@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP231216.RATHNpWsBIYRzGWe1ccGDKsuOpKjaaohxtki2KD2kGKso> .
@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:NP231216.RATHNpWsBIYRzGWe1ccGDKsuOpKjaaohxtki2KD2kGKso130_head {
  this: np:hasAssertion dgn-np:NP231216.RATHNpWsBIYRzGWe1ccGDKsuOpKjaaohxtki2KD2kGKso130_assertion;
    np:hasProvenance dgn-np:NP231216.RATHNpWsBIYRzGWe1ccGDKsuOpKjaaohxtki2KD2kGKso130_provenance;
    np:hasPublicationInfo dgn-np:NP231216.RATHNpWsBIYRzGWe1ccGDKsuOpKjaaohxtki2KD2kGKso130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP231216.RATHNpWsBIYRzGWe1ccGDKsuOpKjaaohxtki2KD2kGKso130_assertion a np:Assertion .
  
  dgn-np:NP231216.RATHNpWsBIYRzGWe1ccGDKsuOpKjaaohxtki2KD2kGKso130_provenance a np:Provenance .
  
  dgn-np:NP231216.RATHNpWsBIYRzGWe1ccGDKsuOpKjaaohxtki2KD2kGKso130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP231216.RATHNpWsBIYRzGWe1ccGDKsuOpKjaaohxtki2KD2kGKso130_assertion {
  miriam-gene:55655 a ncit:C16612 .
  
  lld:C0004135 a ncit:C7057 .
  
  dgn-gda:DGN2199ffbb60809e2d4fee2533ffb9444b sio:SIO_000628 miriam-gene:55655, lld:C0004135;
    a sio:SIO_001121 .
}

dgn-np:NP231216.RATHNpWsBIYRzGWe1ccGDKsuOpKjaaohxtki2KD2kGKso130_provenance {
  dgn-np:NP231216.RATHNpWsBIYRzGWe1ccGDKsuOpKjaaohxtki2KD2kGKso130_assertion dcterms:description
      "[Ataxia-Telangiectasia (A-T) and Nijmegen breakage syndrome (NBS) are recessive genetic diseases with similar cellular phenotypes that are caused by mutations in the recently described ATM (encoding ATM) and NBS1 (encoding p95) genes, respectively.]. 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:11981817;
    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:NP231216.RATHNpWsBIYRzGWe1ccGDKsuOpKjaaohxtki2KD2kGKso130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:09+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" .
}