@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP836373.RALIZ0TonpMXiTHP7AjldRZgvKvc2gbwPX9vLyJm1cOlQ> .
@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:NP836373.RALIZ0TonpMXiTHP7AjldRZgvKvc2gbwPX9vLyJm1cOlQ130_head {
  this: np:hasAssertion dgn-np:NP836373.RALIZ0TonpMXiTHP7AjldRZgvKvc2gbwPX9vLyJm1cOlQ130_assertion;
    np:hasProvenance dgn-np:NP836373.RALIZ0TonpMXiTHP7AjldRZgvKvc2gbwPX9vLyJm1cOlQ130_provenance;
    np:hasPublicationInfo dgn-np:NP836373.RALIZ0TonpMXiTHP7AjldRZgvKvc2gbwPX9vLyJm1cOlQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP836373.RALIZ0TonpMXiTHP7AjldRZgvKvc2gbwPX9vLyJm1cOlQ130_assertion a np:Assertion .
  
  dgn-np:NP836373.RALIZ0TonpMXiTHP7AjldRZgvKvc2gbwPX9vLyJm1cOlQ130_provenance a np:Provenance .
  
  dgn-np:NP836373.RALIZ0TonpMXiTHP7AjldRZgvKvc2gbwPX9vLyJm1cOlQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP836373.RALIZ0TonpMXiTHP7AjldRZgvKvc2gbwPX9vLyJm1cOlQ130_assertion {
  miriam-gene:2099 a ncit:C16612 .
  
  lld:C0025322 a ncit:C7057 .
  
  dgn-gda:DGN81e5fc1b2aa5a695e960d9cf4c7361bf sio:SIO_000628 miriam-gene:2099, lld:C0025322;
    a sio:SIO_001121 .
}

dgn-np:NP836373.RALIZ0TonpMXiTHP7AjldRZgvKvc2gbwPX9vLyJm1cOlQ130_provenance {
  dgn-np:NP836373.RALIZ0TonpMXiTHP7AjldRZgvKvc2gbwPX9vLyJm1cOlQ130_assertion dcterms:description
      "[Because an interaction between CYP19A1 and ESR1 may play a key role in determining the level of circulating E2 by way of the hypothalamus-hypophysis-ovarian axis, the effect of single nucleotide polymorphism (SNP)-SNP interactions between CYP19A1 and ESR1 on the development of premature ovarian failure (POF) was investigated by comparing the polymorphisms of 98 patients with POF and 218 matched controls of Korean ethnicity.]. 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:20797716;
    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:NP836373.RALIZ0TonpMXiTHP7AjldRZgvKvc2gbwPX9vLyJm1cOlQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:31+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" .
}