@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP372778.RAKb9K7uOU1oE9MThFy3a7Wc0LfXZ6jHrmAlYneIWKFS8> .
@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:NP372778.RAKb9K7uOU1oE9MThFy3a7Wc0LfXZ6jHrmAlYneIWKFS8130_head {
  this: np:hasAssertion dgn-np:NP372778.RAKb9K7uOU1oE9MThFy3a7Wc0LfXZ6jHrmAlYneIWKFS8130_assertion;
    np:hasProvenance dgn-np:NP372778.RAKb9K7uOU1oE9MThFy3a7Wc0LfXZ6jHrmAlYneIWKFS8130_provenance;
    np:hasPublicationInfo dgn-np:NP372778.RAKb9K7uOU1oE9MThFy3a7Wc0LfXZ6jHrmAlYneIWKFS8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP372778.RAKb9K7uOU1oE9MThFy3a7Wc0LfXZ6jHrmAlYneIWKFS8130_assertion a np:Assertion .
  
  dgn-np:NP372778.RAKb9K7uOU1oE9MThFy3a7Wc0LfXZ6jHrmAlYneIWKFS8130_provenance a np:Provenance .
  
  dgn-np:NP372778.RAKb9K7uOU1oE9MThFy3a7Wc0LfXZ6jHrmAlYneIWKFS8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP372778.RAKb9K7uOU1oE9MThFy3a7Wc0LfXZ6jHrmAlYneIWKFS8130_assertion {
  miriam-gene:11076 a ncit:C16612 .
  
  lld:C0007134 a ncit:C7057 .
  
  dgn-gda:DGNb3e62969ca4f470c292c6ef2f9fa9372 sio:SIO_000628 miriam-gene:11076, lld:C0007134;
    a sio:SIO_001121 .
}

dgn-np:NP372778.RAKb9K7uOU1oE9MThFy3a7Wc0LfXZ6jHrmAlYneIWKFS8130_provenance {
  dgn-np:NP372778.RAKb9K7uOU1oE9MThFy3a7Wc0LfXZ6jHrmAlYneIWKFS8130_assertion dcterms:description
      "[The majority of these markers clustered in three regions that have been suggested to be involved in the development of RCC, namely the p25 region, where the von Hippel Lindau (VHL) gene is located; the p21 region, which has been identified as a common region of overlap (SRO) of heterozygous deletions; and the p14 region, which is the location of the constitutional t(3;8) breakpoint occurring in an RCC family.]. 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:8824727;
    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:NP372778.RAKb9K7uOU1oE9MThFy3a7Wc0LfXZ6jHrmAlYneIWKFS8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:38+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" .
}