@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP953999.RAyBNoegelhHtGm7EIdl7DoLJY4HTlAxMIZklvccMyupc> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP953999.RAyBNoegelhHtGm7EIdl7DoLJY4HTlAxMIZklvccMyupc130_head {
  this: np:hasAssertion dgn-np:NP953999.RAyBNoegelhHtGm7EIdl7DoLJY4HTlAxMIZklvccMyupc130_assertion;
    np:hasProvenance dgn-np:NP953999.RAyBNoegelhHtGm7EIdl7DoLJY4HTlAxMIZklvccMyupc130_provenance;
    np:hasPublicationInfo dgn-np:NP953999.RAyBNoegelhHtGm7EIdl7DoLJY4HTlAxMIZklvccMyupc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP953999.RAyBNoegelhHtGm7EIdl7DoLJY4HTlAxMIZklvccMyupc130_assertion a np:Assertion .
  
  dgn-np:NP953999.RAyBNoegelhHtGm7EIdl7DoLJY4HTlAxMIZklvccMyupc130_provenance a np:Provenance .
  
  dgn-np:NP953999.RAyBNoegelhHtGm7EIdl7DoLJY4HTlAxMIZklvccMyupc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP953999.RAyBNoegelhHtGm7EIdl7DoLJY4HTlAxMIZklvccMyupc130_assertion {
  miriam-gene:1632 a ncit:C16612 .
  
  lld:C1449563 a ncit:C7057 .
  
  dgn-gda:DGN4589730e6e47198aaf9a0296b45d26d8 sio:SIO_000628 miriam-gene:1632, lld:C1449563;
    a sio:SIO_001121 .
}

dgn-np:NP953999.RAyBNoegelhHtGm7EIdl7DoLJY4HTlAxMIZklvccMyupc130_provenance {
  dgn-np:NP953999.RAyBNoegelhHtGm7EIdl7DoLJY4HTlAxMIZklvccMyupc130_assertion dcterms:description
      "[To determine whether synchronously diagnosed ipsilateral DCI and IDCs have modal populations with distinct repertoires of gene copy number aberrations and mutations in common oncogenes, matched frozen samples of DCIS and IDC were retrieved from 13 patients and subjected to microarray-based comparative genomic hybridization (aCGH) and Sequenom MassARRAY (Oncocarta v 1.0 panel).]. 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:22252965;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP953999.RAyBNoegelhHtGm7EIdl7DoLJY4HTlAxMIZklvccMyupc130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:57+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}