@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP193935.RAXAkYFh3GAtuQT0b7eakZ5LGbM0l5KbeyydGMPawbrZ8> .
@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:NP193935.RAXAkYFh3GAtuQT0b7eakZ5LGbM0l5KbeyydGMPawbrZ8130_head {
  this: np:hasAssertion dgn-np:NP193935.RAXAkYFh3GAtuQT0b7eakZ5LGbM0l5KbeyydGMPawbrZ8130_assertion;
    np:hasProvenance dgn-np:NP193935.RAXAkYFh3GAtuQT0b7eakZ5LGbM0l5KbeyydGMPawbrZ8130_provenance;
    np:hasPublicationInfo dgn-np:NP193935.RAXAkYFh3GAtuQT0b7eakZ5LGbM0l5KbeyydGMPawbrZ8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP193935.RAXAkYFh3GAtuQT0b7eakZ5LGbM0l5KbeyydGMPawbrZ8130_assertion a np:Assertion .
  
  dgn-np:NP193935.RAXAkYFh3GAtuQT0b7eakZ5LGbM0l5KbeyydGMPawbrZ8130_provenance a np:Provenance .
  
  dgn-np:NP193935.RAXAkYFh3GAtuQT0b7eakZ5LGbM0l5KbeyydGMPawbrZ8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP193935.RAXAkYFh3GAtuQT0b7eakZ5LGbM0l5KbeyydGMPawbrZ8130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C0242596 a ncit:C7057 .
  
  dgn-gda:DGNca936c5c752d7035ffa14f119080828a sio:SIO_000628 miriam-gene:7157, lld:C0242596;
    a sio:SIO_001121 .
}

dgn-np:NP193935.RAXAkYFh3GAtuQT0b7eakZ5LGbM0l5KbeyydGMPawbrZ8130_provenance {
  dgn-np:NP193935.RAXAkYFh3GAtuQT0b7eakZ5LGbM0l5KbeyydGMPawbrZ8130_assertion dcterms:description
      "[The feasibility of applying heterogeneous single base genetic changes as tumour specific markers to detect minimal residual disease in PBPC harvests was studied, using the p53 gene and breast cancer as models.]. 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:12032228;
    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:NP193935.RAXAkYFh3GAtuQT0b7eakZ5LGbM0l5KbeyydGMPawbrZ8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:46+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" .
}