@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP302609.RADML5xdoKlEGz5gBnXJpPgZLDN1s1eqlLtABbqlJ3dVo> .
@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:NP302609.RADML5xdoKlEGz5gBnXJpPgZLDN1s1eqlLtABbqlJ3dVo130_head {
  this: np:hasAssertion dgn-np:NP302609.RADML5xdoKlEGz5gBnXJpPgZLDN1s1eqlLtABbqlJ3dVo130_assertion;
    np:hasProvenance dgn-np:NP302609.RADML5xdoKlEGz5gBnXJpPgZLDN1s1eqlLtABbqlJ3dVo130_provenance;
    np:hasPublicationInfo dgn-np:NP302609.RADML5xdoKlEGz5gBnXJpPgZLDN1s1eqlLtABbqlJ3dVo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP302609.RADML5xdoKlEGz5gBnXJpPgZLDN1s1eqlLtABbqlJ3dVo130_assertion a np:Assertion .
  
  dgn-np:NP302609.RADML5xdoKlEGz5gBnXJpPgZLDN1s1eqlLtABbqlJ3dVo130_provenance a np:Provenance .
  
  dgn-np:NP302609.RADML5xdoKlEGz5gBnXJpPgZLDN1s1eqlLtABbqlJ3dVo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP302609.RADML5xdoKlEGz5gBnXJpPgZLDN1s1eqlLtABbqlJ3dVo130_assertion {
  miriam-gene:580 a ncit:C16612 .
  
  lld:C0206681 a ncit:C7057 .
  
  dgn-gda:DGNccc64ab304c25462acb598a4135fe69f sio:SIO_000628 miriam-gene:580, lld:C0206681;
    a sio:SIO_001121 .
}

dgn-np:NP302609.RADML5xdoKlEGz5gBnXJpPgZLDN1s1eqlLtABbqlJ3dVo130_provenance {
  dgn-np:NP302609.RADML5xdoKlEGz5gBnXJpPgZLDN1s1eqlLtABbqlJ3dVo130_assertion dcterms:description
      "[Expression of NH(2) terminally truncated BARD1 was correlated with advanced stage of cancer, and expression of spliced isoforms was typical for clear cell carcinoma, the ovarian cancer with worst prognosis, suggesting a role of BARD1 isoforms in cancer progression.]. 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:18089818;
    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:NP302609.RADML5xdoKlEGz5gBnXJpPgZLDN1s1eqlLtABbqlJ3dVo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:54+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" .
}