@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP205835.RAbmepN9A2QUiDN5oGKhEEaQz17Xh8s9W-MClf3TqIUuo> .
@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:NP205835.RAbmepN9A2QUiDN5oGKhEEaQz17Xh8s9W-MClf3TqIUuo130_head {
  this: np:hasAssertion dgn-np:NP205835.RAbmepN9A2QUiDN5oGKhEEaQz17Xh8s9W-MClf3TqIUuo130_assertion ;
    np:hasProvenance dgn-np:NP205835.RAbmepN9A2QUiDN5oGKhEEaQz17Xh8s9W-MClf3TqIUuo130_provenance ;
    np:hasPublicationInfo dgn-np:NP205835.RAbmepN9A2QUiDN5oGKhEEaQz17Xh8s9W-MClf3TqIUuo130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP205835.RAbmepN9A2QUiDN5oGKhEEaQz17Xh8s9W-MClf3TqIUuo130_assertion a np:Assertion .
  dgn-np:NP205835.RAbmepN9A2QUiDN5oGKhEEaQz17Xh8s9W-MClf3TqIUuo130_provenance a np:Provenance .
  dgn-np:NP205835.RAbmepN9A2QUiDN5oGKhEEaQz17Xh8s9W-MClf3TqIUuo130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP205835.RAbmepN9A2QUiDN5oGKhEEaQz17Xh8s9W-MClf3TqIUuo130_assertion {
  miriam-gene:1029 a ncit:C16612 .
  lld:C0342494 a ncit:C7057 .
  dgn-gda:DGN9fe93413dcbe66144a332f316580fc27 sio:SIO_000628 miriam-gene:1029 , lld:C0342494 ;
    a sio:SIO_001121 .
}
dgn-np:NP205835.RAbmepN9A2QUiDN5oGKhEEaQz17Xh8s9W-MClf3TqIUuo130_provenance {
  dgn-np:NP205835.RAbmepN9A2QUiDN5oGKhEEaQz17Xh8s9W-MClf3TqIUuo130_assertion dcterms:description "[Differentiation between benign and malignant tumors of the adrenal cortex was attempted by microdissection of nine cases of adrenal cortical hyperplasia, 10 cortical adenomas, and 18 adrenal cortical carcinomas with subsequent polymerase chain reaction (PCR) amplification for loss of heterozygosity (LOH) of five microsatellites of putative tumor suppressor gene loci: p53 gene (17p), the neuroblastoma candidate gene (1p), the p16 gene (9p), the von Hippel Lindau gene (3p), and the retinoblastoma gene (13q).]. 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:9596277 ;
    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:NP205835.RAbmepN9A2QUiDN5oGKhEEaQz17Xh8s9W-MClf3TqIUuo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:53+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" .
}