@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP161348.RADbKDVkprP6jeylChNhFuGg2UwnUDn68ZaoiJ-VJtaII> .
@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:NP161348.RADbKDVkprP6jeylChNhFuGg2UwnUDn68ZaoiJ-VJtaII130_head {
  this: np:hasAssertion dgn-np:NP161348.RADbKDVkprP6jeylChNhFuGg2UwnUDn68ZaoiJ-VJtaII130_assertion;
    np:hasProvenance dgn-np:NP161348.RADbKDVkprP6jeylChNhFuGg2UwnUDn68ZaoiJ-VJtaII130_provenance;
    np:hasPublicationInfo dgn-np:NP161348.RADbKDVkprP6jeylChNhFuGg2UwnUDn68ZaoiJ-VJtaII130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP161348.RADbKDVkprP6jeylChNhFuGg2UwnUDn68ZaoiJ-VJtaII130_assertion a np:Assertion .
  
  dgn-np:NP161348.RADbKDVkprP6jeylChNhFuGg2UwnUDn68ZaoiJ-VJtaII130_provenance a np:Provenance .
  
  dgn-np:NP161348.RADbKDVkprP6jeylChNhFuGg2UwnUDn68ZaoiJ-VJtaII130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP161348.RADbKDVkprP6jeylChNhFuGg2UwnUDn68ZaoiJ-VJtaII130_assertion {
  miriam-gene:6390 a ncit:C16612 .
  
  lld:C1333993 a ncit:C7057 .
  
  dgn-gda:DGN3a0b8efc11df2837ddc0cd21ac3745af sio:SIO_000628 miriam-gene:6390, lld:C1333993;
    a sio:SIO_001121 .
}

dgn-np:NP161348.RADbKDVkprP6jeylChNhFuGg2UwnUDn68ZaoiJ-VJtaII130_provenance {
  dgn-np:NP161348.RADbKDVkprP6jeylChNhFuGg2UwnUDn68ZaoiJ-VJtaII130_assertion dcterms:description
      "[A question confronting clinicians is whether they should screen patients with apparently sporadic pheochromocytomas for unsuspected germline mutations of some or all of the seven genes known to cause hereditary paraganglioma or pheochromocytoma (NF1, VHL, RET, MEN1, SDHD, SDHC, and SDHB).]. 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:16735498;
    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:NP161348.RADbKDVkprP6jeylChNhFuGg2UwnUDn68ZaoiJ-VJtaII130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:27+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" .
}