@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP628518.RAATMENqdj1aQDaz4rZPeQ2_xmPxC6ZQOZE_kFqHOt6qk> .
@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:NP628518.RAATMENqdj1aQDaz4rZPeQ2_xmPxC6ZQOZE_kFqHOt6qk130_head {
  this: np:hasAssertion dgn-np:NP628518.RAATMENqdj1aQDaz4rZPeQ2_xmPxC6ZQOZE_kFqHOt6qk130_assertion;
    np:hasProvenance dgn-np:NP628518.RAATMENqdj1aQDaz4rZPeQ2_xmPxC6ZQOZE_kFqHOt6qk130_provenance;
    np:hasPublicationInfo dgn-np:NP628518.RAATMENqdj1aQDaz4rZPeQ2_xmPxC6ZQOZE_kFqHOt6qk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP628518.RAATMENqdj1aQDaz4rZPeQ2_xmPxC6ZQOZE_kFqHOt6qk130_assertion a np:Assertion .
  
  dgn-np:NP628518.RAATMENqdj1aQDaz4rZPeQ2_xmPxC6ZQOZE_kFqHOt6qk130_provenance a np:Provenance .
  
  dgn-np:NP628518.RAATMENqdj1aQDaz4rZPeQ2_xmPxC6ZQOZE_kFqHOt6qk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP628518.RAATMENqdj1aQDaz4rZPeQ2_xmPxC6ZQOZE_kFqHOt6qk130_assertion {
  miriam-gene:6657 a ncit:C16612 .
  
  lld:C0007099 a ncit:C7057 .
  
  dgn-gda:DGN7934bcddb8d733b73e09f9b7e31d1f74 sio:SIO_000628 miriam-gene:6657, lld:C0007099;
    a sio:SIO_001121 .
}

dgn-np:NP628518.RAATMENqdj1aQDaz4rZPeQ2_xmPxC6ZQOZE_kFqHOt6qk130_provenance {
  dgn-np:NP628518.RAATMENqdj1aQDaz4rZPeQ2_xmPxC6ZQOZE_kFqHOt6qk130_assertion dcterms:description
      "[Immunohistochemical analysis of various histological lung tissue specimens demonstrated marked nuclear SOX2 protein expression in all normal bronchial epithelia, alveolar bronchiolization structures and premalignant lesions in SCC development (hyperplasia, dysplasia and carcinoma in situ) and absence of expression in all normal alveoli and atypical adenomatous hyperplasias.]. 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:20161759;
    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:NP628518.RAATMENqdj1aQDaz4rZPeQ2_xmPxC6ZQOZE_kFqHOt6qk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:19+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" .
}