@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP171913.RAVc6bbPDL8xfWwg4-OjnO4pH8v1jioxZfZHLF0_lRQfk> .
@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:NP171913.RAVc6bbPDL8xfWwg4-OjnO4pH8v1jioxZfZHLF0_lRQfk130_head {
  this: np:hasAssertion dgn-np:NP171913.RAVc6bbPDL8xfWwg4-OjnO4pH8v1jioxZfZHLF0_lRQfk130_assertion;
    np:hasProvenance dgn-np:NP171913.RAVc6bbPDL8xfWwg4-OjnO4pH8v1jioxZfZHLF0_lRQfk130_provenance;
    np:hasPublicationInfo dgn-np:NP171913.RAVc6bbPDL8xfWwg4-OjnO4pH8v1jioxZfZHLF0_lRQfk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP171913.RAVc6bbPDL8xfWwg4-OjnO4pH8v1jioxZfZHLF0_lRQfk130_assertion a np:Assertion .
  
  dgn-np:NP171913.RAVc6bbPDL8xfWwg4-OjnO4pH8v1jioxZfZHLF0_lRQfk130_provenance a np:Provenance .
  
  dgn-np:NP171913.RAVc6bbPDL8xfWwg4-OjnO4pH8v1jioxZfZHLF0_lRQfk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP171913.RAVc6bbPDL8xfWwg4-OjnO4pH8v1jioxZfZHLF0_lRQfk130_assertion {
  miriam-gene:324 a ncit:C16612 .
  
  lld:C1527249 a ncit:C7057 .
  
  dgn-gda:DGNf2ddf1297f24aabe2d1e4113811ba4ce sio:SIO_000628 miriam-gene:324, lld:C1527249;
    a sio:SIO_001121 .
}

dgn-np:NP171913.RAVc6bbPDL8xfWwg4-OjnO4pH8v1jioxZfZHLF0_lRQfk130_provenance {
  dgn-np:NP171913.RAVc6bbPDL8xfWwg4-OjnO4pH8v1jioxZfZHLF0_lRQfk130_assertion dcterms:description
      "[Because UEC and CRC share other molecular genetic alterations and histologic features and previous studies of UEC have not reported an analysis of the APC gene, we chose to further elucidate the role of the Wnt pathway in UEC.]. 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:11048799;
    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:NP171913.RAVc6bbPDL8xfWwg4-OjnO4pH8v1jioxZfZHLF0_lRQfk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:33+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" .
}