@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP749995.RA7glDdYgOvjPfYXMIFl7QQwcsyBm-fSUvnYJ9ZwjTPQM> .
@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:NP749995.RA7glDdYgOvjPfYXMIFl7QQwcsyBm-fSUvnYJ9ZwjTPQM130_assertion;
    np:hasProvenance dgn-np:NP749995.RA7glDdYgOvjPfYXMIFl7QQwcsyBm-fSUvnYJ9ZwjTPQM130_provenance;
    np:hasPublicationInfo dgn-np:NP749995.RA7glDdYgOvjPfYXMIFl7QQwcsyBm-fSUvnYJ9ZwjTPQM130_publicationInfo;
    a np:Nanopublication .
  
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dgn-np:NP749995.RA7glDdYgOvjPfYXMIFl7QQwcsyBm-fSUvnYJ9ZwjTPQM130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C0205748 a ncit:C7057 .
  
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dgn-np:NP749995.RA7glDdYgOvjPfYXMIFl7QQwcsyBm-fSUvnYJ9ZwjTPQM130_provenance {
  dgn-np:NP749995.RA7glDdYgOvjPfYXMIFl7QQwcsyBm-fSUvnYJ9ZwjTPQM130_assertion dcterms:description
      "[This article reviews p53 alterations (at the gene and protein levels) in melanocytic skin lesions and discusses the following points: (i) p53 alterations commence as early as at the stage of benign and dysplastic nevi; (ii) these alterations are frequent in melanomas, and gradually increase with their progression; (iii) there is no concordance between the frequent p53 protein expression and the rarity of both TP53 gene mutations in melanomas, and (iv) the entire p53 pathway is a more critical determinant of the fate of the melanocytic skin lesions than the status of the p53 protein or the gene itself.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
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    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
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dgn-np:NP749995.RA7glDdYgOvjPfYXMIFl7QQwcsyBm-fSUvnYJ9ZwjTPQM130_publicationInfo {
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    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
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    prv:usedData dgn-void:disgenetrdf;
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