@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP518685.RAZeZCdhAlQZQZCBUFF_uueW7JdoP639s0ZWJXaRkUYO0> .
@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:NP518685.RAZeZCdhAlQZQZCBUFF_uueW7JdoP639s0ZWJXaRkUYO0130_head {
  this: np:hasAssertion dgn-np:NP518685.RAZeZCdhAlQZQZCBUFF_uueW7JdoP639s0ZWJXaRkUYO0130_assertion;
    np:hasProvenance dgn-np:NP518685.RAZeZCdhAlQZQZCBUFF_uueW7JdoP639s0ZWJXaRkUYO0130_provenance;
    np:hasPublicationInfo dgn-np:NP518685.RAZeZCdhAlQZQZCBUFF_uueW7JdoP639s0ZWJXaRkUYO0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP518685.RAZeZCdhAlQZQZCBUFF_uueW7JdoP639s0ZWJXaRkUYO0130_assertion a np:Assertion .
  
  dgn-np:NP518685.RAZeZCdhAlQZQZCBUFF_uueW7JdoP639s0ZWJXaRkUYO0130_provenance a np:Provenance .
  
  dgn-np:NP518685.RAZeZCdhAlQZQZCBUFF_uueW7JdoP639s0ZWJXaRkUYO0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP518685.RAZeZCdhAlQZQZCBUFF_uueW7JdoP639s0ZWJXaRkUYO0130_assertion {
  miriam-gene:6422 a ncit:C16612 .
  
  lld:C0678222 a ncit:C7057 .
  
  dgn-gda:DGN3559273b9baa887afcf761ca645d08a1 sio:SIO_000628 miriam-gene:6422, lld:C0678222;
    a sio:SIO_001121 .
}

dgn-np:NP518685.RAZeZCdhAlQZQZCBUFF_uueW7JdoP639s0ZWJXaRkUYO0130_provenance {
  dgn-np:NP518685.RAZeZCdhAlQZQZCBUFF_uueW7JdoP639s0ZWJXaRkUYO0130_assertion dcterms:description
      "[Our results indicate that promoter hypermethylation is the predominant mechanism of SFRP1 gene silencing in human breast cancer and that SFRP1 gene inactivation in breast cancer is associated with unfavourable prognosis.]. 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:16449975;
    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:NP518685.RAZeZCdhAlQZQZCBUFF_uueW7JdoP639s0ZWJXaRkUYO0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:09+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" .
}