@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP713077.RAzs3i9nR4XXAzRYnVXxPCnfUqw4IA-wg9dZsJKQBlwWI> .
@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:NP713077.RAzs3i9nR4XXAzRYnVXxPCnfUqw4IA-wg9dZsJKQBlwWI130_head {
  this: np:hasAssertion dgn-np:NP713077.RAzs3i9nR4XXAzRYnVXxPCnfUqw4IA-wg9dZsJKQBlwWI130_assertion;
    np:hasProvenance dgn-np:NP713077.RAzs3i9nR4XXAzRYnVXxPCnfUqw4IA-wg9dZsJKQBlwWI130_provenance;
    np:hasPublicationInfo dgn-np:NP713077.RAzs3i9nR4XXAzRYnVXxPCnfUqw4IA-wg9dZsJKQBlwWI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP713077.RAzs3i9nR4XXAzRYnVXxPCnfUqw4IA-wg9dZsJKQBlwWI130_assertion a np:Assertion .
  
  dgn-np:NP713077.RAzs3i9nR4XXAzRYnVXxPCnfUqw4IA-wg9dZsJKQBlwWI130_provenance a np:Provenance .
  
  dgn-np:NP713077.RAzs3i9nR4XXAzRYnVXxPCnfUqw4IA-wg9dZsJKQBlwWI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP713077.RAzs3i9nR4XXAzRYnVXxPCnfUqw4IA-wg9dZsJKQBlwWI130_assertion {
  miriam-gene:2120 a ncit:C16612 .
  
  lld:C0004135 a ncit:C7057 .
  
  dgn-gda:DGNb816110c7dad48e9aa23d094879e1e8c sio:SIO_000628 miriam-gene:2120, lld:C0004135;
    a sio:SIO_001121 .
}

dgn-np:NP713077.RAzs3i9nR4XXAzRYnVXxPCnfUqw4IA-wg9dZsJKQBlwWI130_provenance {
  dgn-np:NP713077.RAzs3i9nR4XXAzRYnVXxPCnfUqw4IA-wg9dZsJKQBlwWI130_assertion dcterms:description
      "[Because of the homology of the human ATM gene to the TEL1 and rad3 genes of yeast, it has been suggested that mutations in ATM could lead to defective telomere maintenance.]. 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:10931683;
    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:NP713077.RAzs3i9nR4XXAzRYnVXxPCnfUqw4IA-wg9dZsJKQBlwWI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:13+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" .
}