@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP484250.RApBSeq_NXPlr9ZmMycQQwbm1Zc6ZeXVNAK_sOJ-pbdCg> .
@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:NP484250.RApBSeq_NXPlr9ZmMycQQwbm1Zc6ZeXVNAK_sOJ-pbdCg130_head {
  this: np:hasAssertion dgn-np:NP484250.RApBSeq_NXPlr9ZmMycQQwbm1Zc6ZeXVNAK_sOJ-pbdCg130_assertion;
    np:hasProvenance dgn-np:NP484250.RApBSeq_NXPlr9ZmMycQQwbm1Zc6ZeXVNAK_sOJ-pbdCg130_provenance;
    np:hasPublicationInfo dgn-np:NP484250.RApBSeq_NXPlr9ZmMycQQwbm1Zc6ZeXVNAK_sOJ-pbdCg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP484250.RApBSeq_NXPlr9ZmMycQQwbm1Zc6ZeXVNAK_sOJ-pbdCg130_assertion a np:Assertion .
  
  dgn-np:NP484250.RApBSeq_NXPlr9ZmMycQQwbm1Zc6ZeXVNAK_sOJ-pbdCg130_provenance a np:Provenance .
  
  dgn-np:NP484250.RApBSeq_NXPlr9ZmMycQQwbm1Zc6ZeXVNAK_sOJ-pbdCg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP484250.RApBSeq_NXPlr9ZmMycQQwbm1Zc6ZeXVNAK_sOJ-pbdCg130_assertion {
  miriam-gene:6006 a ncit:C16612 .
  
  lld:C0025202 a ncit:C7057 .
  
  dgn-gda:DGN1288cfcbd1ef2e3a4f4ffc1046295ecf sio:SIO_000628 miriam-gene:6006, lld:C0025202;
    a sio:SIO_001121 .
}

dgn-np:NP484250.RApBSeq_NXPlr9ZmMycQQwbm1Zc6ZeXVNAK_sOJ-pbdCg130_provenance {
  dgn-np:NP484250.RApBSeq_NXPlr9ZmMycQQwbm1Zc6ZeXVNAK_sOJ-pbdCg130_assertion dcterms:description
      "[In conclusion, our results show without ambiguity that in South European populations, MC1R RHC and SCL45A2 p.Phe374Leu variants are strong melanoma risk predictors, notably in those individuals who would not be identified as high risk based on their phenotypes or exposures alone.]. 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:22464347;
    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:NP484250.RApBSeq_NXPlr9ZmMycQQwbm1Zc6ZeXVNAK_sOJ-pbdCg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:49+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" .
}