@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP585427.RAEz8dOOtQhHF1tM92c819dkXM6aNZnEUgjPrf2FP62qY> .
@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:NP585427.RAEz8dOOtQhHF1tM92c819dkXM6aNZnEUgjPrf2FP62qY130_head {
  this: np:hasAssertion dgn-np:NP585427.RAEz8dOOtQhHF1tM92c819dkXM6aNZnEUgjPrf2FP62qY130_assertion;
    np:hasProvenance dgn-np:NP585427.RAEz8dOOtQhHF1tM92c819dkXM6aNZnEUgjPrf2FP62qY130_provenance;
    np:hasPublicationInfo dgn-np:NP585427.RAEz8dOOtQhHF1tM92c819dkXM6aNZnEUgjPrf2FP62qY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP585427.RAEz8dOOtQhHF1tM92c819dkXM6aNZnEUgjPrf2FP62qY130_assertion a np:Assertion .
  
  dgn-np:NP585427.RAEz8dOOtQhHF1tM92c819dkXM6aNZnEUgjPrf2FP62qY130_provenance a np:Provenance .
  
  dgn-np:NP585427.RAEz8dOOtQhHF1tM92c819dkXM6aNZnEUgjPrf2FP62qY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP585427.RAEz8dOOtQhHF1tM92c819dkXM6aNZnEUgjPrf2FP62qY130_assertion {
  miriam-gene:4000 a ncit:C16612 .
  
  lld:C0678222 a ncit:C7057 .
  
  dgn-gda:DGN1dc63b548822314a351e418fcad8f72e sio:SIO_000628 miriam-gene:4000, lld:C0678222;
    a sio:SIO_001121 .
}

dgn-np:NP585427.RAEz8dOOtQhHF1tM92c819dkXM6aNZnEUgjPrf2FP62qY130_provenance {
  dgn-np:NP585427.RAEz8dOOtQhHF1tM92c819dkXM6aNZnEUgjPrf2FP62qY130_assertion dcterms:description
      "[To assess the molecular alterations associated with these breast cancer subtypes, we conducted a whole-genome study of 166 archival estrogen receptor (ER)-positive tumors (89 IDC and 77 ILC) using the Affymetrix GeneChip(R) Mapping 10K Array to identify sites of loss of heterozygosity (LOH) that either distinguished, or were shared by, the two phenotypes.]. 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:18720524;
    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:NP585427.RAEz8dOOtQhHF1tM92c819dkXM6aNZnEUgjPrf2FP62qY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:52+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" .
}