@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP568575.RA8v_LcM0B3tTbwWr3H5vWF6DFOpshjs3pN_Ke36vfL3o> .
@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:NP568575.RA8v_LcM0B3tTbwWr3H5vWF6DFOpshjs3pN_Ke36vfL3o130_head {
  this: np:hasAssertion dgn-np:NP568575.RA8v_LcM0B3tTbwWr3H5vWF6DFOpshjs3pN_Ke36vfL3o130_assertion;
    np:hasProvenance dgn-np:NP568575.RA8v_LcM0B3tTbwWr3H5vWF6DFOpshjs3pN_Ke36vfL3o130_provenance;
    np:hasPublicationInfo dgn-np:NP568575.RA8v_LcM0B3tTbwWr3H5vWF6DFOpshjs3pN_Ke36vfL3o130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP568575.RA8v_LcM0B3tTbwWr3H5vWF6DFOpshjs3pN_Ke36vfL3o130_assertion a np:Assertion .
  
  dgn-np:NP568575.RA8v_LcM0B3tTbwWr3H5vWF6DFOpshjs3pN_Ke36vfL3o130_provenance a np:Provenance .
  
  dgn-np:NP568575.RA8v_LcM0B3tTbwWr3H5vWF6DFOpshjs3pN_Ke36vfL3o130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP568575.RA8v_LcM0B3tTbwWr3H5vWF6DFOpshjs3pN_Ke36vfL3o130_assertion {
  miriam-gene:2272 a ncit:C16612 .
  
  lld:C0027708 a ncit:C7057 .
  
  dgn-gda:DGN567400dfee6d3f86ff03b18dd3dd0ae8 sio:SIO_000628 miriam-gene:2272, lld:C0027708;
    a sio:SIO_001121 .
}

dgn-np:NP568575.RA8v_LcM0B3tTbwWr3H5vWF6DFOpshjs3pN_Ke36vfL3o130_provenance {
  dgn-np:NP568575.RA8v_LcM0B3tTbwWr3H5vWF6DFOpshjs3pN_Ke36vfL3o130_assertion dcterms:description
      "[The majority of chromosomes displayed uniparental disomies, and microdeletions were present in genes with known importance for tumor formation (LRP1B, FHIT, and WWOX) or organogenesis (NEGR1 and ZFPM2), abnormalities not previously reported for pediatric WT.]. 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:21947875;
    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:NP568575.RA8v_LcM0B3tTbwWr3H5vWF6DFOpshjs3pN_Ke36vfL3o130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:43+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" .
}