@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP299736.RAR2gNv-cBZzLdXrEVFoVk6NfXEox4PqoC8EspjzG9nAY> .
@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:NP299736.RAR2gNv-cBZzLdXrEVFoVk6NfXEox4PqoC8EspjzG9nAY130_head {
  this: np:hasAssertion dgn-np:NP299736.RAR2gNv-cBZzLdXrEVFoVk6NfXEox4PqoC8EspjzG9nAY130_assertion;
    np:hasProvenance dgn-np:NP299736.RAR2gNv-cBZzLdXrEVFoVk6NfXEox4PqoC8EspjzG9nAY130_provenance;
    np:hasPublicationInfo dgn-np:NP299736.RAR2gNv-cBZzLdXrEVFoVk6NfXEox4PqoC8EspjzG9nAY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP299736.RAR2gNv-cBZzLdXrEVFoVk6NfXEox4PqoC8EspjzG9nAY130_assertion a np:Assertion .
  
  dgn-np:NP299736.RAR2gNv-cBZzLdXrEVFoVk6NfXEox4PqoC8EspjzG9nAY130_provenance a np:Provenance .
  
  dgn-np:NP299736.RAR2gNv-cBZzLdXrEVFoVk6NfXEox4PqoC8EspjzG9nAY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP299736.RAR2gNv-cBZzLdXrEVFoVk6NfXEox4PqoC8EspjzG9nAY130_assertion {
  miriam-gene:100913187 a ncit:C16612 .
  
  lld:C0007114 a ncit:C7057 .
  
  dgn-gda:DGN2ee30e4186e2627443f81e5e87a28d8e sio:SIO_000628 miriam-gene:100913187,
      lld:C0007114;
    a sio:SIO_001121 .
}

dgn-np:NP299736.RAR2gNv-cBZzLdXrEVFoVk6NfXEox4PqoC8EspjzG9nAY130_provenance {
  dgn-np:NP299736.RAR2gNv-cBZzLdXrEVFoVk6NfXEox4PqoC8EspjzG9nAY130_assertion dcterms:description
      "[The biochemical data taken in conjunction with the biological up-regulation of Apo3A in skin lesions suggests that enzyme-catalyzed deaminations at adjacent C sites followed by normal replication generating CC → TT mutations provides an alternative molecular basis for the initiation events in skin cancer in contrast to well established pathways in which CC dimers formed in response to UV radiation either undergo nonenzymatic spontaneous deaminations or aberrant replication.]. 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:23979356;
    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:NP299736.RAR2gNv-cBZzLdXrEVFoVk6NfXEox4PqoC8EspjzG9nAY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:50+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" .
}