@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP322237.RApVn7BvtGVmkUmMN5uL-GF6EXEGmjn6slCgTVZbA8x_k> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP322237.RApVn7BvtGVmkUmMN5uL-GF6EXEGmjn6slCgTVZbA8x_k130_head {
  this: np:hasAssertion dgn-np:NP322237.RApVn7BvtGVmkUmMN5uL-GF6EXEGmjn6slCgTVZbA8x_k130_assertion;
    np:hasProvenance dgn-np:NP322237.RApVn7BvtGVmkUmMN5uL-GF6EXEGmjn6slCgTVZbA8x_k130_provenance;
    np:hasPublicationInfo dgn-np:NP322237.RApVn7BvtGVmkUmMN5uL-GF6EXEGmjn6slCgTVZbA8x_k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP322237.RApVn7BvtGVmkUmMN5uL-GF6EXEGmjn6slCgTVZbA8x_k130_assertion a np:Assertion .
  
  dgn-np:NP322237.RApVn7BvtGVmkUmMN5uL-GF6EXEGmjn6slCgTVZbA8x_k130_provenance a np:Provenance .
  
  dgn-np:NP322237.RApVn7BvtGVmkUmMN5uL-GF6EXEGmjn6slCgTVZbA8x_k130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP322237.RApVn7BvtGVmkUmMN5uL-GF6EXEGmjn6slCgTVZbA8x_k130_assertion {
  miriam-gene:1312 a ncit:C16612 .
  
  lld:C1847835 a ncit:C7057 .
  
  dgn-gda:DGN83eb6e949dc8e3345a69d5cf465b9136 sio:SIO_000628 miriam-gene:1312, lld:C1847835;
    a sio:SIO_001121 .
}

dgn-np:NP322237.RApVn7BvtGVmkUmMN5uL-GF6EXEGmjn6slCgTVZbA8x_k130_provenance {
  dgn-np:NP322237.RApVn7BvtGVmkUmMN5uL-GF6EXEGmjn6slCgTVZbA8x_k130_assertion dcterms:description
      "[In conclusion, the enhanced oxidative stress with the lack of association between CAT and COMT polymorphisms and susceptibility to vitiligo in our patients suggest that mutations in other genes related to the oxidative pathway might contribute to the etiology of generalized vitiligo in Egyptian population.]. 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:24915010;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP322237.RApVn7BvtGVmkUmMN5uL-GF6EXEGmjn6slCgTVZbA8x_k130_publicationInfo {
  this: dcterms:created "2015-08-25T14:40:45+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}