@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1286300.RAxEl1W8vVPiid4_UzKI9RMxEc9O4c7krL50VBgJxlkn4> .
@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/v4.0.0/void/> .

dgn-np:NP1286300.RAxEl1W8vVPiid4_UzKI9RMxEc9O4c7krL50VBgJxlkn4130_head {
  this: np:hasAssertion dgn-np:NP1286300.RAxEl1W8vVPiid4_UzKI9RMxEc9O4c7krL50VBgJxlkn4130_assertion;
    np:hasProvenance dgn-np:NP1286300.RAxEl1W8vVPiid4_UzKI9RMxEc9O4c7krL50VBgJxlkn4130_provenance;
    np:hasPublicationInfo dgn-np:NP1286300.RAxEl1W8vVPiid4_UzKI9RMxEc9O4c7krL50VBgJxlkn4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1286300.RAxEl1W8vVPiid4_UzKI9RMxEc9O4c7krL50VBgJxlkn4130_assertion a np:Assertion .
  
  dgn-np:NP1286300.RAxEl1W8vVPiid4_UzKI9RMxEc9O4c7krL50VBgJxlkn4130_provenance a np:Provenance .
  
  dgn-np:NP1286300.RAxEl1W8vVPiid4_UzKI9RMxEc9O4c7krL50VBgJxlkn4130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1286300.RAxEl1W8vVPiid4_UzKI9RMxEc9O4c7krL50VBgJxlkn4130_assertion {
  miriam-gene:6425 a ncit:C16612 .
  
  lld:C2239176 a ncit:C7057 .
  
  dgn-gda:DGN766c05a11a889420d1e52712b22e5f65 sio:SIO_000628 miriam-gene:6425, lld:C2239176;
    a sio:SIO_001121 .
}

dgn-np:NP1286300.RAxEl1W8vVPiid4_UzKI9RMxEc9O4c7krL50VBgJxlkn4130_provenance {
  dgn-np:NP1286300.RAxEl1W8vVPiid4_UzKI9RMxEc9O4c7krL50VBgJxlkn4130_assertion dcterms:description
      "[By using methylation sensitive restriction enzyme-quantitative PCR, hypermethylation of APC was detected in HCC with different risk factors, whereas SFRP1 and SFRP5 were not hypermethylated in any of the HCC etiologies, which indicates that the mutation of APC and AXIN1, together with the methylation of APC could take part in the overactivation of Wnt signaling.]. 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:26034368;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1286300.RAxEl1W8vVPiid4_UzKI9RMxEc9O4c7krL50VBgJxlkn4130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:29+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}