@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP358195.RAA9YY3U7o5UZemu5s3Zrub4qGHCmxCJPmqIs-oUazaSI> .
@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 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:NP358195.RAA9YY3U7o5UZemu5s3Zrub4qGHCmxCJPmqIs-oUazaSI130_head {
  this: np:hasAssertion dgn-np:NP358195.RAA9YY3U7o5UZemu5s3Zrub4qGHCmxCJPmqIs-oUazaSI130_assertion;
    np:hasProvenance dgn-np:NP358195.RAA9YY3U7o5UZemu5s3Zrub4qGHCmxCJPmqIs-oUazaSI130_provenance;
    np:hasPublicationInfo dgn-np:NP358195.RAA9YY3U7o5UZemu5s3Zrub4qGHCmxCJPmqIs-oUazaSI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP358195.RAA9YY3U7o5UZemu5s3Zrub4qGHCmxCJPmqIs-oUazaSI130_assertion a np:Assertion .
  
  dgn-np:NP358195.RAA9YY3U7o5UZemu5s3Zrub4qGHCmxCJPmqIs-oUazaSI130_provenance a np:Provenance .
  
  dgn-np:NP358195.RAA9YY3U7o5UZemu5s3Zrub4qGHCmxCJPmqIs-oUazaSI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP358195.RAA9YY3U7o5UZemu5s3Zrub4qGHCmxCJPmqIs-oUazaSI130_assertion {
  miriam-gene:8878 a ncit:C16612 .
  
  lld:C1368019 a ncit:C7057 .
  
  dgn-gda:DGNce413fd24b69b03cdf9aad18f87be14b sio:SIO_000628 miriam-gene:8878, lld:C1368019;
    a sio:SIO_001121 .
}

dgn-np:NP358195.RAA9YY3U7o5UZemu5s3Zrub4qGHCmxCJPmqIs-oUazaSI130_provenance {
  dgn-np:NP358195.RAA9YY3U7o5UZemu5s3Zrub4qGHCmxCJPmqIs-oUazaSI130_assertion dct:description
      "[New insights from the biology of adolescent osteosarcomas, VCP and SQSTM1 mutations now defined in patients with Paget's disease, and emerging evidence that stromal lesions are present in patients with Paget's disease are changing the way we think about the pathogenesis of PDB and the rare complication of pagetic osteosarcomas.]. 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:17229010;
    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:NP358195.RAA9YY3U7o5UZemu5s3Zrub4qGHCmxCJPmqIs-oUazaSI130_publicationInfo {
  this: dct:created "2014-10-02T12:35:30+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}