@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP389654.RAYrp8O9D-ogelgz0wDCE6LSol2m_PSztTG6rEmDBoBIY> .
@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:NP389654.RAYrp8O9D-ogelgz0wDCE6LSol2m_PSztTG6rEmDBoBIY130_head {
  this: np:hasAssertion dgn-np:NP389654.RAYrp8O9D-ogelgz0wDCE6LSol2m_PSztTG6rEmDBoBIY130_assertion;
    np:hasProvenance dgn-np:NP389654.RAYrp8O9D-ogelgz0wDCE6LSol2m_PSztTG6rEmDBoBIY130_provenance;
    np:hasPublicationInfo dgn-np:NP389654.RAYrp8O9D-ogelgz0wDCE6LSol2m_PSztTG6rEmDBoBIY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP389654.RAYrp8O9D-ogelgz0wDCE6LSol2m_PSztTG6rEmDBoBIY130_assertion a np:Assertion .
  
  dgn-np:NP389654.RAYrp8O9D-ogelgz0wDCE6LSol2m_PSztTG6rEmDBoBIY130_provenance a np:Provenance .
  
  dgn-np:NP389654.RAYrp8O9D-ogelgz0wDCE6LSol2m_PSztTG6rEmDBoBIY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP389654.RAYrp8O9D-ogelgz0wDCE6LSol2m_PSztTG6rEmDBoBIY130_assertion {
  miriam-gene:472 a ncit:C16612 .
  
  lld:C0026986 a ncit:C7057 .
  
  dgn-gda:DGNf928954233080cd7ba89057c7546d75c sio:SIO_000628 miriam-gene:472, lld:C0026986;
    a sio:SIO_001121 .
}

dgn-np:NP389654.RAYrp8O9D-ogelgz0wDCE6LSol2m_PSztTG6rEmDBoBIY130_provenance {
  dgn-np:NP389654.RAYrp8O9D-ogelgz0wDCE6LSol2m_PSztTG6rEmDBoBIY130_assertion dcterms:description
      "[In conclusion, we demonstrate the heterogeneity of the DDR response in MDS and AML and provide evidence for its selective suppression in AML because of the uncoupling between activated ATM and inactive checkpoint kinases.]. 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:19398952;
    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:NP389654.RAYrp8O9D-ogelgz0wDCE6LSol2m_PSztTG6rEmDBoBIY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:52+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" .
}