@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1013927.RAnXoK0k-ACoymNWRlpEYJjhjy6eEf0x_6BhVobAq6XdU> .
@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:NP1013927.RAnXoK0k-ACoymNWRlpEYJjhjy6eEf0x_6BhVobAq6XdU130_head {
  this: np:hasAssertion dgn-np:NP1013927.RAnXoK0k-ACoymNWRlpEYJjhjy6eEf0x_6BhVobAq6XdU130_assertion;
    np:hasProvenance dgn-np:NP1013927.RAnXoK0k-ACoymNWRlpEYJjhjy6eEf0x_6BhVobAq6XdU130_provenance;
    np:hasPublicationInfo dgn-np:NP1013927.RAnXoK0k-ACoymNWRlpEYJjhjy6eEf0x_6BhVobAq6XdU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1013927.RAnXoK0k-ACoymNWRlpEYJjhjy6eEf0x_6BhVobAq6XdU130_assertion a np:Assertion .
  
  dgn-np:NP1013927.RAnXoK0k-ACoymNWRlpEYJjhjy6eEf0x_6BhVobAq6XdU130_provenance a np:Provenance .
  
  dgn-np:NP1013927.RAnXoK0k-ACoymNWRlpEYJjhjy6eEf0x_6BhVobAq6XdU130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1013927.RAnXoK0k-ACoymNWRlpEYJjhjy6eEf0x_6BhVobAq6XdU130_assertion {
  miriam-gene:100302736 a ncit:C16612 .
  
  lld:C0023493 a ncit:C7057 .
  
  dgn-gda:DGN21b44bbadf7c755b6e5617651f937e37 sio:SIO_000628 miriam-gene:100302736,
      lld:C0023493;
    a sio:SIO_001121 .
}

dgn-np:NP1013927.RAnXoK0k-ACoymNWRlpEYJjhjy6eEf0x_6BhVobAq6XdU130_provenance {
  dgn-np:NP1013927.RAnXoK0k-ACoymNWRlpEYJjhjy6eEf0x_6BhVobAq6XdU130_assertion dcterms:description
      "[Although genetic alterations of p18, p19, p21, p27 have rarely been reported, inactivation of these genes may contribute to the development of ATLL because low expression levels of these genes seem to mark ATLL.]. 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:12040438;
    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:NP1013927.RAnXoK0k-ACoymNWRlpEYJjhjy6eEf0x_6BhVobAq6XdU130_publicationInfo {
  this: dcterms:created "2015-08-25T14:48:09+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" .
}