@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP551616.RA7OEkWZBYLsXWhGMyfFR7CAWsKzw8KeDZ1YPgHmOn3mI> .
@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/v4.0.0/void/> .

dgn-np:NP551616.RA7OEkWZBYLsXWhGMyfFR7CAWsKzw8KeDZ1YPgHmOn3mI130_head {
  this: np:hasAssertion dgn-np:NP551616.RA7OEkWZBYLsXWhGMyfFR7CAWsKzw8KeDZ1YPgHmOn3mI130_assertion;
    np:hasProvenance dgn-np:NP551616.RA7OEkWZBYLsXWhGMyfFR7CAWsKzw8KeDZ1YPgHmOn3mI130_provenance;
    np:hasPublicationInfo dgn-np:NP551616.RA7OEkWZBYLsXWhGMyfFR7CAWsKzw8KeDZ1YPgHmOn3mI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP551616.RA7OEkWZBYLsXWhGMyfFR7CAWsKzw8KeDZ1YPgHmOn3mI130_assertion a np:Assertion .
  
  dgn-np:NP551616.RA7OEkWZBYLsXWhGMyfFR7CAWsKzw8KeDZ1YPgHmOn3mI130_provenance a np:Provenance .
  
  dgn-np:NP551616.RA7OEkWZBYLsXWhGMyfFR7CAWsKzw8KeDZ1YPgHmOn3mI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP551616.RA7OEkWZBYLsXWhGMyfFR7CAWsKzw8KeDZ1YPgHmOn3mI130_assertion {
  miriam-gene:5979 a ncit:C16612 .
  
  lld:C0031511 a ncit:C7057 .
  
  dgn-gda:DGN6fab8d2bb1b2e6b839652c7d40774568 sio:SIO_000628 miriam-gene:5979, lld:C0031511;
    a sio:SIO_001121 .
}

dgn-np:NP551616.RA7OEkWZBYLsXWhGMyfFR7CAWsKzw8KeDZ1YPgHmOn3mI130_provenance {
  dgn-np:NP551616.RA7OEkWZBYLsXWhGMyfFR7CAWsKzw8KeDZ1YPgHmOn3mI130_assertion dcterms:description
      "[Germline VHL mutations may be detected in 5-11% of all phaeochromocytoma cases and mutation analysis of VHL and other phaeochromocytoma susceptibility genes (SDHB, SDHD and RET) should be performed in all cases of familial, multiple or early onset phaeochromocytomas, and considered in other cases.]. 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:16728571;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP551616.RA7OEkWZBYLsXWhGMyfFR7CAWsKzw8KeDZ1YPgHmOn3mI130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:55+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}