@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP653317.RAeyaHP2hX8zf-aFbYritaesDGNO1ym9VnOrMi5L3lHuA> .
@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:NP653317.RAeyaHP2hX8zf-aFbYritaesDGNO1ym9VnOrMi5L3lHuA130_head {
  this: np:hasAssertion dgn-np:NP653317.RAeyaHP2hX8zf-aFbYritaesDGNO1ym9VnOrMi5L3lHuA130_assertion;
    np:hasProvenance dgn-np:NP653317.RAeyaHP2hX8zf-aFbYritaesDGNO1ym9VnOrMi5L3lHuA130_provenance;
    np:hasPublicationInfo dgn-np:NP653317.RAeyaHP2hX8zf-aFbYritaesDGNO1ym9VnOrMi5L3lHuA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP653317.RAeyaHP2hX8zf-aFbYritaesDGNO1ym9VnOrMi5L3lHuA130_assertion a np:Assertion .
  
  dgn-np:NP653317.RAeyaHP2hX8zf-aFbYritaesDGNO1ym9VnOrMi5L3lHuA130_provenance a np:Provenance .
  
  dgn-np:NP653317.RAeyaHP2hX8zf-aFbYritaesDGNO1ym9VnOrMi5L3lHuA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP653317.RAeyaHP2hX8zf-aFbYritaesDGNO1ym9VnOrMi5L3lHuA130_assertion {
  miriam-gene:4157 a ncit:C16612 .
  
  lld:C0041834 a ncit:C7057 .
  
  dgn-gda:DGN776b38c1dfad57028039fd3c4aa8e19d sio:SIO_000628 miriam-gene:4157, lld:C0041834;
    a sio:SIO_001121 .
}

dgn-np:NP653317.RAeyaHP2hX8zf-aFbYritaesDGNO1ym9VnOrMi5L3lHuA130_provenance {
  dgn-np:NP653317.RAeyaHP2hX8zf-aFbYritaesDGNO1ym9VnOrMi5L3lHuA130_assertion dcterms:description
      "[Persons carrying MC1R homozygote variant alleles at R151C, R160W, D294H and D84E were more likely to have fair skin, red hair and to spend less time outdoors than those who did not.]. 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:20129839;
    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:NP653317.RAeyaHP2hX8zf-aFbYritaesDGNO1ym9VnOrMi5L3lHuA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:33+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" .
}