@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP552786.RAFUE9YtGi2fW3_x2zbdlZGfYa7E-PPq09WjMtyfpawZ8> .
@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:NP552786.RAFUE9YtGi2fW3_x2zbdlZGfYa7E-PPq09WjMtyfpawZ8130_head {
  this: np:hasAssertion dgn-np:NP552786.RAFUE9YtGi2fW3_x2zbdlZGfYa7E-PPq09WjMtyfpawZ8130_assertion;
    np:hasProvenance dgn-np:NP552786.RAFUE9YtGi2fW3_x2zbdlZGfYa7E-PPq09WjMtyfpawZ8130_provenance;
    np:hasPublicationInfo dgn-np:NP552786.RAFUE9YtGi2fW3_x2zbdlZGfYa7E-PPq09WjMtyfpawZ8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP552786.RAFUE9YtGi2fW3_x2zbdlZGfYa7E-PPq09WjMtyfpawZ8130_assertion a np:Assertion .
  
  dgn-np:NP552786.RAFUE9YtGi2fW3_x2zbdlZGfYa7E-PPq09WjMtyfpawZ8130_provenance a np:Provenance .
  
  dgn-np:NP552786.RAFUE9YtGi2fW3_x2zbdlZGfYa7E-PPq09WjMtyfpawZ8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP552786.RAFUE9YtGi2fW3_x2zbdlZGfYa7E-PPq09WjMtyfpawZ8130_assertion {
  miriam-gene:23512 a ncit:C16612 .
  
  lld:C0206728 a ncit:C7057 .
  
  dgn-gda:DGN15ad3d250712f608803c78cfa0c2acf2 sio:SIO_000628 miriam-gene:23512, lld:C0206728;
    a sio:SIO_001121 .
}

dgn-np:NP552786.RAFUE9YtGi2fW3_x2zbdlZGfYa7E-PPq09WjMtyfpawZ8130_provenance {
  dgn-np:NP552786.RAFUE9YtGi2fW3_x2zbdlZGfYa7E-PPq09WjMtyfpawZ8130_assertion dcterms:description
      "[Although somatic inactivation of the NF1 wild-type allele is considered to be the PNF-initiating event in NF1 patients with intragenic mutations and patients with NF1 microdeletions, both patient groups may differ with regard to tumour progression because of the heterozygous constitutional deletion of SUZ12 present only in patients with NF1 microdeletions.]. 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:23101500;
    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:NP552786.RAFUE9YtGi2fW3_x2zbdlZGfYa7E-PPq09WjMtyfpawZ8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:33+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" .
}