@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP690044.RA4CjcpUVLR9nNnSt_DsCUinrgZPsLPZLxLBgkP_ECbvc> .
@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:NP690044.RA4CjcpUVLR9nNnSt_DsCUinrgZPsLPZLxLBgkP_ECbvc130_head {
  this: np:hasAssertion dgn-np:NP690044.RA4CjcpUVLR9nNnSt_DsCUinrgZPsLPZLxLBgkP_ECbvc130_assertion;
    np:hasProvenance dgn-np:NP690044.RA4CjcpUVLR9nNnSt_DsCUinrgZPsLPZLxLBgkP_ECbvc130_provenance;
    np:hasPublicationInfo dgn-np:NP690044.RA4CjcpUVLR9nNnSt_DsCUinrgZPsLPZLxLBgkP_ECbvc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP690044.RA4CjcpUVLR9nNnSt_DsCUinrgZPsLPZLxLBgkP_ECbvc130_assertion a np:Assertion .
  
  dgn-np:NP690044.RA4CjcpUVLR9nNnSt_DsCUinrgZPsLPZLxLBgkP_ECbvc130_provenance a np:Provenance .
  
  dgn-np:NP690044.RA4CjcpUVLR9nNnSt_DsCUinrgZPsLPZLxLBgkP_ECbvc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP690044.RA4CjcpUVLR9nNnSt_DsCUinrgZPsLPZLxLBgkP_ECbvc130_assertion {
  miriam-gene:545 a ncit:C16612 .
  
  lld:C0004135 a ncit:C7057 .
  
  dgn-gda:DGN865f86066f49a7fd229f086cca84132c sio:SIO_000628 miriam-gene:545, lld:C0004135;
    a sio:SIO_001121 .
}

dgn-np:NP690044.RA4CjcpUVLR9nNnSt_DsCUinrgZPsLPZLxLBgkP_ECbvc130_provenance {
  dgn-np:NP690044.RA4CjcpUVLR9nNnSt_DsCUinrgZPsLPZLxLBgkP_ECbvc130_assertion dcterms:description
      "[Based on the homology of the human ATM gene to the TEL1, MEC1 and rad3 genes of yeast, it has now been demonstrated that mutations in ATM lead to defective telomere maintenance in mammalian cells.]. 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:11850786;
    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:NP690044.RA4CjcpUVLR9nNnSt_DsCUinrgZPsLPZLxLBgkP_ECbvc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:59+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" .
}