@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP685476.RAg09qsvRw6vQAPxC-mtvKRp0iLDsHPgmJk5yptUbjmCQ> .
@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:NP685476.RAg09qsvRw6vQAPxC-mtvKRp0iLDsHPgmJk5yptUbjmCQ130_head {
  this: np:hasAssertion dgn-np:NP685476.RAg09qsvRw6vQAPxC-mtvKRp0iLDsHPgmJk5yptUbjmCQ130_assertion ;
    np:hasProvenance dgn-np:NP685476.RAg09qsvRw6vQAPxC-mtvKRp0iLDsHPgmJk5yptUbjmCQ130_provenance ;
    np:hasPublicationInfo dgn-np:NP685476.RAg09qsvRw6vQAPxC-mtvKRp0iLDsHPgmJk5yptUbjmCQ130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP685476.RAg09qsvRw6vQAPxC-mtvKRp0iLDsHPgmJk5yptUbjmCQ130_assertion a np:Assertion .
  dgn-np:NP685476.RAg09qsvRw6vQAPxC-mtvKRp0iLDsHPgmJk5yptUbjmCQ130_provenance a np:Provenance .
  dgn-np:NP685476.RAg09qsvRw6vQAPxC-mtvKRp0iLDsHPgmJk5yptUbjmCQ130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP685476.RAg09qsvRw6vQAPxC-mtvKRp0iLDsHPgmJk5yptUbjmCQ130_assertion {
  miriam-gene:3342 a ncit:C16612 .
  lld:C0030521 a ncit:C7057 .
  dgn-gda:DGN665fbd597e2dfd2ea5c14e29c35e6b0e sio:SIO_000628 miriam-gene:3342 , lld:C0030521 ;
    a sio:SIO_001121 .
}
dgn-np:NP685476.RAg09qsvRw6vQAPxC-mtvKRp0iLDsHPgmJk5yptUbjmCQ130_provenance {
  dgn-np:NP685476.RAg09qsvRw6vQAPxC-mtvKRp0iLDsHPgmJk5yptUbjmCQ130_assertion dcterms:description "[For this purpose, nine parathyroid tumors with established CDC73 gene inactivating mutations (three carcinomas, one atypical adenoma and five adenomas) were analyzed for copy number alterations and loss of heterozygosity using array-comparative genomic hybridization (a-CGH) and single nucleotide polymorphism (SNP) microarrays, 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:23029479 ;
    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:NP685476.RAg09qsvRw6vQAPxC-mtvKRp0iLDsHPgmJk5yptUbjmCQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:56+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" .
}