@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP603119.RAzw0P_pNEdmib1xbxHeumd47sBEd23byhe7EKt3FGPqY> .
@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:NP603119.RAzw0P_pNEdmib1xbxHeumd47sBEd23byhe7EKt3FGPqY130_head {
  this: np:hasAssertion dgn-np:NP603119.RAzw0P_pNEdmib1xbxHeumd47sBEd23byhe7EKt3FGPqY130_assertion;
    np:hasProvenance dgn-np:NP603119.RAzw0P_pNEdmib1xbxHeumd47sBEd23byhe7EKt3FGPqY130_provenance;
    np:hasPublicationInfo dgn-np:NP603119.RAzw0P_pNEdmib1xbxHeumd47sBEd23byhe7EKt3FGPqY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP603119.RAzw0P_pNEdmib1xbxHeumd47sBEd23byhe7EKt3FGPqY130_assertion a np:Assertion .
  
  dgn-np:NP603119.RAzw0P_pNEdmib1xbxHeumd47sBEd23byhe7EKt3FGPqY130_provenance a np:Provenance .
  
  dgn-np:NP603119.RAzw0P_pNEdmib1xbxHeumd47sBEd23byhe7EKt3FGPqY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP603119.RAzw0P_pNEdmib1xbxHeumd47sBEd23byhe7EKt3FGPqY130_assertion {
  miriam-gene:5429 a ncit:C16612 .
  
  lld:C0596263 a ncit:C7057 .
  
  dgn-gda:DGNabbc0a1cf32f7014341447c671d61dda sio:SIO_000628 miriam-gene:5429, lld:C0596263;
    a sio:SIO_001121 .
}

dgn-np:NP603119.RAzw0P_pNEdmib1xbxHeumd47sBEd23byhe7EKt3FGPqY130_provenance {
  dgn-np:NP603119.RAzw0P_pNEdmib1xbxHeumd47sBEd23byhe7EKt3FGPqY130_assertion dcterms:description
      "[Lack of DNA polymerase eta and the attendant defect in bypass replication of pyrimidine dimers induced in DNA by ultraviolet light (UV) underlie the enhanced mutagenesis and carcinogenesis observed in xeroderma pigmentosum variant (XP-V).]. 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:12082017;
    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:NP603119.RAzw0P_pNEdmib1xbxHeumd47sBEd23byhe7EKt3FGPqY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:02+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" .
}