@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP499431.RABnoBTBIoEBdLIL2dRGge_f5UqptO-NP2lrrqscjqccA> .
@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:NP499431.RABnoBTBIoEBdLIL2dRGge_f5UqptO-NP2lrrqscjqccA130_head {
  this: np:hasAssertion dgn-np:NP499431.RABnoBTBIoEBdLIL2dRGge_f5UqptO-NP2lrrqscjqccA130_assertion;
    np:hasProvenance dgn-np:NP499431.RABnoBTBIoEBdLIL2dRGge_f5UqptO-NP2lrrqscjqccA130_provenance;
    np:hasPublicationInfo dgn-np:NP499431.RABnoBTBIoEBdLIL2dRGge_f5UqptO-NP2lrrqscjqccA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP499431.RABnoBTBIoEBdLIL2dRGge_f5UqptO-NP2lrrqscjqccA130_assertion a np:Assertion .
  
  dgn-np:NP499431.RABnoBTBIoEBdLIL2dRGge_f5UqptO-NP2lrrqscjqccA130_provenance a np:Provenance .
  
  dgn-np:NP499431.RABnoBTBIoEBdLIL2dRGge_f5UqptO-NP2lrrqscjqccA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP499431.RABnoBTBIoEBdLIL2dRGge_f5UqptO-NP2lrrqscjqccA130_assertion {
  miriam-gene:6201 a ncit:C16612 .
  
  lld:C0398550 a ncit:C7057 .
  
  dgn-gda:DGNcbf6ba16b68ee11aad2b2f2cd7c40ba3 sio:SIO_000628 miriam-gene:6201, lld:C0398550;
    a sio:SIO_001121 .
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dgn-np:NP499431.RABnoBTBIoEBdLIL2dRGge_f5UqptO-NP2lrrqscjqccA130_provenance {
  dgn-np:NP499431.RABnoBTBIoEBdLIL2dRGge_f5UqptO-NP2lrrqscjqccA130_assertion dcterms:description
      "[We also demonstrate that mutations of RPL5, RPL11, or RPS7 in DBA cells is associated with diverse defects in the maturation of ribosomal RNAs in the large or the small ribosomal subunit production pathway, expanding the repertoire of ribosomal RNA processing defects associated with DBA.]. 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:19061985;
    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:NP499431.RABnoBTBIoEBdLIL2dRGge_f5UqptO-NP2lrrqscjqccA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:58+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>,
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    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}