@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP426542.RAr2Vi1mIrvD-rHAUK2_BtSgFuQ8wpCyvgLKbzG5nI4yc> .
@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:NP426542.RAr2Vi1mIrvD-rHAUK2_BtSgFuQ8wpCyvgLKbzG5nI4yc130_head {
  this: np:hasAssertion dgn-np:NP426542.RAr2Vi1mIrvD-rHAUK2_BtSgFuQ8wpCyvgLKbzG5nI4yc130_assertion;
    np:hasProvenance dgn-np:NP426542.RAr2Vi1mIrvD-rHAUK2_BtSgFuQ8wpCyvgLKbzG5nI4yc130_provenance;
    np:hasPublicationInfo dgn-np:NP426542.RAr2Vi1mIrvD-rHAUK2_BtSgFuQ8wpCyvgLKbzG5nI4yc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP426542.RAr2Vi1mIrvD-rHAUK2_BtSgFuQ8wpCyvgLKbzG5nI4yc130_assertion a np:Assertion .
  
  dgn-np:NP426542.RAr2Vi1mIrvD-rHAUK2_BtSgFuQ8wpCyvgLKbzG5nI4yc130_provenance a np:Provenance .
  
  dgn-np:NP426542.RAr2Vi1mIrvD-rHAUK2_BtSgFuQ8wpCyvgLKbzG5nI4yc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP426542.RAr2Vi1mIrvD-rHAUK2_BtSgFuQ8wpCyvgLKbzG5nI4yc130_assertion {
  miriam-gene:10297 a ncit:C16612 .
  
  lld:C0033036 a ncit:C7057 .
  
  dgn-gda:DGN11ac8059df208a800421b6802e548600 sio:SIO_000628 miriam-gene:10297, lld:C0033036;
    a sio:SIO_001121 .
}

dgn-np:NP426542.RAr2Vi1mIrvD-rHAUK2_BtSgFuQ8wpCyvgLKbzG5nI4yc130_provenance {
  dgn-np:NP426542.RAr2Vi1mIrvD-rHAUK2_BtSgFuQ8wpCyvgLKbzG5nI4yc130_assertion dcterms:description
      "[Our data suggest that the functional complementation of APCL by APC constitutes a substantial facet of tumour development, because the truncating mutations of APC in colorectal tumours from familial adenomatous polyposis (FAP) patients are almost always selected for the retention of at least one 15R.]. 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:23840886;
    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:NP426542.RAr2Vi1mIrvD-rHAUK2_BtSgFuQ8wpCyvgLKbzG5nI4yc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:13+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" .
}