@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP648521.RAHo2bw4yGcoC3x0qSLfY_ZXRX8CigztpNfwq21v_16Ys> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP648521.RAHo2bw4yGcoC3x0qSLfY_ZXRX8CigztpNfwq21v_16Ys130_head {
  this: np:hasAssertion dgn-np:NP648521.RAHo2bw4yGcoC3x0qSLfY_ZXRX8CigztpNfwq21v_16Ys130_assertion;
    np:hasProvenance dgn-np:NP648521.RAHo2bw4yGcoC3x0qSLfY_ZXRX8CigztpNfwq21v_16Ys130_provenance;
    np:hasPublicationInfo dgn-np:NP648521.RAHo2bw4yGcoC3x0qSLfY_ZXRX8CigztpNfwq21v_16Ys130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP648521.RAHo2bw4yGcoC3x0qSLfY_ZXRX8CigztpNfwq21v_16Ys130_assertion a np:Assertion .
  
  dgn-np:NP648521.RAHo2bw4yGcoC3x0qSLfY_ZXRX8CigztpNfwq21v_16Ys130_provenance a np:Provenance .
  
  dgn-np:NP648521.RAHo2bw4yGcoC3x0qSLfY_ZXRX8CigztpNfwq21v_16Ys130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP648521.RAHo2bw4yGcoC3x0qSLfY_ZXRX8CigztpNfwq21v_16Ys130_assertion {
  miriam-gene:5624 a ncit:C16612 .
  
  lld:C0699790 a ncit:C7057 .
  
  dgn-gda:DGN409f1113e6d92c820da960b47859d38e sio:SIO_000628 miriam-gene:5624, lld:C0699790;
    a sio:SIO_001121 .
}

dgn-np:NP648521.RAHo2bw4yGcoC3x0qSLfY_ZXRX8CigztpNfwq21v_16Ys130_provenance {
  dgn-np:NP648521.RAHo2bw4yGcoC3x0qSLfY_ZXRX8CigztpNfwq21v_16Ys130_assertion dcterms:description
      "[Mutations in APC or CTNNB1 are highly frequent in colon cancer and cause aberrant stabilization of CTNNB1, which activates the transcription of Wnt target genes by binding to chromatin via the TCF/LEF transcription factors.]. 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:24651522;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP648521.RAHo2bw4yGcoC3x0qSLfY_ZXRX8CigztpNfwq21v_16Ys130_publicationInfo {
  this: dcterms:created "2015-08-25T14:44:09+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}