@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP298028.RA5y6oCEEYq8BWp_F6vHgtkoUcyQk1DGWzZGe0NGeefo4> .
@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:NP298028.RA5y6oCEEYq8BWp_F6vHgtkoUcyQk1DGWzZGe0NGeefo4130_head {
  this: np:hasAssertion dgn-np:NP298028.RA5y6oCEEYq8BWp_F6vHgtkoUcyQk1DGWzZGe0NGeefo4130_assertion;
    np:hasProvenance dgn-np:NP298028.RA5y6oCEEYq8BWp_F6vHgtkoUcyQk1DGWzZGe0NGeefo4130_provenance;
    np:hasPublicationInfo dgn-np:NP298028.RA5y6oCEEYq8BWp_F6vHgtkoUcyQk1DGWzZGe0NGeefo4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP298028.RA5y6oCEEYq8BWp_F6vHgtkoUcyQk1DGWzZGe0NGeefo4130_assertion a np:Assertion .
  
  dgn-np:NP298028.RA5y6oCEEYq8BWp_F6vHgtkoUcyQk1DGWzZGe0NGeefo4130_provenance a np:Provenance .
  
  dgn-np:NP298028.RA5y6oCEEYq8BWp_F6vHgtkoUcyQk1DGWzZGe0NGeefo4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP298028.RA5y6oCEEYq8BWp_F6vHgtkoUcyQk1DGWzZGe0NGeefo4130_assertion {
  miriam-gene:324 a ncit:C16612 .
  
  lld:C0030297 a ncit:C7057 .
  
  dgn-gda:DGN924bb57b8bae304e28c55843863c3851 sio:SIO_000628 miriam-gene:324, lld:C0030297;
    a sio:SIO_001121 .
}

dgn-np:NP298028.RA5y6oCEEYq8BWp_F6vHgtkoUcyQk1DGWzZGe0NGeefo4130_provenance {
  dgn-np:NP298028.RA5y6oCEEYq8BWp_F6vHgtkoUcyQk1DGWzZGe0NGeefo4130_assertion dcterms:description
      "[The presence of normal allelic deletions of the APC gene in bilateral parathyroid tumors and nuclear staining of beta-catenin in the pancreatic tumor in addition to the germline mutations suggests that functional loss of the APC gene played an important role not only in familial adenomatous polyposis but also in the MEN1-related tumors in this case.]. 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:11756777;
    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:NP298028.RA5y6oCEEYq8BWp_F6vHgtkoUcyQk1DGWzZGe0NGeefo4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:49+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" .
}