@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP265072.RAev81-bFP_x4U_2umG9QBYTyaSykslkXBCkPU-sJ1l8c> .
@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:NP265072.RAev81-bFP_x4U_2umG9QBYTyaSykslkXBCkPU-sJ1l8c130_head {
  this: np:hasAssertion dgn-np:NP265072.RAev81-bFP_x4U_2umG9QBYTyaSykslkXBCkPU-sJ1l8c130_assertion;
    np:hasProvenance dgn-np:NP265072.RAev81-bFP_x4U_2umG9QBYTyaSykslkXBCkPU-sJ1l8c130_provenance;
    np:hasPublicationInfo dgn-np:NP265072.RAev81-bFP_x4U_2umG9QBYTyaSykslkXBCkPU-sJ1l8c130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP265072.RAev81-bFP_x4U_2umG9QBYTyaSykslkXBCkPU-sJ1l8c130_assertion a np:Assertion .
  
  dgn-np:NP265072.RAev81-bFP_x4U_2umG9QBYTyaSykslkXBCkPU-sJ1l8c130_provenance a np:Provenance .
  
  dgn-np:NP265072.RAev81-bFP_x4U_2umG9QBYTyaSykslkXBCkPU-sJ1l8c130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP265072.RAev81-bFP_x4U_2umG9QBYTyaSykslkXBCkPU-sJ1l8c130_assertion {
  miriam-gene:3576 a ncit:C16612 .
  
  lld:C0678222 a ncit:C7057 .
  
  dgn-gda:DGNfa9039527735f8c5f858a2b2ee1ae9c5 sio:SIO_000628 miriam-gene:3576, lld:C0678222;
    a sio:SIO_001121 .
}

dgn-np:NP265072.RAev81-bFP_x4U_2umG9QBYTyaSykslkXBCkPU-sJ1l8c130_provenance {
  dgn-np:NP265072.RAev81-bFP_x4U_2umG9QBYTyaSykslkXBCkPU-sJ1l8c130_assertion dcterms:description
      "[In summary, i) routine quantitative DNA methylation assessment in NAF and MD samples is possible, and ii) genes hypermethylated in malignant breast tissue are also altered in matched NAF and in MD samples, and may be useful to assist in early breast cancer detection.]. 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:19618401;
    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:NP265072.RAev81-bFP_x4U_2umG9QBYTyaSykslkXBCkPU-sJ1l8c130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:28+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" .
}