@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP208911.RAkq_F2n7ujnDOcdzwCSD-eo6JXUDRLOF60tUr4u84xLc> .
@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:NP208911.RAkq_F2n7ujnDOcdzwCSD-eo6JXUDRLOF60tUr4u84xLc130_head {
  this: np:hasAssertion dgn-np:NP208911.RAkq_F2n7ujnDOcdzwCSD-eo6JXUDRLOF60tUr4u84xLc130_assertion;
    np:hasProvenance dgn-np:NP208911.RAkq_F2n7ujnDOcdzwCSD-eo6JXUDRLOF60tUr4u84xLc130_provenance;
    np:hasPublicationInfo dgn-np:NP208911.RAkq_F2n7ujnDOcdzwCSD-eo6JXUDRLOF60tUr4u84xLc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP208911.RAkq_F2n7ujnDOcdzwCSD-eo6JXUDRLOF60tUr4u84xLc130_assertion a np:Assertion .
  
  dgn-np:NP208911.RAkq_F2n7ujnDOcdzwCSD-eo6JXUDRLOF60tUr4u84xLc130_provenance a np:Provenance .
  
  dgn-np:NP208911.RAkq_F2n7ujnDOcdzwCSD-eo6JXUDRLOF60tUr4u84xLc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP208911.RAkq_F2n7ujnDOcdzwCSD-eo6JXUDRLOF60tUr4u84xLc130_assertion {
  miriam-gene:3342 a ncit:C16612 .
  
  lld:C0007124 a ncit:C7057 .
  
  dgn-gda:DGNcf4c3eb598cfdaf3792d8091d81bc358 sio:SIO_000628 miriam-gene:3342, lld:C0007124;
    a sio:SIO_001121 .
}

dgn-np:NP208911.RAkq_F2n7ujnDOcdzwCSD-eo6JXUDRLOF60tUr4u84xLc130_provenance {
  dgn-np:NP208911.RAkq_F2n7ujnDOcdzwCSD-eo6JXUDRLOF60tUr4u84xLc130_assertion dcterms:description
      "[Comparative genomic hybridization (CGH) was used to compare chromosomal alterations in 18 initial DCIS lesions (presenting in the absence of invasive disease) and in their subsequent ipsilateral DCIS recurrences (detected from 16 months to 9.3 years later).]. 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:10675380;
    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:NP208911.RAkq_F2n7ujnDOcdzwCSD-eo6JXUDRLOF60tUr4u84xLc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:55+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" .
}