@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP337385.RAxO6kzzXQLi8ezWfZyoy52hr0XI91UoYrUvapg4kXGek> .
@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:NP337385.RAxO6kzzXQLi8ezWfZyoy52hr0XI91UoYrUvapg4kXGek130_head {
  this: np:hasAssertion dgn-np:NP337385.RAxO6kzzXQLi8ezWfZyoy52hr0XI91UoYrUvapg4kXGek130_assertion;
    np:hasProvenance dgn-np:NP337385.RAxO6kzzXQLi8ezWfZyoy52hr0XI91UoYrUvapg4kXGek130_provenance;
    np:hasPublicationInfo dgn-np:NP337385.RAxO6kzzXQLi8ezWfZyoy52hr0XI91UoYrUvapg4kXGek130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP337385.RAxO6kzzXQLi8ezWfZyoy52hr0XI91UoYrUvapg4kXGek130_assertion a np:Assertion .
  
  dgn-np:NP337385.RAxO6kzzXQLi8ezWfZyoy52hr0XI91UoYrUvapg4kXGek130_provenance a np:Provenance .
  
  dgn-np:NP337385.RAxO6kzzXQLi8ezWfZyoy52hr0XI91UoYrUvapg4kXGek130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP337385.RAxO6kzzXQLi8ezWfZyoy52hr0XI91UoYrUvapg4kXGek130_assertion {
  miriam-gene:8600 a ncit:C16612 .
  
  lld:C0268414 a ncit:C7057 .
  
  dgn-gda:DGN3061c3bc666744707157c77e2d050547 sio:SIO_000628 miriam-gene:8600, lld:C0268414;
    a sio:SIO_001121 .
}

dgn-np:NP337385.RAxO6kzzXQLi8ezWfZyoy52hr0XI91UoYrUvapg4kXGek130_provenance {
  dgn-np:NP337385.RAxO6kzzXQLi8ezWfZyoy52hr0XI91UoYrUvapg4kXGek130_assertion dcterms:description
      "[Whilst no mutations in the RANKL gene have yet been identified in human disease, mutations that result in enhanced RANK signalling through inactivation of OPG or activation of RANK are associated with Juvenile Paget's disease and familial expansile osteolysis, respectively.]. 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:17174136;
    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:NP337385.RAxO6kzzXQLi8ezWfZyoy52hr0XI91UoYrUvapg4kXGek130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:18+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" .
}