@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP690325.RAGBloZsPDvmCLGNz_6XUorKX9NYDdkKGscTir08luPEI> .
@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:NP690325.RAGBloZsPDvmCLGNz_6XUorKX9NYDdkKGscTir08luPEI130_head {
  this: np:hasAssertion dgn-np:NP690325.RAGBloZsPDvmCLGNz_6XUorKX9NYDdkKGscTir08luPEI130_assertion;
    np:hasProvenance dgn-np:NP690325.RAGBloZsPDvmCLGNz_6XUorKX9NYDdkKGscTir08luPEI130_provenance;
    np:hasPublicationInfo dgn-np:NP690325.RAGBloZsPDvmCLGNz_6XUorKX9NYDdkKGscTir08luPEI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP690325.RAGBloZsPDvmCLGNz_6XUorKX9NYDdkKGscTir08luPEI130_assertion a np:Assertion .
  
  dgn-np:NP690325.RAGBloZsPDvmCLGNz_6XUorKX9NYDdkKGscTir08luPEI130_provenance a np:Provenance .
  
  dgn-np:NP690325.RAGBloZsPDvmCLGNz_6XUorKX9NYDdkKGscTir08luPEI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP690325.RAGBloZsPDvmCLGNz_6XUorKX9NYDdkKGscTir08luPEI130_assertion {
  miriam-gene:50947 a ncit:C16612 .
  
  lld:C0009402 a ncit:C7057 .
  
  dgn-gda:DGN8820844e531218658b017d4fa88ef20f sio:SIO_000628 miriam-gene:50947, lld:C0009402;
    a sio:SIO_001121 .
}

dgn-np:NP690325.RAGBloZsPDvmCLGNz_6XUorKX9NYDdkKGscTir08luPEI130_provenance {
  dgn-np:NP690325.RAGBloZsPDvmCLGNz_6XUorKX9NYDdkKGscTir08luPEI130_assertion dcterms:description
      "[The studies investigated whether individuals with familial colorectal cancer of unknown cause might have unsuspected germline FLCN mutations, looked for somatic FLCN C(8) tract mutations in microsatellite unstable sporadic colorectal cancers, and assessed the risk of colorectal neoplasia and possible genotype-phenotype correlations in BHD patients.]. 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:20522427;
    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:NP690325.RAGBloZsPDvmCLGNz_6XUorKX9NYDdkKGscTir08luPEI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:59+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" .
}