@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP767131.RA5cNiiExDQLh8phvKmdM8RFM15SwETT3h0_kJYVsJSlc> .
@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:NP767131.RA5cNiiExDQLh8phvKmdM8RFM15SwETT3h0_kJYVsJSlc130_head {
  this: np:hasAssertion dgn-np:NP767131.RA5cNiiExDQLh8phvKmdM8RFM15SwETT3h0_kJYVsJSlc130_assertion;
    np:hasProvenance dgn-np:NP767131.RA5cNiiExDQLh8phvKmdM8RFM15SwETT3h0_kJYVsJSlc130_provenance;
    np:hasPublicationInfo dgn-np:NP767131.RA5cNiiExDQLh8phvKmdM8RFM15SwETT3h0_kJYVsJSlc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP767131.RA5cNiiExDQLh8phvKmdM8RFM15SwETT3h0_kJYVsJSlc130_assertion a np:Assertion .
  
  dgn-np:NP767131.RA5cNiiExDQLh8phvKmdM8RFM15SwETT3h0_kJYVsJSlc130_provenance a np:Provenance .
  
  dgn-np:NP767131.RA5cNiiExDQLh8phvKmdM8RFM15SwETT3h0_kJYVsJSlc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP767131.RA5cNiiExDQLh8phvKmdM8RFM15SwETT3h0_kJYVsJSlc130_assertion {
  miriam-gene:5624 a ncit:C16612 .
  
  lld:C0032927 a ncit:C7057 .
  
  dgn-gda:DGN0036afed67634dbbdba99990880077d5 sio:SIO_000628 miriam-gene:5624, lld:C0032927;
    a sio:SIO_001121 .
}

dgn-np:NP767131.RA5cNiiExDQLh8phvKmdM8RFM15SwETT3h0_kJYVsJSlc130_provenance {
  dgn-np:NP767131.RA5cNiiExDQLh8phvKmdM8RFM15SwETT3h0_kJYVsJSlc130_assertion dcterms:description
      "[Allelic loss at 9p21 (p16 locus), 17p13 (p53) and 5q21(APC) has been frequently described in NSCLC and has also been described in premalignant epithelial lesions of the bronchus and normal bronchial cells.]. 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:17330809;
    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:NP767131.RA5cNiiExDQLh8phvKmdM8RFM15SwETT3h0_kJYVsJSlc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:44+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" .
}