@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP257857.RAOOywwudXOICjZm41F7i-j3hIKDy8RnqIBVhY0H2B4RE> .
@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#> .
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   this: np:hasAssertion dgn-np:NP257857.RAOOywwudXOICjZm41F7i-j3hIKDy8RnqIBVhY0H2B4RE130_assertion ;
    np:hasProvenance dgn-np:NP257857.RAOOywwudXOICjZm41F7i-j3hIKDy8RnqIBVhY0H2B4RE130_provenance ;
    np:hasPublicationInfo dgn-np:NP257857.RAOOywwudXOICjZm41F7i-j3hIKDy8RnqIBVhY0H2B4RE130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP257857.RAOOywwudXOICjZm41F7i-j3hIKDy8RnqIBVhY0H2B4RE130_provenance a np:Provenance .
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}
dgn-np:NP257857.RAOOywwudXOICjZm41F7i-j3hIKDy8RnqIBVhY0H2B4RE130_assertion {
   miriam-gene:56288 a ncit:C16612 .
  lld:C0151779 a ncit:C7057 .
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    a sio:SIO_001121 .
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dgn-np:NP257857.RAOOywwudXOICjZm41F7i-j3hIKDy8RnqIBVhY0H2B4RE130_provenance {
   dgn-np:NP257857.RAOOywwudXOICjZm41F7i-j3hIKDy8RnqIBVhY0H2B4RE130_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 ;
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  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:NP257857.RAOOywwudXOICjZm41F7i-j3hIKDy8RnqIBVhY0H2B4RE130_publicationInfo {
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    dcterms:rightsHolder dgn-void:IBIGroup ;
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    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> ;
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