@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP603808.RAI8tn738_VYGKqeFmmwOe2C5eZHrBDR06OVxbFvjwzRA> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP603808.RAI8tn738_VYGKqeFmmwOe2C5eZHrBDR06OVxbFvjwzRA130_head {
  this: np:hasAssertion dgn-np:NP603808.RAI8tn738_VYGKqeFmmwOe2C5eZHrBDR06OVxbFvjwzRA130_assertion;
    np:hasProvenance dgn-np:NP603808.RAI8tn738_VYGKqeFmmwOe2C5eZHrBDR06OVxbFvjwzRA130_provenance;
    np:hasPublicationInfo dgn-np:NP603808.RAI8tn738_VYGKqeFmmwOe2C5eZHrBDR06OVxbFvjwzRA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP603808.RAI8tn738_VYGKqeFmmwOe2C5eZHrBDR06OVxbFvjwzRA130_assertion a np:Assertion .
  
  dgn-np:NP603808.RAI8tn738_VYGKqeFmmwOe2C5eZHrBDR06OVxbFvjwzRA130_provenance a np:Provenance .
  
  dgn-np:NP603808.RAI8tn738_VYGKqeFmmwOe2C5eZHrBDR06OVxbFvjwzRA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP603808.RAI8tn738_VYGKqeFmmwOe2C5eZHrBDR06OVxbFvjwzRA130_assertion {
  miriam-gene:5001 a ncit:C16612 .
  
  lld:C0026986 a ncit:C7057 .
  
  dgn-gda:DGNf53f7b210f27f3ff893b3363bc1bdcb4 sio:SIO_000628 miriam-gene:5001, lld:C0026986;
    a sio:SIO_001121 .
}

dgn-np:NP603808.RAI8tn738_VYGKqeFmmwOe2C5eZHrBDR06OVxbFvjwzRA130_provenance {
  dgn-np:NP603808.RAI8tn738_VYGKqeFmmwOe2C5eZHrBDR06OVxbFvjwzRA130_assertion dcterms:description
      "[Polymerase chain reaction amplification and sequencing analysis of the coding region of the remaining ORC5L allele has not revealed any mutations in nine patients with AML or MDS exhibiting 7q22 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:11379876;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP603808.RAI8tn738_VYGKqeFmmwOe2C5eZHrBDR06OVxbFvjwzRA130_publicationInfo {
  this: dcterms:created "2015-08-25T14:43:41+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}