@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP818413.RAc78c8PQ1Jbs2znMaIRbr3qHr45pQxNeLtgvKVQ-zELE> .
@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:NP818413.RAc78c8PQ1Jbs2znMaIRbr3qHr45pQxNeLtgvKVQ-zELE130_head {
  this: np:hasAssertion dgn-np:NP818413.RAc78c8PQ1Jbs2znMaIRbr3qHr45pQxNeLtgvKVQ-zELE130_assertion;
    np:hasProvenance dgn-np:NP818413.RAc78c8PQ1Jbs2znMaIRbr3qHr45pQxNeLtgvKVQ-zELE130_provenance;
    np:hasPublicationInfo dgn-np:NP818413.RAc78c8PQ1Jbs2znMaIRbr3qHr45pQxNeLtgvKVQ-zELE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP818413.RAc78c8PQ1Jbs2znMaIRbr3qHr45pQxNeLtgvKVQ-zELE130_assertion a np:Assertion .
  
  dgn-np:NP818413.RAc78c8PQ1Jbs2znMaIRbr3qHr45pQxNeLtgvKVQ-zELE130_provenance a np:Provenance .
  
  dgn-np:NP818413.RAc78c8PQ1Jbs2znMaIRbr3qHr45pQxNeLtgvKVQ-zELE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP818413.RAc78c8PQ1Jbs2znMaIRbr3qHr45pQxNeLtgvKVQ-zELE130_assertion {
  miriam-gene:2272 a ncit:C16612 .
  
  lld:C0006079 a ncit:C7057 .
  
  dgn-gda:DGN5aca94f7f1e5ece9d8206bb624988043 sio:SIO_000628 miriam-gene:2272, lld:C0006079;
    a sio:SIO_001121 .
}

dgn-np:NP818413.RAc78c8PQ1Jbs2znMaIRbr3qHr45pQxNeLtgvKVQ-zELE130_provenance {
  dgn-np:NP818413.RAc78c8PQ1Jbs2znMaIRbr3qHr45pQxNeLtgvKVQ-zELE130_assertion dcterms:description
      "[To evaluate the role of the Fragile Histidine Triad gene in nonmelanoma skin cancer, we have used reverse transcriptase polymerase chain reaction analysis to screen for deletions in 16 tumors (five basal cell carcinomas, five squamous cell carcinomas, five actinic keratoses, and one case of Bowen's disease) and HaCaT and A431 cell lines.]. 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:9406824;
    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:NP818413.RAc78c8PQ1Jbs2znMaIRbr3qHr45pQxNeLtgvKVQ-zELE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:21+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" .
}