@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP281924.RAOZXaR0I9WUetjmgJeNau7PgiLVVqSRnw-4W9g6MaQ9s> .
@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:NP281924.RAOZXaR0I9WUetjmgJeNau7PgiLVVqSRnw-4W9g6MaQ9s130_head {
  this: np:hasAssertion dgn-np:NP281924.RAOZXaR0I9WUetjmgJeNau7PgiLVVqSRnw-4W9g6MaQ9s130_assertion ;
    np:hasProvenance dgn-np:NP281924.RAOZXaR0I9WUetjmgJeNau7PgiLVVqSRnw-4W9g6MaQ9s130_provenance ;
    np:hasPublicationInfo dgn-np:NP281924.RAOZXaR0I9WUetjmgJeNau7PgiLVVqSRnw-4W9g6MaQ9s130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP281924.RAOZXaR0I9WUetjmgJeNau7PgiLVVqSRnw-4W9g6MaQ9s130_assertion a np:Assertion .
  dgn-np:NP281924.RAOZXaR0I9WUetjmgJeNau7PgiLVVqSRnw-4W9g6MaQ9s130_provenance a np:Provenance .
  dgn-np:NP281924.RAOZXaR0I9WUetjmgJeNau7PgiLVVqSRnw-4W9g6MaQ9s130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP281924.RAOZXaR0I9WUetjmgJeNau7PgiLVVqSRnw-4W9g6MaQ9s130_assertion {
  miriam-gene:1029 a ncit:C16612 .
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    a sio:SIO_001121 .
}
dgn-np:NP281924.RAOZXaR0I9WUetjmgJeNau7PgiLVVqSRnw-4W9g6MaQ9s130_provenance {
  dgn-np:NP281924.RAOZXaR0I9WUetjmgJeNau7PgiLVVqSRnw-4W9g6MaQ9s130_assertion dcterms:description "[These recent advances open up the possibility of genetic testing for melanoma susceptibility in the setting of familial melanoma and suggest novel therapeutic strategies for melanoma based on gene therapy or small molecule mimicry targeted to the correction of defects in the p16 regulatory pathway.]. 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:10775844 ;
    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:NP281924.RAOZXaR0I9WUetjmgJeNau7PgiLVVqSRnw-4W9g6MaQ9s130_publicationInfo {
  this: dcterms:created "2016-05-13T12:43:53+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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    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" .
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}