@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP461126.RAd82YtWFza0cu44bnxvxZOig62-LHBzqIXTkrrszqBNw> .
@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:NP461126.RAd82YtWFza0cu44bnxvxZOig62-LHBzqIXTkrrszqBNw130_head {
  this: np:hasAssertion dgn-np:NP461126.RAd82YtWFza0cu44bnxvxZOig62-LHBzqIXTkrrszqBNw130_assertion;
    np:hasProvenance dgn-np:NP461126.RAd82YtWFza0cu44bnxvxZOig62-LHBzqIXTkrrszqBNw130_provenance;
    np:hasPublicationInfo dgn-np:NP461126.RAd82YtWFza0cu44bnxvxZOig62-LHBzqIXTkrrszqBNw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP461126.RAd82YtWFza0cu44bnxvxZOig62-LHBzqIXTkrrszqBNw130_assertion a np:Assertion .
  
  dgn-np:NP461126.RAd82YtWFza0cu44bnxvxZOig62-LHBzqIXTkrrszqBNw130_provenance a np:Provenance .
  
  dgn-np:NP461126.RAd82YtWFza0cu44bnxvxZOig62-LHBzqIXTkrrszqBNw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP461126.RAd82YtWFza0cu44bnxvxZOig62-LHBzqIXTkrrszqBNw130_assertion {
  miriam-gene:4000 a ncit:C16612 .
  
  lld:C0006142 a ncit:C7057 .
  
  dgn-gda:DGN78fded3102bff5b62758ed9fa27704c1 sio:SIO_000628 miriam-gene:4000, lld:C0006142;
    a sio:SIO_001121 .
}

dgn-np:NP461126.RAd82YtWFza0cu44bnxvxZOig62-LHBzqIXTkrrszqBNw130_provenance {
  dgn-np:NP461126.RAd82YtWFza0cu44bnxvxZOig62-LHBzqIXTkrrszqBNw130_assertion dcterms:description
      "[Although there was only a slight agreement of DNA copy number alterations between the primary tumor and the blood samples, the blood cell copy number variation may have some clinical significance as compared to the primary tumor in IDC breast cancer patients.]. 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:20409316;
    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:NP461126.RAd82YtWFza0cu44bnxvxZOig62-LHBzqIXTkrrszqBNw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:34+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" .
}