@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP90979.RA3elTqfx1QZKVZC3ngaQ3y4QLb8SHYcqaSJJ6GkL2Ta4> .
@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:NP90979.RA3elTqfx1QZKVZC3ngaQ3y4QLb8SHYcqaSJJ6GkL2Ta4130_head {
  this: np:hasAssertion dgn-np:NP90979.RA3elTqfx1QZKVZC3ngaQ3y4QLb8SHYcqaSJJ6GkL2Ta4130_assertion;
    np:hasProvenance dgn-np:NP90979.RA3elTqfx1QZKVZC3ngaQ3y4QLb8SHYcqaSJJ6GkL2Ta4130_provenance;
    np:hasPublicationInfo dgn-np:NP90979.RA3elTqfx1QZKVZC3ngaQ3y4QLb8SHYcqaSJJ6GkL2Ta4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP90979.RA3elTqfx1QZKVZC3ngaQ3y4QLb8SHYcqaSJJ6GkL2Ta4130_assertion a np:Assertion .
  
  dgn-np:NP90979.RA3elTqfx1QZKVZC3ngaQ3y4QLb8SHYcqaSJJ6GkL2Ta4130_provenance a np:Provenance .
  
  dgn-np:NP90979.RA3elTqfx1QZKVZC3ngaQ3y4QLb8SHYcqaSJJ6GkL2Ta4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP90979.RA3elTqfx1QZKVZC3ngaQ3y4QLb8SHYcqaSJJ6GkL2Ta4130_assertion {
  miriam-gene:842 a ncit:C16612 .
  
  lld:C0279628 a ncit:C7057 .
  
  dgn-gda:DGN03495c21fc256f03329f2d0452df1614 sio:SIO_000628 miriam-gene:842, lld:C0279628;
    a sio:SIO_001122 .
}

dgn-np:NP90979.RA3elTqfx1QZKVZC3ngaQ3y4QLb8SHYcqaSJJ6GkL2Ta4130_provenance {
  dgn-np:NP90979.RA3elTqfx1QZKVZC3ngaQ3y4QLb8SHYcqaSJJ6GkL2Ta4130_assertion dcterms:description
      "[In conclusion, this study suggests that the genetic variants of CASP7 and CASP9 in the apoptosis pathway may be important predictive markers for EA susceptibility and that PGR in the sex hormone signaling pathway may be associated with the gender differences in EA risk.]. 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:20453000;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP90979.RA3elTqfx1QZKVZC3ngaQ3y4QLb8SHYcqaSJJ6GkL2Ta4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:45+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" .
}