@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP831635.RAEFRdxZTCb6X_8OPbbS-afUY2cxQ5gcv6dQkdHVNt1oY> .
@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:NP831635.RAEFRdxZTCb6X_8OPbbS-afUY2cxQ5gcv6dQkdHVNt1oY130_head {
  this: np:hasAssertion dgn-np:NP831635.RAEFRdxZTCb6X_8OPbbS-afUY2cxQ5gcv6dQkdHVNt1oY130_assertion;
    np:hasProvenance dgn-np:NP831635.RAEFRdxZTCb6X_8OPbbS-afUY2cxQ5gcv6dQkdHVNt1oY130_provenance;
    np:hasPublicationInfo dgn-np:NP831635.RAEFRdxZTCb6X_8OPbbS-afUY2cxQ5gcv6dQkdHVNt1oY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP831635.RAEFRdxZTCb6X_8OPbbS-afUY2cxQ5gcv6dQkdHVNt1oY130_assertion a np:Assertion .
  
  dgn-np:NP831635.RAEFRdxZTCb6X_8OPbbS-afUY2cxQ5gcv6dQkdHVNt1oY130_provenance a np:Provenance .
  
  dgn-np:NP831635.RAEFRdxZTCb6X_8OPbbS-afUY2cxQ5gcv6dQkdHVNt1oY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP831635.RAEFRdxZTCb6X_8OPbbS-afUY2cxQ5gcv6dQkdHVNt1oY130_assertion {
  miriam-gene:3342 a ncit:C16612 .
  
  lld:C0030521 a ncit:C7057 .
  
  dgn-gda:DGNfe6b2c4ae1337e930936b3166fd7598c sio:SIO_000628 miriam-gene:3342, lld:C0030521;
    a sio:SIO_001121 .
}

dgn-np:NP831635.RAEFRdxZTCb6X_8OPbbS-afUY2cxQ5gcv6dQkdHVNt1oY130_provenance {
  dgn-np:NP831635.RAEFRdxZTCb6X_8OPbbS-afUY2cxQ5gcv6dQkdHVNt1oY130_assertion dcterms:description
      "[Most of the information about the genetic composition of parathyroid tumors has been obtained by comparative genomic hybridization (CGH) and loss of heterozygosity (LOH) studies, whereas only few conventional cytogenetic investigation results are available.]. 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:17455879;
    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:NP831635.RAEFRdxZTCb6X_8OPbbS-afUY2cxQ5gcv6dQkdHVNt1oY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:29+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" .
}