@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP523029.RAqcvBOY1l8hpb6uE_cf4ijYt6AWSxB5r0SbZUCmqJ9Tk> .
@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:NP523029.RAqcvBOY1l8hpb6uE_cf4ijYt6AWSxB5r0SbZUCmqJ9Tk130_head {
  this: np:hasAssertion dgn-np:NP523029.RAqcvBOY1l8hpb6uE_cf4ijYt6AWSxB5r0SbZUCmqJ9Tk130_assertion;
    np:hasProvenance dgn-np:NP523029.RAqcvBOY1l8hpb6uE_cf4ijYt6AWSxB5r0SbZUCmqJ9Tk130_provenance;
    np:hasPublicationInfo dgn-np:NP523029.RAqcvBOY1l8hpb6uE_cf4ijYt6AWSxB5r0SbZUCmqJ9Tk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP523029.RAqcvBOY1l8hpb6uE_cf4ijYt6AWSxB5r0SbZUCmqJ9Tk130_assertion a np:Assertion .
  
  dgn-np:NP523029.RAqcvBOY1l8hpb6uE_cf4ijYt6AWSxB5r0SbZUCmqJ9Tk130_provenance a np:Provenance .
  
  dgn-np:NP523029.RAqcvBOY1l8hpb6uE_cf4ijYt6AWSxB5r0SbZUCmqJ9Tk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP523029.RAqcvBOY1l8hpb6uE_cf4ijYt6AWSxB5r0SbZUCmqJ9Tk130_assertion {
  miriam-gene:4771 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGN93ced5110c3e814914acd977fdd8309f sio:SIO_000628 miriam-gene:4771, lld:C0006826;
    a sio:SIO_001121 .
}

dgn-np:NP523029.RAqcvBOY1l8hpb6uE_cf4ijYt6AWSxB5r0SbZUCmqJ9Tk130_provenance {
  dgn-np:NP523029.RAqcvBOY1l8hpb6uE_cf4ijYt6AWSxB5r0SbZUCmqJ9Tk130_assertion dcterms:description
      "[Mutations of the neurofibromatosis 2 (NF2) tumor suppressor gene have frequently been detected not only in schwannomas and other central nervous system tumors of NF2 patients but also in their sporadic counterparts and malignant tumors unrelated to the NF2 syndrome such as malignant mesothelioma, indicating a broader role for the NF2 gene in human tumorigenesis.]. 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:17210637;
    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:NP523029.RAqcvBOY1l8hpb6uE_cf4ijYt6AWSxB5r0SbZUCmqJ9Tk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:11+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" .
}