@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP47006.RAx99QyvtLo9Ig-Ky1_a4N6FWfg0vJy2rD_5u6A7J9KMM> .
@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:NP47006.RAx99QyvtLo9Ig-Ky1_a4N6FWfg0vJy2rD_5u6A7J9KMM130_head {
  this: np:hasAssertion dgn-np:NP47006.RAx99QyvtLo9Ig-Ky1_a4N6FWfg0vJy2rD_5u6A7J9KMM130_assertion;
    np:hasProvenance dgn-np:NP47006.RAx99QyvtLo9Ig-Ky1_a4N6FWfg0vJy2rD_5u6A7J9KMM130_provenance;
    np:hasPublicationInfo dgn-np:NP47006.RAx99QyvtLo9Ig-Ky1_a4N6FWfg0vJy2rD_5u6A7J9KMM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP47006.RAx99QyvtLo9Ig-Ky1_a4N6FWfg0vJy2rD_5u6A7J9KMM130_assertion a np:Assertion .
  
  dgn-np:NP47006.RAx99QyvtLo9Ig-Ky1_a4N6FWfg0vJy2rD_5u6A7J9KMM130_provenance a np:Provenance .
  
  dgn-np:NP47006.RAx99QyvtLo9Ig-Ky1_a4N6FWfg0vJy2rD_5u6A7J9KMM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP47006.RAx99QyvtLo9Ig-Ky1_a4N6FWfg0vJy2rD_5u6A7J9KMM130_assertion {
  miriam-gene:1030 a ncit:C16612 .
  
  lld:C0025202 a ncit:C7057 .
  
  dgn-gda:DGNce06b1a14aebdc3350d8fd58641032f5 sio:SIO_000628 miriam-gene:1030, lld:C0025202;
    a sio:SIO_001122 .
}

dgn-np:NP47006.RAx99QyvtLo9Ig-Ky1_a4N6FWfg0vJy2rD_5u6A7J9KMM130_provenance {
  dgn-np:NP47006.RAx99QyvtLo9Ig-Ky1_a4N6FWfg0vJy2rD_5u6A7J9KMM130_assertion dcterms:description
      "[The aims of our study were to analyse alterations in p53, p21, p16 and p15 genes in melanoma tumors and melanoma cell lines by single strand conformational polymorphism (SSCP), and to detect homozygous deletions.]. 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:15960923;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP47006.RAx99QyvtLo9Ig-Ky1_a4N6FWfg0vJy2rD_5u6A7J9KMM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:21+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" .
}