@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP173139.RAcKBJM2p6Qv9iOwyuehiGB31ocmzU-5MYDtEyibO1_a4> .
@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:NP173139.RAcKBJM2p6Qv9iOwyuehiGB31ocmzU-5MYDtEyibO1_a4130_head {
  this: np:hasAssertion dgn-np:NP173139.RAcKBJM2p6Qv9iOwyuehiGB31ocmzU-5MYDtEyibO1_a4130_assertion;
    np:hasProvenance dgn-np:NP173139.RAcKBJM2p6Qv9iOwyuehiGB31ocmzU-5MYDtEyibO1_a4130_provenance;
    np:hasPublicationInfo dgn-np:NP173139.RAcKBJM2p6Qv9iOwyuehiGB31ocmzU-5MYDtEyibO1_a4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP173139.RAcKBJM2p6Qv9iOwyuehiGB31ocmzU-5MYDtEyibO1_a4130_assertion a np:Assertion .
  
  dgn-np:NP173139.RAcKBJM2p6Qv9iOwyuehiGB31ocmzU-5MYDtEyibO1_a4130_provenance a np:Provenance .
  
  dgn-np:NP173139.RAcKBJM2p6Qv9iOwyuehiGB31ocmzU-5MYDtEyibO1_a4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP173139.RAcKBJM2p6Qv9iOwyuehiGB31ocmzU-5MYDtEyibO1_a4130_assertion {
  miriam-gene:83478 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGN199913b9da3cf174e09b7f629fbd840d sio:SIO_000628 miriam-gene:83478, lld:C0006826;
    a sio:SIO_001121 .
}

dgn-np:NP173139.RAcKBJM2p6Qv9iOwyuehiGB31ocmzU-5MYDtEyibO1_a4130_provenance {
  dgn-np:NP173139.RAcKBJM2p6Qv9iOwyuehiGB31ocmzU-5MYDtEyibO1_a4130_assertion dcterms:description
      "[While p73 is rarely mutated in spontaneous tumors, the expression status of p73 is linked to the sensitivity of tumor cells to chemotherapy and prognosis for many types of human 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:21852228;
    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:NP173139.RAcKBJM2p6Qv9iOwyuehiGB31ocmzU-5MYDtEyibO1_a4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:33+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" .
}