@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP78733.RAxr4CGBYIe7H6r0d5wvPf4DPCt1OQbNNfQRe0JvPUYA0> .
@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 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:NP78733.RAxr4CGBYIe7H6r0d5wvPf4DPCt1OQbNNfQRe0JvPUYA0130_head {
  this: np:hasAssertion dgn-np:NP78733.RAxr4CGBYIe7H6r0d5wvPf4DPCt1OQbNNfQRe0JvPUYA0130_assertion;
    np:hasProvenance dgn-np:NP78733.RAxr4CGBYIe7H6r0d5wvPf4DPCt1OQbNNfQRe0JvPUYA0130_provenance;
    np:hasPublicationInfo dgn-np:NP78733.RAxr4CGBYIe7H6r0d5wvPf4DPCt1OQbNNfQRe0JvPUYA0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP78733.RAxr4CGBYIe7H6r0d5wvPf4DPCt1OQbNNfQRe0JvPUYA0130_assertion a np:Assertion .
  
  dgn-np:NP78733.RAxr4CGBYIe7H6r0d5wvPf4DPCt1OQbNNfQRe0JvPUYA0130_provenance a np:Provenance .
  
  dgn-np:NP78733.RAxr4CGBYIe7H6r0d5wvPf4DPCt1OQbNNfQRe0JvPUYA0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP78733.RAxr4CGBYIe7H6r0d5wvPf4DPCt1OQbNNfQRe0JvPUYA0130_assertion {
  miriam-gene:51151 a ncit:C16612 .
  
  lld:C0025202 a ncit:C7057 .
  
  dgn-gda:DGNb22bbab6fa11044443a07be7d7e06d02 sio:SIO_000628 miriam-gene:51151, lld:C0025202;
    a sio:SIO_001122 .
}

dgn-np:NP78733.RAxr4CGBYIe7H6r0d5wvPf4DPCt1OQbNNfQRe0JvPUYA0130_provenance {
  dgn-np:NP78733.RAxr4CGBYIe7H6r0d5wvPf4DPCt1OQbNNfQRe0JvPUYA0130_assertion dct:description
      "[In this paper, we test a selected set of polymorphisms in pigmentation loci (ASIP (Agouti signalling protein, nonagouti homolog (mouse) gene), TYR (tyrosinase), TYRP1 (tyrosinase-related protein 1), MC1R, OCA2, IRF4 (interferon regulatory factor 4), SLC24A4 (solute carrier family 24, member 4), and SLC45A2 (solute carrier family 45, member 2)) for association with CMM risk in a large Australian population-based case-control study.]. 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:19710684;
    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:NP78733.RAxr4CGBYIe7H6r0d5wvPf4DPCt1OQbNNfQRe0JvPUYA0130_publicationInfo {
  this: dct:created "2014-10-02T12:32:38+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}