@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP160365.RAkCBH4m2rShXK5meHtAcyJF2esRZqPkY5VYCmo1GMJYE> .
@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:NP160365.RAkCBH4m2rShXK5meHtAcyJF2esRZqPkY5VYCmo1GMJYE130_head {
  this: np:hasAssertion dgn-np:NP160365.RAkCBH4m2rShXK5meHtAcyJF2esRZqPkY5VYCmo1GMJYE130_assertion;
    np:hasProvenance dgn-np:NP160365.RAkCBH4m2rShXK5meHtAcyJF2esRZqPkY5VYCmo1GMJYE130_provenance;
    np:hasPublicationInfo dgn-np:NP160365.RAkCBH4m2rShXK5meHtAcyJF2esRZqPkY5VYCmo1GMJYE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP160365.RAkCBH4m2rShXK5meHtAcyJF2esRZqPkY5VYCmo1GMJYE130_assertion a np:Assertion .
  
  dgn-np:NP160365.RAkCBH4m2rShXK5meHtAcyJF2esRZqPkY5VYCmo1GMJYE130_provenance a np:Provenance .
  
  dgn-np:NP160365.RAkCBH4m2rShXK5meHtAcyJF2esRZqPkY5VYCmo1GMJYE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP160365.RAkCBH4m2rShXK5meHtAcyJF2esRZqPkY5VYCmo1GMJYE130_assertion {
  miriam-gene:5241 a ncit:C16612 .
  
  lld:C0014175 a ncit:C7057 .
  
  dgn-gda:DGN61058f8c0ec82710cae1eb0443e49a25 sio:SIO_000628 miriam-gene:5241, lld:C0014175;
    a sio:SIO_001121 .
}

dgn-np:NP160365.RAkCBH4m2rShXK5meHtAcyJF2esRZqPkY5VYCmo1GMJYE130_provenance {
  dgn-np:NP160365.RAkCBH4m2rShXK5meHtAcyJF2esRZqPkY5VYCmo1GMJYE130_assertion dcterms:description
      "[Because of the crucial role that the progesterone receptor polymorphism PROGINS plays in predisposing women to the development of endometriosis, we hypothesized that this variant may influence critical steps during endometrial cell metabolism that are involved in the pathogenesis of endometriosis.]. 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:19497994;
    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:NP160365.RAkCBH4m2rShXK5meHtAcyJF2esRZqPkY5VYCmo1GMJYE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:26+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" .
}