@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP216551.RAmbKFt2Dy3dYU2ByZUd4GM9v-tAUOhAfhTgvbzXTHVJs> .
@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:NP216551.RAmbKFt2Dy3dYU2ByZUd4GM9v-tAUOhAfhTgvbzXTHVJs130_head {
  this: np:hasAssertion dgn-np:NP216551.RAmbKFt2Dy3dYU2ByZUd4GM9v-tAUOhAfhTgvbzXTHVJs130_assertion;
    np:hasProvenance dgn-np:NP216551.RAmbKFt2Dy3dYU2ByZUd4GM9v-tAUOhAfhTgvbzXTHVJs130_provenance;
    np:hasPublicationInfo dgn-np:NP216551.RAmbKFt2Dy3dYU2ByZUd4GM9v-tAUOhAfhTgvbzXTHVJs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP216551.RAmbKFt2Dy3dYU2ByZUd4GM9v-tAUOhAfhTgvbzXTHVJs130_assertion a np:Assertion .
  
  dgn-np:NP216551.RAmbKFt2Dy3dYU2ByZUd4GM9v-tAUOhAfhTgvbzXTHVJs130_provenance a np:Provenance .
  
  dgn-np:NP216551.RAmbKFt2Dy3dYU2ByZUd4GM9v-tAUOhAfhTgvbzXTHVJs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP216551.RAmbKFt2Dy3dYU2ByZUd4GM9v-tAUOhAfhTgvbzXTHVJs130_assertion {
  miriam-gene:9223 a ncit:C16612 .
  
  lld:C0025202 a ncit:C7057 .
  
  dgn-gda:DGNae3fd0b11cf4a174169c946d572c93f1 sio:SIO_000628 miriam-gene:9223, lld:C0025202;
    a sio:SIO_001121 .
}

dgn-np:NP216551.RAmbKFt2Dy3dYU2ByZUd4GM9v-tAUOhAfhTgvbzXTHVJs130_provenance {
  dgn-np:NP216551.RAmbKFt2Dy3dYU2ByZUd4GM9v-tAUOhAfhTgvbzXTHVJs130_assertion dcterms:description
      "[Herein are illustrated some pitfalls in the diagnosis of melanoma, as well as variants of Spitz's nevus that correlate with specific genomic aberrations such as gains of chromosome 11p and loss of the BAP-1 gene on chromosome 3p.]. 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:22648325;
    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:NP216551.RAmbKFt2Dy3dYU2ByZUd4GM9v-tAUOhAfhTgvbzXTHVJs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:00+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" .
}