@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP818022.RAq_R5Zm0ECos0qH_5a1drafy6xKRlaG4wWWi0vGQRMh8> .
@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:NP818022.RAq_R5Zm0ECos0qH_5a1drafy6xKRlaG4wWWi0vGQRMh8130_head {
  this: np:hasAssertion dgn-np:NP818022.RAq_R5Zm0ECos0qH_5a1drafy6xKRlaG4wWWi0vGQRMh8130_assertion;
    np:hasProvenance dgn-np:NP818022.RAq_R5Zm0ECos0qH_5a1drafy6xKRlaG4wWWi0vGQRMh8130_provenance;
    np:hasPublicationInfo dgn-np:NP818022.RAq_R5Zm0ECos0qH_5a1drafy6xKRlaG4wWWi0vGQRMh8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP818022.RAq_R5Zm0ECos0qH_5a1drafy6xKRlaG4wWWi0vGQRMh8130_assertion a np:Assertion .
  
  dgn-np:NP818022.RAq_R5Zm0ECos0qH_5a1drafy6xKRlaG4wWWi0vGQRMh8130_provenance a np:Provenance .
  
  dgn-np:NP818022.RAq_R5Zm0ECos0qH_5a1drafy6xKRlaG4wWWi0vGQRMh8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP818022.RAq_R5Zm0ECos0qH_5a1drafy6xKRlaG4wWWi0vGQRMh8130_assertion {
  miriam-gene:4157 a ncit:C16612 .
  
  lld:C0025202 a ncit:C7057 .
  
  dgn-gda:DGN68c19337adf982fae0318935ba5a0114 sio:SIO_000628 miriam-gene:4157, lld:C0025202;
    a sio:SIO_001121 .
}

dgn-np:NP818022.RAq_R5Zm0ECos0qH_5a1drafy6xKRlaG4wWWi0vGQRMh8130_provenance {
  dgn-np:NP818022.RAq_R5Zm0ECos0qH_5a1drafy6xKRlaG4wWWi0vGQRMh8130_assertion dcterms:description
      "[This study proposes the relevance of loss of function MC1R variants in the risk of melanoma in multiple primary melanoma cases with family history from areas with low melanoma incidence rate.]. 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:20539244;
    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:NP818022.RAq_R5Zm0ECos0qH_5a1drafy6xKRlaG4wWWi0vGQRMh8130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:55+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:disgenetv3.0rdf;
    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" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}