@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP84620.RArwmRHFZ4HVAh67k1iuYHvF98z21sEmTvM8_67fWI6Is> .
@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:NP84620.RArwmRHFZ4HVAh67k1iuYHvF98z21sEmTvM8_67fWI6Is130_head {
  this: np:hasAssertion dgn-np:NP84620.RArwmRHFZ4HVAh67k1iuYHvF98z21sEmTvM8_67fWI6Is130_assertion;
    np:hasProvenance dgn-np:NP84620.RArwmRHFZ4HVAh67k1iuYHvF98z21sEmTvM8_67fWI6Is130_provenance;
    np:hasPublicationInfo dgn-np:NP84620.RArwmRHFZ4HVAh67k1iuYHvF98z21sEmTvM8_67fWI6Is130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP84620.RArwmRHFZ4HVAh67k1iuYHvF98z21sEmTvM8_67fWI6Is130_assertion a np:Assertion .
  
  dgn-np:NP84620.RArwmRHFZ4HVAh67k1iuYHvF98z21sEmTvM8_67fWI6Is130_provenance a np:Provenance .
  
  dgn-np:NP84620.RArwmRHFZ4HVAh67k1iuYHvF98z21sEmTvM8_67fWI6Is130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP84620.RArwmRHFZ4HVAh67k1iuYHvF98z21sEmTvM8_67fWI6Is130_assertion {
  miriam-gene:407046 a ncit:C16612 .
  
  lld:C1140680 a ncit:C7057 .
  
  dgn-gda:DGNb94a036d812c541f133538fc5ff07428 sio:SIO_000628 miriam-gene:407046, lld:C1140680;
    a sio:SIO_001122 .
}

dgn-np:NP84620.RArwmRHFZ4HVAh67k1iuYHvF98z21sEmTvM8_67fWI6Is130_provenance {
  dgn-np:NP84620.RArwmRHFZ4HVAh67k1iuYHvF98z21sEmTvM8_67fWI6Is130_assertion dcterms:description
      "[Our findings suggest that there are novel genetic variants in miRNA genes, and those certain genetic variants in miRNA genes can affect the expression of mature miRNAs and, consequently, might alter the regulation of TSGs or oncogenes. Additionally, the variant might be potentially associated with the development of familial ovarian cancer.]. 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:20167074;
    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:NP84620.RArwmRHFZ4HVAh67k1iuYHvF98z21sEmTvM8_67fWI6Is130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:41+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" .
}