@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP339105.RA5K4hARJyrTIdaxdaZQtQSA3bfOZQ3phN_sFOzjTSbqU> .
@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:NP339105.RA5K4hARJyrTIdaxdaZQtQSA3bfOZQ3phN_sFOzjTSbqU130_head {
  this: np:hasAssertion dgn-np:NP339105.RA5K4hARJyrTIdaxdaZQtQSA3bfOZQ3phN_sFOzjTSbqU130_assertion;
    np:hasProvenance dgn-np:NP339105.RA5K4hARJyrTIdaxdaZQtQSA3bfOZQ3phN_sFOzjTSbqU130_provenance;
    np:hasPublicationInfo dgn-np:NP339105.RA5K4hARJyrTIdaxdaZQtQSA3bfOZQ3phN_sFOzjTSbqU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP339105.RA5K4hARJyrTIdaxdaZQtQSA3bfOZQ3phN_sFOzjTSbqU130_assertion a np:Assertion .
  
  dgn-np:NP339105.RA5K4hARJyrTIdaxdaZQtQSA3bfOZQ3phN_sFOzjTSbqU130_provenance a np:Provenance .
  
  dgn-np:NP339105.RA5K4hARJyrTIdaxdaZQtQSA3bfOZQ3phN_sFOzjTSbqU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP339105.RA5K4hARJyrTIdaxdaZQtQSA3bfOZQ3phN_sFOzjTSbqU130_assertion {
  miriam-gene:4089 a ncit:C16612 .
  
  lld:C0007097 a ncit:C7057 .
  
  dgn-gda:DGN8e3994edf1fc0c898242c80c311aa8c0 sio:SIO_000628 miriam-gene:4089, lld:C0007097;
    a sio:SIO_001121 .
}

dgn-np:NP339105.RA5K4hARJyrTIdaxdaZQtQSA3bfOZQ3phN_sFOzjTSbqU130_provenance {
  dgn-np:NP339105.RA5K4hARJyrTIdaxdaZQtQSA3bfOZQ3phN_sFOzjTSbqU130_assertion dcterms:description
      "[Five specific `malignant` events (gain of 8q, 13q, and 20q and loss of 17p and 18q) and aberrant staining for p53 and SMAD4 were all increased in the adenoma fractions of carcinoma cases compared with pure adenomas.]. 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:18245538;
    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:NP339105.RA5K4hARJyrTIdaxdaZQtQSA3bfOZQ3phN_sFOzjTSbqU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:19+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" .
}