@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP661771.RAlXVzwzUdH7y06_4UJe1Cmg2bD8aATrfGrFHqWYQAEbM> .
@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:NP661771.RAlXVzwzUdH7y06_4UJe1Cmg2bD8aATrfGrFHqWYQAEbM130_head {
  this: np:hasAssertion dgn-np:NP661771.RAlXVzwzUdH7y06_4UJe1Cmg2bD8aATrfGrFHqWYQAEbM130_assertion;
    np:hasProvenance dgn-np:NP661771.RAlXVzwzUdH7y06_4UJe1Cmg2bD8aATrfGrFHqWYQAEbM130_provenance;
    np:hasPublicationInfo dgn-np:NP661771.RAlXVzwzUdH7y06_4UJe1Cmg2bD8aATrfGrFHqWYQAEbM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP661771.RAlXVzwzUdH7y06_4UJe1Cmg2bD8aATrfGrFHqWYQAEbM130_assertion a np:Assertion .
  
  dgn-np:NP661771.RAlXVzwzUdH7y06_4UJe1Cmg2bD8aATrfGrFHqWYQAEbM130_provenance a np:Provenance .
  
  dgn-np:NP661771.RAlXVzwzUdH7y06_4UJe1Cmg2bD8aATrfGrFHqWYQAEbM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP661771.RAlXVzwzUdH7y06_4UJe1Cmg2bD8aATrfGrFHqWYQAEbM130_assertion {
  miriam-gene:9455 a ncit:C16612 .
  
  lld:C0043346 a ncit:C7057 .
  
  dgn-gda:DGNe7e478a3e379d185c97af1c445ac6bb7 sio:SIO_000628 miriam-gene:9455, lld:C0043346;
    a sio:SIO_001121 .
}

dgn-np:NP661771.RAlXVzwzUdH7y06_4UJe1Cmg2bD8aATrfGrFHqWYQAEbM130_provenance {
  dgn-np:NP661771.RAlXVzwzUdH7y06_4UJe1Cmg2bD8aATrfGrFHqWYQAEbM130_assertion dcterms:description
      "[The action spectrum for erythema parallels the action spectrum for CPD formation in skin, and in the absence of repair, as in the genetic disease xeroderma pigmentosum (XP), skin cancer rates are dramatically increased.]. 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:15603216;
    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:NP661771.RAlXVzwzUdH7y06_4UJe1Cmg2bD8aATrfGrFHqWYQAEbM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:40+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" .
}