@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP709645.RASxYZ1jz2XFJ25LivFcjyW70Gz3Q4sSa1CVbECVFXduo> .
@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:NP709645.RASxYZ1jz2XFJ25LivFcjyW70Gz3Q4sSa1CVbECVFXduo130_head {
  this: np:hasAssertion dgn-np:NP709645.RASxYZ1jz2XFJ25LivFcjyW70Gz3Q4sSa1CVbECVFXduo130_assertion;
    np:hasProvenance dgn-np:NP709645.RASxYZ1jz2XFJ25LivFcjyW70Gz3Q4sSa1CVbECVFXduo130_provenance;
    np:hasPublicationInfo dgn-np:NP709645.RASxYZ1jz2XFJ25LivFcjyW70Gz3Q4sSa1CVbECVFXduo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP709645.RASxYZ1jz2XFJ25LivFcjyW70Gz3Q4sSa1CVbECVFXduo130_assertion a np:Assertion .
  
  dgn-np:NP709645.RASxYZ1jz2XFJ25LivFcjyW70Gz3Q4sSa1CVbECVFXduo130_provenance a np:Provenance .
  
  dgn-np:NP709645.RASxYZ1jz2XFJ25LivFcjyW70Gz3Q4sSa1CVbECVFXduo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP709645.RASxYZ1jz2XFJ25LivFcjyW70Gz3Q4sSa1CVbECVFXduo130_assertion {
  miriam-gene:7376 a ncit:C16612 .
  
  lld:C0011156 a ncit:C7057 .
  
  dgn-gda:DGN7736679bcfb9273019a0cc8aa9c6507a sio:SIO_000628 miriam-gene:7376, lld:C0011156;
    a sio:SIO_001121 .
}

dgn-np:NP709645.RASxYZ1jz2XFJ25LivFcjyW70Gz3Q4sSa1CVbECVFXduo130_provenance {
  dgn-np:NP709645.RASxYZ1jz2XFJ25LivFcjyW70Gz3Q4sSa1CVbECVFXduo130_assertion dcterms:description
      "[Subsequently Xpa and Xpc knockouts have proved to be good models for the human NER deficiency disease, xeroderma pigmentosum, leading to speculation that the recombination, rather than the NER deficit is the key to the Ercc1 knockout phenotype.]. 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:12466203;
    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:NP709645.RASxYZ1jz2XFJ25LivFcjyW70Gz3Q4sSa1CVbECVFXduo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:11+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" .
}