@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP759432.RANFR56wLVtz0KF0kKGpVNOez_FYcDbUMbopuAGTqFlnA> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP759432.RANFR56wLVtz0KF0kKGpVNOez_FYcDbUMbopuAGTqFlnA130_head {
  this: np:hasAssertion dgn-np:NP759432.RANFR56wLVtz0KF0kKGpVNOez_FYcDbUMbopuAGTqFlnA130_assertion;
    np:hasProvenance dgn-np:NP759432.RANFR56wLVtz0KF0kKGpVNOez_FYcDbUMbopuAGTqFlnA130_provenance;
    np:hasPublicationInfo dgn-np:NP759432.RANFR56wLVtz0KF0kKGpVNOez_FYcDbUMbopuAGTqFlnA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP759432.RANFR56wLVtz0KF0kKGpVNOez_FYcDbUMbopuAGTqFlnA130_assertion a np:Assertion .
  
  dgn-np:NP759432.RANFR56wLVtz0KF0kKGpVNOez_FYcDbUMbopuAGTqFlnA130_provenance a np:Provenance .
  
  dgn-np:NP759432.RANFR56wLVtz0KF0kKGpVNOez_FYcDbUMbopuAGTqFlnA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP759432.RANFR56wLVtz0KF0kKGpVNOez_FYcDbUMbopuAGTqFlnA130_assertion {
  miriam-gene:7248 a ncit:C16612 .
  
  lld:C0279680 a ncit:C7057 .
  
  dgn-gda:DGN2372e464ad21cc7ac837507f9a8dacab sio:SIO_000628 miriam-gene:7248, lld:C0279680;
    a sio:SIO_001121 .
}

dgn-np:NP759432.RANFR56wLVtz0KF0kKGpVNOez_FYcDbUMbopuAGTqFlnA130_provenance {
  dgn-np:NP759432.RANFR56wLVtz0KF0kKGpVNOez_FYcDbUMbopuAGTqFlnA130_assertion dcterms:description
      "[While the high frequency of chromosome 9q loss in TCC may reflect destabilization of the chromosome related to hypomethylation of repetitive DNA, the data are compatible with the existence of tumour suppressor genes on this chromosome arm.]. 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:11747331;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP759432.RANFR56wLVtz0KF0kKGpVNOez_FYcDbUMbopuAGTqFlnA130_publicationInfo {
  this: dcterms:created "2015-08-25T14:45:18+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}