@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP491668.RAn6im5fIpKzMMOXNERKKftth91u99b9bPiHRy20l3vHI> .
@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:NP491668.RAn6im5fIpKzMMOXNERKKftth91u99b9bPiHRy20l3vHI130_head {
  this: np:hasAssertion dgn-np:NP491668.RAn6im5fIpKzMMOXNERKKftth91u99b9bPiHRy20l3vHI130_assertion;
    np:hasProvenance dgn-np:NP491668.RAn6im5fIpKzMMOXNERKKftth91u99b9bPiHRy20l3vHI130_provenance;
    np:hasPublicationInfo dgn-np:NP491668.RAn6im5fIpKzMMOXNERKKftth91u99b9bPiHRy20l3vHI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP491668.RAn6im5fIpKzMMOXNERKKftth91u99b9bPiHRy20l3vHI130_assertion a np:Assertion .
  
  dgn-np:NP491668.RAn6im5fIpKzMMOXNERKKftth91u99b9bPiHRy20l3vHI130_provenance a np:Provenance .
  
  dgn-np:NP491668.RAn6im5fIpKzMMOXNERKKftth91u99b9bPiHRy20l3vHI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP491668.RAn6im5fIpKzMMOXNERKKftth91u99b9bPiHRy20l3vHI130_assertion {
  miriam-gene:6390 a ncit:C16612 .
  
  lld:C0027831 a ncit:C7057 .
  
  dgn-gda:DGNd4c30c486ead3ddde2b8f060e444d655 sio:SIO_000628 miriam-gene:6390, lld:C0027831;
    a sio:SIO_001121 .
}

dgn-np:NP491668.RAn6im5fIpKzMMOXNERKKftth91u99b9bPiHRy20l3vHI130_provenance {
  dgn-np:NP491668.RAn6im5fIpKzMMOXNERKKftth91u99b9bPiHRy20l3vHI130_assertion dcterms:description
      "[In the absence of germline mutations in VHL, RET, SDHD, and SDHB, patients with pheochromocytoma, especially with bilateral disease, should be checked thoroughly for clinical lesions suggestive of underlying syndromes such as the cutaneous and ophthalmological features characteristic of NF 1.]. 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:16787982;
    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:NP491668.RAn6im5fIpKzMMOXNERKKftth91u99b9bPiHRy20l3vHI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:53+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" .
}