@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP309045.RAVwHhjTzVtE2JAfqZFIWZVZPy-rvA6Box9us5zLR4YGU> .
@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:NP309045.RAVwHhjTzVtE2JAfqZFIWZVZPy-rvA6Box9us5zLR4YGU130_head {
  this: np:hasAssertion dgn-np:NP309045.RAVwHhjTzVtE2JAfqZFIWZVZPy-rvA6Box9us5zLR4YGU130_assertion;
    np:hasProvenance dgn-np:NP309045.RAVwHhjTzVtE2JAfqZFIWZVZPy-rvA6Box9us5zLR4YGU130_provenance;
    np:hasPublicationInfo dgn-np:NP309045.RAVwHhjTzVtE2JAfqZFIWZVZPy-rvA6Box9us5zLR4YGU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP309045.RAVwHhjTzVtE2JAfqZFIWZVZPy-rvA6Box9us5zLR4YGU130_assertion a np:Assertion .
  
  dgn-np:NP309045.RAVwHhjTzVtE2JAfqZFIWZVZPy-rvA6Box9us5zLR4YGU130_provenance a np:Provenance .
  
  dgn-np:NP309045.RAVwHhjTzVtE2JAfqZFIWZVZPy-rvA6Box9us5zLR4YGU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP309045.RAVwHhjTzVtE2JAfqZFIWZVZPy-rvA6Box9us5zLR4YGU130_assertion {
  miriam-gene:2073 a ncit:C16612 .
  
  lld:C0009207 a ncit:C7057 .
  
  dgn-gda:DGN8c87e93910cd7d8aa493be42b0c9193e sio:SIO_000628 miriam-gene:2073, lld:C0009207;
    a sio:SIO_001121 .
}

dgn-np:NP309045.RAVwHhjTzVtE2JAfqZFIWZVZPy-rvA6Box9us5zLR4YGU130_provenance {
  dgn-np:NP309045.RAVwHhjTzVtE2JAfqZFIWZVZPy-rvA6Box9us5zLR4YGU130_assertion dcterms:description
      "[Cockayne syndrome (CS) cells and xeroderma pigmentosum (XP) cells (XPD, XPA, XPG, and XPF) were defective in Pol II degradation, whereas XPC cells whose defect is limited to global genome NER in nontranscribing regions were proficient for Pol II degradation.]. 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:18927284;
    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:NP309045.RAVwHhjTzVtE2JAfqZFIWZVZPy-rvA6Box9us5zLR4YGU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:57+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" .
}