@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP269258.RAQpzFvdAt2K2e_frjxmb1wKgIZ0Q0I48I6cDm-_9RU7M> .
@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:NP269258.RAQpzFvdAt2K2e_frjxmb1wKgIZ0Q0I48I6cDm-_9RU7M130_head {
  this: np:hasAssertion dgn-np:NP269258.RAQpzFvdAt2K2e_frjxmb1wKgIZ0Q0I48I6cDm-_9RU7M130_assertion;
    np:hasProvenance dgn-np:NP269258.RAQpzFvdAt2K2e_frjxmb1wKgIZ0Q0I48I6cDm-_9RU7M130_provenance;
    np:hasPublicationInfo dgn-np:NP269258.RAQpzFvdAt2K2e_frjxmb1wKgIZ0Q0I48I6cDm-_9RU7M130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP269258.RAQpzFvdAt2K2e_frjxmb1wKgIZ0Q0I48I6cDm-_9RU7M130_assertion a np:Assertion .
  
  dgn-np:NP269258.RAQpzFvdAt2K2e_frjxmb1wKgIZ0Q0I48I6cDm-_9RU7M130_provenance a np:Provenance .
  
  dgn-np:NP269258.RAQpzFvdAt2K2e_frjxmb1wKgIZ0Q0I48I6cDm-_9RU7M130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP269258.RAQpzFvdAt2K2e_frjxmb1wKgIZ0Q0I48I6cDm-_9RU7M130_assertion {
  miriam-gene:1029 a ncit:C16612 .
  
  lld:C0684249 a ncit:C7057 .
  
  dgn-gda:DGN847aa17a08658e117acf111a6dcfcef6 sio:SIO_000628 miriam-gene:1029, lld:C0684249;
    a sio:SIO_001121 .
}

dgn-np:NP269258.RAQpzFvdAt2K2e_frjxmb1wKgIZ0Q0I48I6cDm-_9RU7M130_provenance {
  dgn-np:NP269258.RAQpzFvdAt2K2e_frjxmb1wKgIZ0Q0I48I6cDm-_9RU7M130_assertion dcterms:description
      "[All of these findings are consistent with loss of Fhit protein expression being as frequent an abnormality in lung cancer pathogenesis as are p53 and p16 protein abnormalities and that such loss occurs independently of the commitment to the metastatic state and of most other molecular abnormalities.]. 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:10735505;
    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:NP269258.RAQpzFvdAt2K2e_frjxmb1wKgIZ0Q0I48I6cDm-_9RU7M130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:30+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" .
}