@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP570490.RAuY022YxG8DL2ps6Hnu1GbvUklyXPgCS4mB_MODOqv6k> .
@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:NP570490.RAuY022YxG8DL2ps6Hnu1GbvUklyXPgCS4mB_MODOqv6k130_head {
  this: np:hasAssertion dgn-np:NP570490.RAuY022YxG8DL2ps6Hnu1GbvUklyXPgCS4mB_MODOqv6k130_assertion;
    np:hasProvenance dgn-np:NP570490.RAuY022YxG8DL2ps6Hnu1GbvUklyXPgCS4mB_MODOqv6k130_provenance;
    np:hasPublicationInfo dgn-np:NP570490.RAuY022YxG8DL2ps6Hnu1GbvUklyXPgCS4mB_MODOqv6k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP570490.RAuY022YxG8DL2ps6Hnu1GbvUklyXPgCS4mB_MODOqv6k130_assertion a np:Assertion .
  
  dgn-np:NP570490.RAuY022YxG8DL2ps6Hnu1GbvUklyXPgCS4mB_MODOqv6k130_provenance a np:Provenance .
  
  dgn-np:NP570490.RAuY022YxG8DL2ps6Hnu1GbvUklyXPgCS4mB_MODOqv6k130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP570490.RAuY022YxG8DL2ps6Hnu1GbvUklyXPgCS4mB_MODOqv6k130_assertion {
  miriam-gene:4157 a ncit:C16612 .
  
  lld:C0033860 a ncit:C7057 .
  
  dgn-gda:DGN308f8feda2f2c6a29a58cbafce086782 sio:SIO_000628 miriam-gene:4157, lld:C0033860;
    a sio:SIO_001121 .
}

dgn-np:NP570490.RAuY022YxG8DL2ps6Hnu1GbvUklyXPgCS4mB_MODOqv6k130_provenance {
  dgn-np:NP570490.RAuY022YxG8DL2ps6Hnu1GbvUklyXPgCS4mB_MODOqv6k130_assertion dcterms:description
      "[We used TaqMan quantitative gene copy and allelic discrimination assays to determine GST and MC1R genotypes, and looked for possible associations between genotype and threshold erythemal sensitivity (MED) and treatment outcomes in patients with psoriasis (n=256).]. 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:20802377;
    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:NP570490.RAuY022YxG8DL2ps6Hnu1GbvUklyXPgCS4mB_MODOqv6k130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:44+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" .
}