@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP641533.RAc5EgAmzQsFfsbKdMJ41Okihrcf5sbIJ0ejtoZc9vmPM> .
@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:NP641533.RAc5EgAmzQsFfsbKdMJ41Okihrcf5sbIJ0ejtoZc9vmPM130_head {
  this: np:hasAssertion dgn-np:NP641533.RAc5EgAmzQsFfsbKdMJ41Okihrcf5sbIJ0ejtoZc9vmPM130_assertion;
    np:hasProvenance dgn-np:NP641533.RAc5EgAmzQsFfsbKdMJ41Okihrcf5sbIJ0ejtoZc9vmPM130_provenance;
    np:hasPublicationInfo dgn-np:NP641533.RAc5EgAmzQsFfsbKdMJ41Okihrcf5sbIJ0ejtoZc9vmPM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP641533.RAc5EgAmzQsFfsbKdMJ41Okihrcf5sbIJ0ejtoZc9vmPM130_assertion a np:Assertion .
  
  dgn-np:NP641533.RAc5EgAmzQsFfsbKdMJ41Okihrcf5sbIJ0ejtoZc9vmPM130_provenance a np:Provenance .
  
  dgn-np:NP641533.RAc5EgAmzQsFfsbKdMJ41Okihrcf5sbIJ0ejtoZc9vmPM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP641533.RAc5EgAmzQsFfsbKdMJ41Okihrcf5sbIJ0ejtoZc9vmPM130_assertion {
  miriam-gene:2952 a ncit:C16612 .
  
  lld:C0007114 a ncit:C7057 .
  
  dgn-gda:DGNc6cf305bdfd03cd0aeb1bf37978053c9 sio:SIO_000628 miriam-gene:2952, lld:C0007114;
    a sio:SIO_001121 .
}

dgn-np:NP641533.RAc5EgAmzQsFfsbKdMJ41Okihrcf5sbIJ0ejtoZc9vmPM130_provenance {
  dgn-np:NP641533.RAc5EgAmzQsFfsbKdMJ41Okihrcf5sbIJ0ejtoZc9vmPM130_assertion dcterms:description
      "[GSTM1 and GSTT1 are deleted in approximately 50 and 20% of the Caucasian population, respectively, and GST null genotype has been associated with increased sunburn sensitivity and reduced minimal erythemal dose (MED) after broadband UVR exposure in healthy volunteers and with susceptibility to skin cancer.]. 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:NP641533.RAc5EgAmzQsFfsbKdMJ41Okihrcf5sbIJ0ejtoZc9vmPM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:26+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" .
}