@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP271502.RAJuOZvT_olN9W502DIHGi6bArGI97pZcP64CNUekAY9Y> .
@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:NP271502.RAJuOZvT_olN9W502DIHGi6bArGI97pZcP64CNUekAY9Y130_head {
  this: np:hasAssertion dgn-np:NP271502.RAJuOZvT_olN9W502DIHGi6bArGI97pZcP64CNUekAY9Y130_assertion;
    np:hasProvenance dgn-np:NP271502.RAJuOZvT_olN9W502DIHGi6bArGI97pZcP64CNUekAY9Y130_provenance;
    np:hasPublicationInfo dgn-np:NP271502.RAJuOZvT_olN9W502DIHGi6bArGI97pZcP64CNUekAY9Y130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP271502.RAJuOZvT_olN9W502DIHGi6bArGI97pZcP64CNUekAY9Y130_assertion a np:Assertion .
  
  dgn-np:NP271502.RAJuOZvT_olN9W502DIHGi6bArGI97pZcP64CNUekAY9Y130_provenance a np:Provenance .
  
  dgn-np:NP271502.RAJuOZvT_olN9W502DIHGi6bArGI97pZcP64CNUekAY9Y130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP271502.RAJuOZvT_olN9W502DIHGi6bArGI97pZcP64CNUekAY9Y130_assertion {
  miriam-gene:1029 a ncit:C16612 .
  
  lld:C0013403 a ncit:C7057 .
  
  dgn-gda:DGNebf63661df5844d1261d87ac791079f5 sio:SIO_000628 miriam-gene:1029, lld:C0013403;
    a sio:SIO_001121 .
}

dgn-np:NP271502.RAJuOZvT_olN9W502DIHGi6bArGI97pZcP64CNUekAY9Y130_provenance {
  dgn-np:NP271502.RAJuOZvT_olN9W502DIHGi6bArGI97pZcP64CNUekAY9Y130_assertion dcterms:description
      "[We have correlated the atypical mole syndrome phenotype and gene carrier status in five families with germline CDKN2A mutations and shown that family members with the atypical mole syndrome were three times more likely to be mutant gene carriers than their relatives who did not have the atypical mole syndrome (odds ratio 3.4; confidence interval 1.0-11.]. 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:10620111;
    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:NP271502.RAJuOZvT_olN9W502DIHGi6bArGI97pZcP64CNUekAY9Y130_publicationInfo {
  this: dcterms:created "2016-05-13T12:43:49+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" .
}