@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP395255.RABbzz3CjxH75XKHDaIpsvB9ixFtvD1GllZdOtM70_tE4> .
@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:NP395255.RABbzz3CjxH75XKHDaIpsvB9ixFtvD1GllZdOtM70_tE4130_head {
  this: np:hasAssertion dgn-np:NP395255.RABbzz3CjxH75XKHDaIpsvB9ixFtvD1GllZdOtM70_tE4130_assertion;
    np:hasProvenance dgn-np:NP395255.RABbzz3CjxH75XKHDaIpsvB9ixFtvD1GllZdOtM70_tE4130_provenance;
    np:hasPublicationInfo dgn-np:NP395255.RABbzz3CjxH75XKHDaIpsvB9ixFtvD1GllZdOtM70_tE4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP395255.RABbzz3CjxH75XKHDaIpsvB9ixFtvD1GllZdOtM70_tE4130_assertion a np:Assertion .
  
  dgn-np:NP395255.RABbzz3CjxH75XKHDaIpsvB9ixFtvD1GllZdOtM70_tE4130_provenance a np:Provenance .
  
  dgn-np:NP395255.RABbzz3CjxH75XKHDaIpsvB9ixFtvD1GllZdOtM70_tE4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP395255.RABbzz3CjxH75XKHDaIpsvB9ixFtvD1GllZdOtM70_tE4130_assertion {
  miriam-gene:51366 a ncit:C16612 .
  
  lld:C0029925 a ncit:C7057 .
  
  dgn-gda:DGN33b98b2afe8b666fd7f6c66e6f5e6cc0 sio:SIO_000628 miriam-gene:51366, lld:C0029925;
    a sio:SIO_001121 .
}

dgn-np:NP395255.RABbzz3CjxH75XKHDaIpsvB9ixFtvD1GllZdOtM70_tE4130_provenance {
  dgn-np:NP395255.RABbzz3CjxH75XKHDaIpsvB9ixFtvD1GllZdOtM70_tE4130_assertion dcterms:description
      "[AI is likely to represent amplification of the EDD gene locus rather than loss of heterozygosity, as quantitative RT-PCR and immunohistochemistry showed that EDD mRNA and protein are frequently overexpressed in breast and ovarian cancers, while among breast cancer cell lines EDD overexpression and increased gene copy number were correlated.]. 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:12902990;
    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:NP395255.RABbzz3CjxH75XKHDaIpsvB9ixFtvD1GllZdOtM70_tE4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:55+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" .
}