@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP170692.RAA-uJaLYNWLAOZnKtqnrGP6KDdogbzQ5EmFjnG9O6VnI> .
@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:NP170692.RAA-uJaLYNWLAOZnKtqnrGP6KDdogbzQ5EmFjnG9O6VnI130_head {
  this: np:hasAssertion dgn-np:NP170692.RAA-uJaLYNWLAOZnKtqnrGP6KDdogbzQ5EmFjnG9O6VnI130_assertion;
    np:hasProvenance dgn-np:NP170692.RAA-uJaLYNWLAOZnKtqnrGP6KDdogbzQ5EmFjnG9O6VnI130_provenance;
    np:hasPublicationInfo dgn-np:NP170692.RAA-uJaLYNWLAOZnKtqnrGP6KDdogbzQ5EmFjnG9O6VnI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP170692.RAA-uJaLYNWLAOZnKtqnrGP6KDdogbzQ5EmFjnG9O6VnI130_assertion a np:Assertion .
  
  dgn-np:NP170692.RAA-uJaLYNWLAOZnKtqnrGP6KDdogbzQ5EmFjnG9O6VnI130_provenance a np:Provenance .
  
  dgn-np:NP170692.RAA-uJaLYNWLAOZnKtqnrGP6KDdogbzQ5EmFjnG9O6VnI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP170692.RAA-uJaLYNWLAOZnKtqnrGP6KDdogbzQ5EmFjnG9O6VnI130_assertion {
  miriam-gene:5241 a ncit:C16612 .
  
  lld:C0686619 a ncit:C7057 .
  
  dgn-gda:DGNa8ab38e0d5b52a81dc1f0bfbbb5e4ce3 sio:SIO_000628 miriam-gene:5241, lld:C0686619;
    a sio:SIO_001121 .
}

dgn-np:NP170692.RAA-uJaLYNWLAOZnKtqnrGP6KDdogbzQ5EmFjnG9O6VnI130_provenance {
  dgn-np:NP170692.RAA-uJaLYNWLAOZnKtqnrGP6KDdogbzQ5EmFjnG9O6VnI130_assertion dcterms:description
      "[Association of the loss of heterozygosity/allelic imbalance, in both the stroma and epithelium, with presenting clinicopathological features, such as tumor grade, expression status of estrogen receptor and progesterone receptor, human epidermal growth factor receptor 2, clinical stage, and regional lymph node metastasis status.]. 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:17507346;
    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:NP170692.RAA-uJaLYNWLAOZnKtqnrGP6KDdogbzQ5EmFjnG9O6VnI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:32+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" .
}