@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP631546.RA-2LSWbDq6gB2bhLRuq0ngMX4BjdQPBwc3Z8KDuvXgj8> .
@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:NP631546.RA-2LSWbDq6gB2bhLRuq0ngMX4BjdQPBwc3Z8KDuvXgj8130_head {
  this: np:hasAssertion dgn-np:NP631546.RA-2LSWbDq6gB2bhLRuq0ngMX4BjdQPBwc3Z8KDuvXgj8130_assertion;
    np:hasProvenance dgn-np:NP631546.RA-2LSWbDq6gB2bhLRuq0ngMX4BjdQPBwc3Z8KDuvXgj8130_provenance;
    np:hasPublicationInfo dgn-np:NP631546.RA-2LSWbDq6gB2bhLRuq0ngMX4BjdQPBwc3Z8KDuvXgj8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP631546.RA-2LSWbDq6gB2bhLRuq0ngMX4BjdQPBwc3Z8KDuvXgj8130_assertion a np:Assertion .
  
  dgn-np:NP631546.RA-2LSWbDq6gB2bhLRuq0ngMX4BjdQPBwc3Z8KDuvXgj8130_provenance a np:Provenance .
  
  dgn-np:NP631546.RA-2LSWbDq6gB2bhLRuq0ngMX4BjdQPBwc3Z8KDuvXgj8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP631546.RA-2LSWbDq6gB2bhLRuq0ngMX4BjdQPBwc3Z8KDuvXgj8130_assertion {
  miriam-gene:6208 a ncit:C16612 .
  
  lld:C0002871 a ncit:C7057 .
  
  dgn-gda:DGN1daf95b869ce60414013f1023ee2abda sio:SIO_000628 miriam-gene:6208, lld:C0002871;
    a sio:SIO_001121 .
}

dgn-np:NP631546.RA-2LSWbDq6gB2bhLRuq0ngMX4BjdQPBwc3Z8KDuvXgj8130_provenance {
  dgn-np:NP631546.RA-2LSWbDq6gB2bhLRuq0ngMX4BjdQPBwc3Z8KDuvXgj8130_assertion dcterms:description
      "[Patients with nonclassical DBA and other hypoproliferative anemias may have somatically acquired 5q deletions with RPS14 haploinsufficiency not identified by fluorescence in situ hybridization or cytogenetic testing, thus refining the spectrum of disorders with 5q- deletions.]. 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:23943650;
    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:NP631546.RA-2LSWbDq6gB2bhLRuq0ngMX4BjdQPBwc3Z8KDuvXgj8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:21+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" .
}