@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP352462.RAU9dbU6e3fRprmVT5magEtktr-swdQ4g3Jav9Msksm_U> .
@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:NP352462.RAU9dbU6e3fRprmVT5magEtktr-swdQ4g3Jav9Msksm_U130_head {
  this: np:hasAssertion dgn-np:NP352462.RAU9dbU6e3fRprmVT5magEtktr-swdQ4g3Jav9Msksm_U130_assertion;
    np:hasProvenance dgn-np:NP352462.RAU9dbU6e3fRprmVT5magEtktr-swdQ4g3Jav9Msksm_U130_provenance;
    np:hasPublicationInfo dgn-np:NP352462.RAU9dbU6e3fRprmVT5magEtktr-swdQ4g3Jav9Msksm_U130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP352462.RAU9dbU6e3fRprmVT5magEtktr-swdQ4g3Jav9Msksm_U130_assertion a np:Assertion .
  
  dgn-np:NP352462.RAU9dbU6e3fRprmVT5magEtktr-swdQ4g3Jav9Msksm_U130_provenance a np:Provenance .
  
  dgn-np:NP352462.RAU9dbU6e3fRprmVT5magEtktr-swdQ4g3Jav9Msksm_U130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP352462.RAU9dbU6e3fRprmVT5magEtktr-swdQ4g3Jav9Msksm_U130_assertion {
  miriam-gene:7869 a ncit:C16612 .
  
  lld:C0242379 a ncit:C7057 .
  
  dgn-gda:DGN99d4e93fc6f148f0db09b3a34619d691 sio:SIO_000628 miriam-gene:7869, lld:C0242379;
    a sio:SIO_001121 .
}

dgn-np:NP352462.RAU9dbU6e3fRprmVT5magEtktr-swdQ4g3Jav9Msksm_U130_provenance {
  dgn-np:NP352462.RAU9dbU6e3fRprmVT5magEtktr-swdQ4g3Jav9Msksm_U130_assertion dcterms:description
      "[Non-small cell lung cancer frequently shows loss of heterozygosity of the chromosome 3p21.3 region and several genes such as RASSF1A, BLU, and SEMA3B have been identified as candidate tumor suppressor genes at this region since their downregulation and hypermethylation at their promoter regions were frequently detected in lung cancer.]. 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:15922865;
    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:NP352462.RAU9dbU6e3fRprmVT5magEtktr-swdQ4g3Jav9Msksm_U130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:27+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" .
}