@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP622500.RAE7SH13FV0dTyaIog-BAH-spCeluXTc9HF2HxWKCIGd8> .
@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:NP622500.RAE7SH13FV0dTyaIog-BAH-spCeluXTc9HF2HxWKCIGd8130_head {
  this: np:hasAssertion dgn-np:NP622500.RAE7SH13FV0dTyaIog-BAH-spCeluXTc9HF2HxWKCIGd8130_assertion;
    np:hasProvenance dgn-np:NP622500.RAE7SH13FV0dTyaIog-BAH-spCeluXTc9HF2HxWKCIGd8130_provenance;
    np:hasPublicationInfo dgn-np:NP622500.RAE7SH13FV0dTyaIog-BAH-spCeluXTc9HF2HxWKCIGd8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP622500.RAE7SH13FV0dTyaIog-BAH-spCeluXTc9HF2HxWKCIGd8130_assertion a np:Assertion .
  
  dgn-np:NP622500.RAE7SH13FV0dTyaIog-BAH-spCeluXTc9HF2HxWKCIGd8130_provenance a np:Provenance .
  
  dgn-np:NP622500.RAE7SH13FV0dTyaIog-BAH-spCeluXTc9HF2HxWKCIGd8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP622500.RAE7SH13FV0dTyaIog-BAH-spCeluXTc9HF2HxWKCIGd8130_assertion {
  miriam-gene:2271 a ncit:C16612 .
  
  lld:C0022665 a ncit:C7057 .
  
  dgn-gda:DGNaf6bd7e63f250d7d97d58796ac1f5490 sio:SIO_000628 miriam-gene:2271, lld:C0022665;
    a sio:SIO_001121 .
}

dgn-np:NP622500.RAE7SH13FV0dTyaIog-BAH-spCeluXTc9HF2HxWKCIGd8130_provenance {
  dgn-np:NP622500.RAE7SH13FV0dTyaIog-BAH-spCeluXTc9HF2HxWKCIGd8130_assertion dcterms:description
      "[Due to the incomplete penetrance of HLRCC, the authors propose to extend the FH mutation analysis to every patient with PRCCII occurring before 40 years of age or when renal tumour harbours characteristic histologic features, in order to discover previously ignored HLRCC affected families.]. 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:21398687;
    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:NP622500.RAE7SH13FV0dTyaIog-BAH-spCeluXTc9HF2HxWKCIGd8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:16+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" .
}