@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP584851.RAHYflVi9T7XITVV-pJMp0r4yBeBjjr5ZIzSkHyPTsLVY> .
@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#> .
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  this: np:hasAssertion dgn-np:NP584851.RAHYflVi9T7XITVV-pJMp0r4yBeBjjr5ZIzSkHyPTsLVY130_assertion ;
    np:hasProvenance dgn-np:NP584851.RAHYflVi9T7XITVV-pJMp0r4yBeBjjr5ZIzSkHyPTsLVY130_provenance ;
    np:hasPublicationInfo dgn-np:NP584851.RAHYflVi9T7XITVV-pJMp0r4yBeBjjr5ZIzSkHyPTsLVY130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP584851.RAHYflVi9T7XITVV-pJMp0r4yBeBjjr5ZIzSkHyPTsLVY130_provenance a np:Provenance .
  dgn-np:NP584851.RAHYflVi9T7XITVV-pJMp0r4yBeBjjr5ZIzSkHyPTsLVY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP584851.RAHYflVi9T7XITVV-pJMp0r4yBeBjjr5ZIzSkHyPTsLVY130_assertion {
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dgn-np:NP584851.RAHYflVi9T7XITVV-pJMp0r4yBeBjjr5ZIzSkHyPTsLVY130_provenance {
  dgn-np:NP584851.RAHYflVi9T7XITVV-pJMp0r4yBeBjjr5ZIzSkHyPTsLVY130_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 ;
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}
dgn-np:NP584851.RAHYflVi9T7XITVV-pJMp0r4yBeBjjr5ZIzSkHyPTsLVY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:52+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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