@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP457695.RAB1bmSh8BVpUJ9hNf2v69WfCj8FpkJ33tl8POohBXNEQ> .
@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/v4.0.0/void/> .

dgn-np:NP457695.RAB1bmSh8BVpUJ9hNf2v69WfCj8FpkJ33tl8POohBXNEQ130_head {
  this: np:hasAssertion dgn-np:NP457695.RAB1bmSh8BVpUJ9hNf2v69WfCj8FpkJ33tl8POohBXNEQ130_assertion;
    np:hasProvenance dgn-np:NP457695.RAB1bmSh8BVpUJ9hNf2v69WfCj8FpkJ33tl8POohBXNEQ130_provenance;
    np:hasPublicationInfo dgn-np:NP457695.RAB1bmSh8BVpUJ9hNf2v69WfCj8FpkJ33tl8POohBXNEQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP457695.RAB1bmSh8BVpUJ9hNf2v69WfCj8FpkJ33tl8POohBXNEQ130_assertion a np:Assertion .
  
  dgn-np:NP457695.RAB1bmSh8BVpUJ9hNf2v69WfCj8FpkJ33tl8POohBXNEQ130_provenance a np:Provenance .
  
  dgn-np:NP457695.RAB1bmSh8BVpUJ9hNf2v69WfCj8FpkJ33tl8POohBXNEQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP457695.RAB1bmSh8BVpUJ9hNf2v69WfCj8FpkJ33tl8POohBXNEQ130_assertion {
  miriam-gene:26013 a ncit:C16612 .
  
  lld:C0376545 a ncit:C7057 .
  
  dgn-gda:DGN2b3f0a0627081602b3d4691378cfd79a sio:SIO_000628 miriam-gene:26013, lld:C0376545;
    a sio:SIO_001121 .
}

dgn-np:NP457695.RAB1bmSh8BVpUJ9hNf2v69WfCj8FpkJ33tl8POohBXNEQ130_provenance {
  dgn-np:NP457695.RAB1bmSh8BVpUJ9hNf2v69WfCj8FpkJ33tl8POohBXNEQ130_assertion dcterms:description
      "[To examine whether L3MBTL functions as a classic TSG in human hematologic malignancies, we screened a panel of 17 myeloid leukemia cell lines and peripheral blood or bone marrow samples from 29 MDS and 13 MPD patients for mutations in the entire L3MBTL coding sequence, including intron/exon splice junctions.]. 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:15334543;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP457695.RAB1bmSh8BVpUJ9hNf2v69WfCj8FpkJ33tl8POohBXNEQ130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:12+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}