@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1255062.RAH1beAoJX4Lc83pWl5Qi65dEWFQvx2nySPC5MnjltbCA> .
@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:NP1255062.RAH1beAoJX4Lc83pWl5Qi65dEWFQvx2nySPC5MnjltbCA130_head {
  this: np:hasAssertion dgn-np:NP1255062.RAH1beAoJX4Lc83pWl5Qi65dEWFQvx2nySPC5MnjltbCA130_assertion;
    np:hasProvenance dgn-np:NP1255062.RAH1beAoJX4Lc83pWl5Qi65dEWFQvx2nySPC5MnjltbCA130_provenance;
    np:hasPublicationInfo dgn-np:NP1255062.RAH1beAoJX4Lc83pWl5Qi65dEWFQvx2nySPC5MnjltbCA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1255062.RAH1beAoJX4Lc83pWl5Qi65dEWFQvx2nySPC5MnjltbCA130_assertion a np:Assertion .
  
  dgn-np:NP1255062.RAH1beAoJX4Lc83pWl5Qi65dEWFQvx2nySPC5MnjltbCA130_provenance a np:Provenance .
  
  dgn-np:NP1255062.RAH1beAoJX4Lc83pWl5Qi65dEWFQvx2nySPC5MnjltbCA130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1255062.RAH1beAoJX4Lc83pWl5Qi65dEWFQvx2nySPC5MnjltbCA130_assertion {
  miriam-gene:54894 a ncit:C16612 .
  
  lld:C0009402 a ncit:C7057 .
  
  dgn-gda:DGN30f62cc6bc74fdc4e435802e1a5bb08f sio:SIO_000628 miriam-gene:54894, lld:C0009402;
    a sio:SIO_001121 .
}

dgn-np:NP1255062.RAH1beAoJX4Lc83pWl5Qi65dEWFQvx2nySPC5MnjltbCA130_provenance {
  dgn-np:NP1255062.RAH1beAoJX4Lc83pWl5Qi65dEWFQvx2nySPC5MnjltbCA130_assertion dcterms:description
      "[A new study suggests that RNF43 is one of the most commonly mutated genes in endometrial and colorectal cancers and may help identify patients who could potentially benefit from drugs that target the Wnt signaling pathway.]. 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:25583782;
    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:NP1255062.RAH1beAoJX4Lc83pWl5Qi65dEWFQvx2nySPC5MnjltbCA130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:15+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" .
}