@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP674633.RAOUqbsiefKos-RnTllKMQp4_RsBV3tLpM7vX0o1nZmEo> .
@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:NP674633.RAOUqbsiefKos-RnTllKMQp4_RsBV3tLpM7vX0o1nZmEo130_head {
  this: np:hasAssertion dgn-np:NP674633.RAOUqbsiefKos-RnTllKMQp4_RsBV3tLpM7vX0o1nZmEo130_assertion;
    np:hasProvenance dgn-np:NP674633.RAOUqbsiefKos-RnTllKMQp4_RsBV3tLpM7vX0o1nZmEo130_provenance;
    np:hasPublicationInfo dgn-np:NP674633.RAOUqbsiefKos-RnTllKMQp4_RsBV3tLpM7vX0o1nZmEo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP674633.RAOUqbsiefKos-RnTllKMQp4_RsBV3tLpM7vX0o1nZmEo130_assertion a np:Assertion .
  
  dgn-np:NP674633.RAOUqbsiefKos-RnTllKMQp4_RsBV3tLpM7vX0o1nZmEo130_provenance a np:Provenance .
  
  dgn-np:NP674633.RAOUqbsiefKos-RnTllKMQp4_RsBV3tLpM7vX0o1nZmEo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP674633.RAOUqbsiefKos-RnTllKMQp4_RsBV3tLpM7vX0o1nZmEo130_assertion {
  miriam-gene:595 a ncit:C16612 .
  
  lld:C0030521 a ncit:C7057 .
  
  dgn-gda:DGN8eb011b11831d10d6249623db76ec8a5 sio:SIO_000628 miriam-gene:595, lld:C0030521;
    a sio:SIO_001121 .
}

dgn-np:NP674633.RAOUqbsiefKos-RnTllKMQp4_RsBV3tLpM7vX0o1nZmEo130_provenance {
  dgn-np:NP674633.RAOUqbsiefKos-RnTllKMQp4_RsBV3tLpM7vX0o1nZmEo130_assertion dcterms:description
      "[We analyzed a series of parathyroid neoplasms with DNA fluorescent probes to evaluate the diagnostic and prognostic utility of numerical abnormalities of chromosomes 1, 6, 9, 11, 13, 15, 17, and 22 and cyclin D1 and p53 gene loci.]. 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:15105644;
    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:NP674633.RAOUqbsiefKos-RnTllKMQp4_RsBV3tLpM7vX0o1nZmEo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:47+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" .
}