@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP705343.RAOWIc0zt0Yftnh5opPvHpGbtw4eSY66tThltolL9FXNk> .
@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:NP705343.RAOWIc0zt0Yftnh5opPvHpGbtw4eSY66tThltolL9FXNk130_head {
  this: np:hasAssertion dgn-np:NP705343.RAOWIc0zt0Yftnh5opPvHpGbtw4eSY66tThltolL9FXNk130_assertion;
    np:hasProvenance dgn-np:NP705343.RAOWIc0zt0Yftnh5opPvHpGbtw4eSY66tThltolL9FXNk130_provenance;
    np:hasPublicationInfo dgn-np:NP705343.RAOWIc0zt0Yftnh5opPvHpGbtw4eSY66tThltolL9FXNk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP705343.RAOWIc0zt0Yftnh5opPvHpGbtw4eSY66tThltolL9FXNk130_assertion a np:Assertion .
  
  dgn-np:NP705343.RAOWIc0zt0Yftnh5opPvHpGbtw4eSY66tThltolL9FXNk130_provenance a np:Provenance .
  
  dgn-np:NP705343.RAOWIc0zt0Yftnh5opPvHpGbtw4eSY66tThltolL9FXNk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP705343.RAOWIc0zt0Yftnh5opPvHpGbtw4eSY66tThltolL9FXNk130_assertion {
  miriam-gene:57026 a ncit:C16612 .
  
  lld:C0007124 a ncit:C7057 .
  
  dgn-gda:DGN157ae722cb12bf1cdf2fb9f72e57932b sio:SIO_000628 miriam-gene:57026, lld:C0007124;
    a sio:SIO_001121 .
}

dgn-np:NP705343.RAOWIc0zt0Yftnh5opPvHpGbtw4eSY66tThltolL9FXNk130_provenance {
  dgn-np:NP705343.RAOWIc0zt0Yftnh5opPvHpGbtw4eSY66tThltolL9FXNk130_assertion dcterms:description
      "[However, CIN might also cause genetic heterogeneity, which was revealed by the findings that LOH at some markers was observed only in the component of ductal carcinoma in situ but not in the invasive component of the same tumors.]. 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:10919664;
    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:NP705343.RAOWIc0zt0Yftnh5opPvHpGbtw4eSY66tThltolL9FXNk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:08+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" .
}