@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP246556.RAiruuqpPTopauBelhQuCzOInWvr-Ns2tspXOm1LMTHN4> .
@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:NP246556.RAiruuqpPTopauBelhQuCzOInWvr-Ns2tspXOm1LMTHN4130_head {
  this: np:hasAssertion dgn-np:NP246556.RAiruuqpPTopauBelhQuCzOInWvr-Ns2tspXOm1LMTHN4130_assertion;
    np:hasProvenance dgn-np:NP246556.RAiruuqpPTopauBelhQuCzOInWvr-Ns2tspXOm1LMTHN4130_provenance;
    np:hasPublicationInfo dgn-np:NP246556.RAiruuqpPTopauBelhQuCzOInWvr-Ns2tspXOm1LMTHN4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP246556.RAiruuqpPTopauBelhQuCzOInWvr-Ns2tspXOm1LMTHN4130_assertion a np:Assertion .
  
  dgn-np:NP246556.RAiruuqpPTopauBelhQuCzOInWvr-Ns2tspXOm1LMTHN4130_provenance a np:Provenance .
  
  dgn-np:NP246556.RAiruuqpPTopauBelhQuCzOInWvr-Ns2tspXOm1LMTHN4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP246556.RAiruuqpPTopauBelhQuCzOInWvr-Ns2tspXOm1LMTHN4130_assertion {
  miriam-gene:7263 a ncit:C16612 .
  
  lld:C0000768 a ncit:C7057 .
  
  dgn-gda:DGN0779ddb84d75627c67222173bfa0208a sio:SIO_000628 miriam-gene:7263, lld:C0000768;
    a sio:SIO_001121 .
}

dgn-np:NP246556.RAiruuqpPTopauBelhQuCzOInWvr-Ns2tspXOm1LMTHN4130_provenance {
  dgn-np:NP246556.RAiruuqpPTopauBelhQuCzOInWvr-Ns2tspXOm1LMTHN4130_assertion dcterms:description
      "[Contrasting with the absence of any developmental abnormality, biological analyses revealed defects similar to those observed in NBS patients, including chromosomal instability, cellular hyperradiosensitivity and checkpoint defects as measured by radioresistant DNA synthesis (RDS).]. 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:19105185;
    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:NP246556.RAiruuqpPTopauBelhQuCzOInWvr-Ns2tspXOm1LMTHN4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:18+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" .
}