@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP497280.RAPClQb3HJg7e-Vum9L-_hXfxiLjj9K00I3ST-PWHbSpM> .
@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/v4.0.0/void/> .

dgn-np:NP497280.RAPClQb3HJg7e-Vum9L-_hXfxiLjj9K00I3ST-PWHbSpM130_head {
  this: np:hasAssertion dgn-np:NP497280.RAPClQb3HJg7e-Vum9L-_hXfxiLjj9K00I3ST-PWHbSpM130_assertion;
    np:hasProvenance dgn-np:NP497280.RAPClQb3HJg7e-Vum9L-_hXfxiLjj9K00I3ST-PWHbSpM130_provenance;
    np:hasPublicationInfo dgn-np:NP497280.RAPClQb3HJg7e-Vum9L-_hXfxiLjj9K00I3ST-PWHbSpM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP497280.RAPClQb3HJg7e-Vum9L-_hXfxiLjj9K00I3ST-PWHbSpM130_assertion a np:Assertion .
  
  dgn-np:NP497280.RAPClQb3HJg7e-Vum9L-_hXfxiLjj9K00I3ST-PWHbSpM130_provenance a np:Provenance .
  
  dgn-np:NP497280.RAPClQb3HJg7e-Vum9L-_hXfxiLjj9K00I3ST-PWHbSpM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP497280.RAPClQb3HJg7e-Vum9L-_hXfxiLjj9K00I3ST-PWHbSpM130_assertion {
  miriam-gene:1019 a ncit:C16612 .
  
  lld:C0025202 a ncit:C7057 .
  
  dgn-gda:DGNa4c5ed2b801098a5afb2350815a8f5de sio:SIO_000628 miriam-gene:1019, lld:C0025202;
    a sio:SIO_001121 .
}

dgn-np:NP497280.RAPClQb3HJg7e-Vum9L-_hXfxiLjj9K00I3ST-PWHbSpM130_provenance {
  dgn-np:NP497280.RAPClQb3HJg7e-Vum9L-_hXfxiLjj9K00I3ST-PWHbSpM130_assertion dcterms:description
      "[To gain insight into the molecular mechanisms involved in the inherited predisposition to melanoma and associated neural system tumours, 42 Jewish, mainly Ashkenazi, melanoma families with or without neural system tumours were genotyped for germline point mutations and genomic deletions at the CDKN2A/ARF and CDK4 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:15928671;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP497280.RAPClQb3HJg7e-Vum9L-_hXfxiLjj9K00I3ST-PWHbSpM130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:30+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}