@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP71745.RAqY8oqJRnFIiJTNyOFjgt0a6m_iPN12acEt8Pz3FzRE4> .
@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:NP71745.RAqY8oqJRnFIiJTNyOFjgt0a6m_iPN12acEt8Pz3FzRE4130_head {
   this: np:hasAssertion dgn-np:NP71745.RAqY8oqJRnFIiJTNyOFjgt0a6m_iPN12acEt8Pz3FzRE4130_assertion ;
    np:hasProvenance dgn-np:NP71745.RAqY8oqJRnFIiJTNyOFjgt0a6m_iPN12acEt8Pz3FzRE4130_provenance ;
    np:hasPublicationInfo dgn-np:NP71745.RAqY8oqJRnFIiJTNyOFjgt0a6m_iPN12acEt8Pz3FzRE4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP71745.RAqY8oqJRnFIiJTNyOFjgt0a6m_iPN12acEt8Pz3FzRE4130_assertion a np:Assertion .
  dgn-np:NP71745.RAqY8oqJRnFIiJTNyOFjgt0a6m_iPN12acEt8Pz3FzRE4130_provenance a np:Provenance .
  dgn-np:NP71745.RAqY8oqJRnFIiJTNyOFjgt0a6m_iPN12acEt8Pz3FzRE4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP71745.RAqY8oqJRnFIiJTNyOFjgt0a6m_iPN12acEt8Pz3FzRE4130_assertion {
   miriam-gene:3662 a ncit:C16612 .
  lld:C0025202 a ncit:C7057 .
  dgn-gda:DGN0bf649a19e7cb6a1e165f24742879905 sio:SIO_000628 miriam-gene:3662 , lld:C0025202 ;
    a sio:SIO_001122 .
}
dgn-np:NP71745.RAqY8oqJRnFIiJTNyOFjgt0a6m_iPN12acEt8Pz3FzRE4130_provenance {
   dgn-np:NP71745.RAqY8oqJRnFIiJTNyOFjgt0a6m_iPN12acEt8Pz3FzRE4130_assertion dcterms: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:NP71745.RAqY8oqJRnFIiJTNyOFjgt0a6m_iPN12acEt8Pz3FzRE4130_publicationInfo {
   this: dcterms:created "2014-10-02T12:32:35+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" .
}