@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP534771.RALOxlQ-Fm1Dch0loAcAwUEjsM5696r3PqjNFxXp2LHPw> .
@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:NP534771.RALOxlQ-Fm1Dch0loAcAwUEjsM5696r3PqjNFxXp2LHPw130_head {
  this: np:hasAssertion dgn-np:NP534771.RALOxlQ-Fm1Dch0loAcAwUEjsM5696r3PqjNFxXp2LHPw130_assertion;
    np:hasProvenance dgn-np:NP534771.RALOxlQ-Fm1Dch0loAcAwUEjsM5696r3PqjNFxXp2LHPw130_provenance;
    np:hasPublicationInfo dgn-np:NP534771.RALOxlQ-Fm1Dch0loAcAwUEjsM5696r3PqjNFxXp2LHPw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP534771.RALOxlQ-Fm1Dch0loAcAwUEjsM5696r3PqjNFxXp2LHPw130_assertion a np:Assertion .
  
  dgn-np:NP534771.RALOxlQ-Fm1Dch0loAcAwUEjsM5696r3PqjNFxXp2LHPw130_provenance a np:Provenance .
  
  dgn-np:NP534771.RALOxlQ-Fm1Dch0loAcAwUEjsM5696r3PqjNFxXp2LHPw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP534771.RALOxlQ-Fm1Dch0loAcAwUEjsM5696r3PqjNFxXp2LHPw130_assertion {
  miriam-gene:6298 a ncit:C16612 .
  
  lld:C0025202 a ncit:C7057 .
  
  dgn-gda:DGN652bd6b32fd5c6546006ea3a3fb11c3d sio:SIO_000628 miriam-gene:6298, lld:C0025202;
    a sio:SIO_001121 .
}

dgn-np:NP534771.RALOxlQ-Fm1Dch0loAcAwUEjsM5696r3PqjNFxXp2LHPw130_provenance {
  dgn-np:NP534771.RALOxlQ-Fm1Dch0loAcAwUEjsM5696r3PqjNFxXp2LHPw130_assertion dcterms:description
      "[These data indicate correlation between gradual loss of expression of the MTS1 locus and progression of melanoma, further supporting an emerging role for the gene in the malignant transformation of melanocytes.]. 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:9620301;
    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:NP534771.RALOxlQ-Fm1Dch0loAcAwUEjsM5696r3PqjNFxXp2LHPw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:23+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" .
}