@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP402596.RA7zBWmFWZ__2YFAMpx8zQmCggW8pMDUJ5HilE9pVc0DA> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP402596.RA7zBWmFWZ__2YFAMpx8zQmCggW8pMDUJ5HilE9pVc0DA130_head {
  this: np:hasAssertion dgn-np:NP402596.RA7zBWmFWZ__2YFAMpx8zQmCggW8pMDUJ5HilE9pVc0DA130_assertion;
    np:hasProvenance dgn-np:NP402596.RA7zBWmFWZ__2YFAMpx8zQmCggW8pMDUJ5HilE9pVc0DA130_provenance;
    np:hasPublicationInfo dgn-np:NP402596.RA7zBWmFWZ__2YFAMpx8zQmCggW8pMDUJ5HilE9pVc0DA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP402596.RA7zBWmFWZ__2YFAMpx8zQmCggW8pMDUJ5HilE9pVc0DA130_assertion a np:Assertion .
  
  dgn-np:NP402596.RA7zBWmFWZ__2YFAMpx8zQmCggW8pMDUJ5HilE9pVc0DA130_provenance a np:Provenance .
  
  dgn-np:NP402596.RA7zBWmFWZ__2YFAMpx8zQmCggW8pMDUJ5HilE9pVc0DA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP402596.RA7zBWmFWZ__2YFAMpx8zQmCggW8pMDUJ5HilE9pVc0DA130_assertion {
  miriam-gene:2271 a ncit:C16612 .
  
  lld:C1378703 a ncit:C7057 .
  
  dgn-gda:DGN6161f43330d7084c8a246b8d0d43be39 sio:SIO_000628 miriam-gene:2271, lld:C1378703;
    a sio:SIO_001121 .
}

dgn-np:NP402596.RA7zBWmFWZ__2YFAMpx8zQmCggW8pMDUJ5HilE9pVc0DA130_provenance {
  dgn-np:NP402596.RA7zBWmFWZ__2YFAMpx8zQmCggW8pMDUJ5HilE9pVc0DA130_assertion dcterms:description
      "[Hereditary leiomyomatosis and renal cell carcinoma (HLRCC) syndrome is an autosomal dominant disorder in which germline mutations of fumarate hydratase (FH) gene confer an increased risk of cutaneous and uterine leiomyomas and renal cancer.]. 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:24441663;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP402596.RA7zBWmFWZ__2YFAMpx8zQmCggW8pMDUJ5HilE9pVc0DA130_publicationInfo {
  this: dcterms:created "2015-08-25T14:41:34+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}