@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP55560.RARv6BS-sOu0FpgrglmnuTc_4fGKvCYzqT74yNd5bhvVM> .
@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:NP55560.RARv6BS-sOu0FpgrglmnuTc_4fGKvCYzqT74yNd5bhvVM130_head {
  this: np:hasAssertion dgn-np:NP55560.RARv6BS-sOu0FpgrglmnuTc_4fGKvCYzqT74yNd5bhvVM130_assertion;
    np:hasProvenance dgn-np:NP55560.RARv6BS-sOu0FpgrglmnuTc_4fGKvCYzqT74yNd5bhvVM130_provenance;
    np:hasPublicationInfo dgn-np:NP55560.RARv6BS-sOu0FpgrglmnuTc_4fGKvCYzqT74yNd5bhvVM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP55560.RARv6BS-sOu0FpgrglmnuTc_4fGKvCYzqT74yNd5bhvVM130_assertion a np:Assertion .
  
  dgn-np:NP55560.RARv6BS-sOu0FpgrglmnuTc_4fGKvCYzqT74yNd5bhvVM130_provenance a np:Provenance .
  
  dgn-np:NP55560.RARv6BS-sOu0FpgrglmnuTc_4fGKvCYzqT74yNd5bhvVM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP55560.RARv6BS-sOu0FpgrglmnuTc_4fGKvCYzqT74yNd5bhvVM130_assertion {
  miriam-gene:3803 a ncit:C16612 .
  
  lld:C0025202 a ncit:C7057 .
  
  dgn-gda:DGN0828a7f09977fbf22f557a4395ef952f sio:SIO_000628 miriam-gene:3803, lld:C0025202;
    a sio:SIO_001122 .
}

dgn-np:NP55560.RARv6BS-sOu0FpgrglmnuTc_4fGKvCYzqT74yNd5bhvVM130_provenance {
  dgn-np:NP55560.RARv6BS-sOu0FpgrglmnuTc_4fGKvCYzqT74yNd5bhvVM130_assertion dcterms:description
      "[The data obtained in this study imply that there may not be a direct association between KIR gene content in the genome and the presence of malignant melanoma, or melanoma progression. However, some HLA haplotypes could be predisposing to MM in the Bulgarian population. Furthermore, distinct KIR/HLA ligand combinations may be relevant to the development of malignancy whereby inhibition overrides activation of NK cells and T cells expressing NK-associated receptors, which in turn might facilitate tumor escape and progression.]. 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:15248031;
    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:NP55560.RARv6BS-sOu0FpgrglmnuTc_4fGKvCYzqT74yNd5bhvVM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:26+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" .
}