@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP216134.RAIQMjX83A8UscDKSlrR6MANopsaBSMPe4khi6Q9GUjv4> .
@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:NP216134.RAIQMjX83A8UscDKSlrR6MANopsaBSMPe4khi6Q9GUjv4130_head {
  this: np:hasAssertion dgn-np:NP216134.RAIQMjX83A8UscDKSlrR6MANopsaBSMPe4khi6Q9GUjv4130_assertion;
    np:hasProvenance dgn-np:NP216134.RAIQMjX83A8UscDKSlrR6MANopsaBSMPe4khi6Q9GUjv4130_provenance;
    np:hasPublicationInfo dgn-np:NP216134.RAIQMjX83A8UscDKSlrR6MANopsaBSMPe4khi6Q9GUjv4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP216134.RAIQMjX83A8UscDKSlrR6MANopsaBSMPe4khi6Q9GUjv4130_assertion a np:Assertion .
  
  dgn-np:NP216134.RAIQMjX83A8UscDKSlrR6MANopsaBSMPe4khi6Q9GUjv4130_provenance a np:Provenance .
  
  dgn-np:NP216134.RAIQMjX83A8UscDKSlrR6MANopsaBSMPe4khi6Q9GUjv4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP216134.RAIQMjX83A8UscDKSlrR6MANopsaBSMPe4khi6Q9GUjv4130_assertion {
  miriam-gene:84106 a ncit:C16612 .
  
  lld:C0023487 a ncit:C7057 .
  
  dgn-gda:DGNdbe43e849934cf58b2028682c0e99d92 sio:SIO_000628 miriam-gene:84106, lld:C0023487;
    a sio:SIO_001121 .
}

dgn-np:NP216134.RAIQMjX83A8UscDKSlrR6MANopsaBSMPe4khi6Q9GUjv4130_provenance {
  dgn-np:NP216134.RAIQMjX83A8UscDKSlrR6MANopsaBSMPe4khi6Q9GUjv4130_assertion dcterms:description
      "[Some APL cases also involve rearrangements that fuse RAR to partner genes other than PML, including nucleophosmin (NPM), promyelocytic leukemia zinc finger (PLZF), nuclear mitotic apparatus (NUMA), and Stat5b, but the clinical characteristics of APL without PML-RAR have not been fully clarified.]. 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:17988991;
    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:NP216134.RAIQMjX83A8UscDKSlrR6MANopsaBSMPe4khi6Q9GUjv4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:00+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" .
}