@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP630038.RA3kSKEROAZPt7dctBFO0SMfqvf2OU9wdcVmeZ2QKev5A> .
@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:NP630038.RA3kSKEROAZPt7dctBFO0SMfqvf2OU9wdcVmeZ2QKev5A130_head {
  this: np:hasAssertion dgn-np:NP630038.RA3kSKEROAZPt7dctBFO0SMfqvf2OU9wdcVmeZ2QKev5A130_assertion;
    np:hasProvenance dgn-np:NP630038.RA3kSKEROAZPt7dctBFO0SMfqvf2OU9wdcVmeZ2QKev5A130_provenance;
    np:hasPublicationInfo dgn-np:NP630038.RA3kSKEROAZPt7dctBFO0SMfqvf2OU9wdcVmeZ2QKev5A130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP630038.RA3kSKEROAZPt7dctBFO0SMfqvf2OU9wdcVmeZ2QKev5A130_assertion a np:Assertion .
  
  dgn-np:NP630038.RA3kSKEROAZPt7dctBFO0SMfqvf2OU9wdcVmeZ2QKev5A130_provenance a np:Provenance .
  
  dgn-np:NP630038.RA3kSKEROAZPt7dctBFO0SMfqvf2OU9wdcVmeZ2QKev5A130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP630038.RA3kSKEROAZPt7dctBFO0SMfqvf2OU9wdcVmeZ2QKev5A130_assertion {
  miriam-gene:730394 a ncit:C16612 .
  
  lld:C0740342 a ncit:C7057 .
  
  dgn-gda:DGN33ec16af7f3964c1fe11642aedeb17f8 sio:SIO_000628 miriam-gene:730394, lld:C0740342;
    a sio:SIO_001121 .
}

dgn-np:NP630038.RA3kSKEROAZPt7dctBFO0SMfqvf2OU9wdcVmeZ2QKev5A130_provenance {
  dgn-np:NP630038.RA3kSKEROAZPt7dctBFO0SMfqvf2OU9wdcVmeZ2QKev5A130_assertion dcterms:description
      "[The involvement of some if not all of the TFIIH subunits in transcription and repair may explain the heterogeneity of the various and sometimes completely unrelated symptoms observed in xeroderma pigmentosum, Cockayne Syndrome and trichothiodystrophy disorders.]. 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:7980491;
    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:NP630038.RA3kSKEROAZPt7dctBFO0SMfqvf2OU9wdcVmeZ2QKev5A130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:20+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" .
}