@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP409309.RAZM8JwX-3urUbnLPcdNqP6pdCAiyZxFUrT53FmPVEVNg> .
@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:NP409309.RAZM8JwX-3urUbnLPcdNqP6pdCAiyZxFUrT53FmPVEVNg130_head {
  this: np:hasAssertion dgn-np:NP409309.RAZM8JwX-3urUbnLPcdNqP6pdCAiyZxFUrT53FmPVEVNg130_assertion;
    np:hasProvenance dgn-np:NP409309.RAZM8JwX-3urUbnLPcdNqP6pdCAiyZxFUrT53FmPVEVNg130_provenance;
    np:hasPublicationInfo dgn-np:NP409309.RAZM8JwX-3urUbnLPcdNqP6pdCAiyZxFUrT53FmPVEVNg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP409309.RAZM8JwX-3urUbnLPcdNqP6pdCAiyZxFUrT53FmPVEVNg130_assertion a np:Assertion .
  
  dgn-np:NP409309.RAZM8JwX-3urUbnLPcdNqP6pdCAiyZxFUrT53FmPVEVNg130_provenance a np:Provenance .
  
  dgn-np:NP409309.RAZM8JwX-3urUbnLPcdNqP6pdCAiyZxFUrT53FmPVEVNg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP409309.RAZM8JwX-3urUbnLPcdNqP6pdCAiyZxFUrT53FmPVEVNg130_assertion {
  miriam-gene:545 a ncit:C16612 .
  
  lld:C0149678 a ncit:C7057 .
  
  dgn-gda:DGN0b787ed4eab32eaccfae92f16bd8775b sio:SIO_000628 miriam-gene:545, lld:C0149678;
    a sio:SIO_001121 .
}

dgn-np:NP409309.RAZM8JwX-3urUbnLPcdNqP6pdCAiyZxFUrT53FmPVEVNg130_provenance {
  dgn-np:NP409309.RAZM8JwX-3urUbnLPcdNqP6pdCAiyZxFUrT53FmPVEVNg130_assertion dcterms:description
      "[To evaluate the role of ATR gene alterations in the pathogenesis of NKTCL and CAEBV, the whole coding region of the ATR gene was examined in cell lines derived from NKTCL and CAEBV, as well as tumor samples from patients.]. 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:16827800;
    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:NP409309.RAZM8JwX-3urUbnLPcdNqP6pdCAiyZxFUrT53FmPVEVNg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:03+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" .
}