@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP356377.RAreTH_PDU-P5rDlYNMKhS0yl9cae_f2F7cQ4fwS1yW8M> .
@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:NP356377.RAreTH_PDU-P5rDlYNMKhS0yl9cae_f2F7cQ4fwS1yW8M130_head {
  this: np:hasAssertion dgn-np:NP356377.RAreTH_PDU-P5rDlYNMKhS0yl9cae_f2F7cQ4fwS1yW8M130_assertion;
    np:hasProvenance dgn-np:NP356377.RAreTH_PDU-P5rDlYNMKhS0yl9cae_f2F7cQ4fwS1yW8M130_provenance;
    np:hasPublicationInfo dgn-np:NP356377.RAreTH_PDU-P5rDlYNMKhS0yl9cae_f2F7cQ4fwS1yW8M130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP356377.RAreTH_PDU-P5rDlYNMKhS0yl9cae_f2F7cQ4fwS1yW8M130_assertion a np:Assertion .
  
  dgn-np:NP356377.RAreTH_PDU-P5rDlYNMKhS0yl9cae_f2F7cQ4fwS1yW8M130_provenance a np:Provenance .
  
  dgn-np:NP356377.RAreTH_PDU-P5rDlYNMKhS0yl9cae_f2F7cQ4fwS1yW8M130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP356377.RAreTH_PDU-P5rDlYNMKhS0yl9cae_f2F7cQ4fwS1yW8M130_assertion {
  miriam-gene:7431 a ncit:C16612 .
  
  lld:C0007124 a ncit:C7057 .
  
  dgn-gda:DGN277ef3a9b4b87b6854b9d361ae69a3a4 sio:SIO_000628 miriam-gene:7431, lld:C0007124;
    a sio:SIO_001121 .
}

dgn-np:NP356377.RAreTH_PDU-P5rDlYNMKhS0yl9cae_f2F7cQ4fwS1yW8M130_provenance {
  dgn-np:NP356377.RAreTH_PDU-P5rDlYNMKhS0yl9cae_f2F7cQ4fwS1yW8M130_assertion dcterms:description
      "[Thirteen cases (eight DCIS and five IDC) showed expression of CK8, CK14, CK18, vimentin, and EGFR, consistent with a stem cell phenotype, whereas 44 cases (27 DCIS and 17 IDC) showed expression of CK8 and CK1, weak or negative expression of CK18, but were negative for vimentin and EGFR, consistent with a luminal cell phenotype.]. 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:12037031;
    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:NP356377.RAreTH_PDU-P5rDlYNMKhS0yl9cae_f2F7cQ4fwS1yW8M130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:26+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" .
}