@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP387866.RAhApJrv0r1MVR8E2sbt87ccvZW-9ng2eqLh163S-4z3k> .
@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:NP387866.RAhApJrv0r1MVR8E2sbt87ccvZW-9ng2eqLh163S-4z3k130_head {
  this: np:hasAssertion dgn-np:NP387866.RAhApJrv0r1MVR8E2sbt87ccvZW-9ng2eqLh163S-4z3k130_assertion;
    np:hasProvenance dgn-np:NP387866.RAhApJrv0r1MVR8E2sbt87ccvZW-9ng2eqLh163S-4z3k130_provenance;
    np:hasPublicationInfo dgn-np:NP387866.RAhApJrv0r1MVR8E2sbt87ccvZW-9ng2eqLh163S-4z3k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP387866.RAhApJrv0r1MVR8E2sbt87ccvZW-9ng2eqLh163S-4z3k130_assertion a np:Assertion .
  
  dgn-np:NP387866.RAhApJrv0r1MVR8E2sbt87ccvZW-9ng2eqLh163S-4z3k130_provenance a np:Provenance .
  
  dgn-np:NP387866.RAhApJrv0r1MVR8E2sbt87ccvZW-9ng2eqLh163S-4z3k130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP387866.RAhApJrv0r1MVR8E2sbt87ccvZW-9ng2eqLh163S-4z3k130_assertion {
  miriam-gene:79184 a ncit:C16612 .
  
  lld:C0678222 a ncit:C7057 .
  
  dgn-gda:DGN8e0802e5fb9691c9ca8609c08db9a707 sio:SIO_000628 miriam-gene:79184, lld:C0678222;
    a sio:SIO_001121 .
}

dgn-np:NP387866.RAhApJrv0r1MVR8E2sbt87ccvZW-9ng2eqLh163S-4z3k130_provenance {
  dgn-np:NP387866.RAhApJrv0r1MVR8E2sbt87ccvZW-9ng2eqLh163S-4z3k130_assertion dcterms:description
      "[To further elucidate the functional consequence of abnormal BRCC36 expression in breast cancer, we have done in vivo silencing studies using small interfering RNAs targeting BRCC36 in breast cancer cell lines, i.e., MCF-7, ZR-75-1, and T47D.]. 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:16707425;
    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:NP387866.RAhApJrv0r1MVR8E2sbt87ccvZW-9ng2eqLh163S-4z3k130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:51+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>,
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  dgn-void:disgenetrdf pav:version "v2.1.0" .
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