIO_001121 .
}
dgn-np:NP270464.RAKkCWL616zoChJzqkCQumueuY0izRgPRbv5u3GqS0ry0130_provenance {
   dgn-np:NP270464.RAKkCWL616zoChJzqkCQumueuY0izRgPRbv5u3GqS0ry0130_assertion dcterms:description "[This report shows the importance of family history and genetic analysis in the evaluation of patients with POF and corroborates the relationship between mutations on the FOXL2 gene and ovarian insufficiency.]. 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:19969293 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP270464.RAKkCWL616zoChJzqkCQumueuY0izRgPRbv5u3GqS0ry0130_publicationInfo {
   this: dcterms:created "2015-08-25T14:40:14+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" .
}