@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP240656.RArYOBDbDCZ03WvABxPqoInmlDEoe7vO5Pd0_K6n6vdvM> .
@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:NP240656.RArYOBDbDCZ03WvABxPqoInmlDEoe7vO5Pd0_K6n6vdvM130_head {
  this: np:hasAssertion dgn-np:NP240656.RArYOBDbDCZ03WvABxPqoInmlDEoe7vO5Pd0_K6n6vdvM130_assertion;
    np:hasProvenance dgn-np:NP240656.RArYOBDbDCZ03WvABxPqoInmlDEoe7vO5Pd0_K6n6vdvM130_provenance;
    np:hasPublicationInfo dgn-np:NP240656.RArYOBDbDCZ03WvABxPqoInmlDEoe7vO5Pd0_K6n6vdvM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP240656.RArYOBDbDCZ03WvABxPqoInmlDEoe7vO5Pd0_K6n6vdvM130_assertion a np:Assertion .
  
  dgn-np:NP240656.RArYOBDbDCZ03WvABxPqoInmlDEoe7vO5Pd0_K6n6vdvM130_provenance a np:Provenance .
  
  dgn-np:NP240656.RArYOBDbDCZ03WvABxPqoInmlDEoe7vO5Pd0_K6n6vdvM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP240656.RArYOBDbDCZ03WvABxPqoInmlDEoe7vO5Pd0_K6n6vdvM130_assertion {
  miriam-gene:7959 a ncit:C16612 .
  
  lld:C0007124 a ncit:C7057 .
  
  dgn-gda:DGN598ef9e6a40e3c529bec5e273d1e7587 sio:SIO_000628 miriam-gene:7959, lld:C0007124;
    a sio:SIO_001121 .
}

dgn-np:NP240656.RArYOBDbDCZ03WvABxPqoInmlDEoe7vO5Pd0_K6n6vdvM130_provenance {
  dgn-np:NP240656.RArYOBDbDCZ03WvABxPqoInmlDEoe7vO5Pd0_K6n6vdvM130_assertion dcterms:description
      "[Four groups samples, including 40 cases of usual ductal hyperplasia (UDH), 40 cases of atypical ductal hyperplasia (ADH), 29 cases of flat epithelia atypia (FEA), and 40 cases of ductal carcinoma in situ (DCIS) were selected for analysis.]. 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:18425676;
    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:NP240656.RArYOBDbDCZ03WvABxPqoInmlDEoe7vO5Pd0_K6n6vdvM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:14+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" .
}