@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP270748.RALEU-jRYfDa2w8FWoZhz9fSudEjLMMfhL6AFPwV5DOHU> .
@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:NP270748.RALEU-jRYfDa2w8FWoZhz9fSudEjLMMfhL6AFPwV5DOHU130_head {
  this: np:hasAssertion dgn-np:NP270748.RALEU-jRYfDa2w8FWoZhz9fSudEjLMMfhL6AFPwV5DOHU130_assertion;
    np:hasProvenance dgn-np:NP270748.RALEU-jRYfDa2w8FWoZhz9fSudEjLMMfhL6AFPwV5DOHU130_provenance;
    np:hasPublicationInfo dgn-np:NP270748.RALEU-jRYfDa2w8FWoZhz9fSudEjLMMfhL6AFPwV5DOHU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP270748.RALEU-jRYfDa2w8FWoZhz9fSudEjLMMfhL6AFPwV5DOHU130_assertion a np:Assertion .
  
  dgn-np:NP270748.RALEU-jRYfDa2w8FWoZhz9fSudEjLMMfhL6AFPwV5DOHU130_provenance a np:Provenance .
  
  dgn-np:NP270748.RALEU-jRYfDa2w8FWoZhz9fSudEjLMMfhL6AFPwV5DOHU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP270748.RALEU-jRYfDa2w8FWoZhz9fSudEjLMMfhL6AFPwV5DOHU130_assertion {
  miriam-gene:4157 a ncit:C16612 .
  
  lld:C0007097 a ncit:C7057 .
  
  dgn-gda:DGN1e5f76db4461d2e9f7150c4946c17431 sio:SIO_000628 miriam-gene:4157, lld:C0007097;
    a sio:SIO_001121 .
}

dgn-np:NP270748.RALEU-jRYfDa2w8FWoZhz9fSudEjLMMfhL6AFPwV5DOHU130_provenance {
  dgn-np:NP270748.RALEU-jRYfDa2w8FWoZhz9fSudEjLMMfhL6AFPwV5DOHU130_assertion dcterms:description
      "[After adjusting for the effects of pigmentation on the association between MC1R variant alleles and basal cell carcinoma and squamous cell carcinoma risk, the association persisted, confirming that presence of at least one variant allele remains informative in terms of predicting risk for developing a solar-induced skin lesion beyond that information wained through observation of pigmentation phenotype.]. 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:11179997;
    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:NP270748.RALEU-jRYfDa2w8FWoZhz9fSudEjLMMfhL6AFPwV5DOHU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:31+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" .
}