@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP471292.RAz3ZCeOA6kAdKxbYguA_Krx5bozy9ksERtpve2_cCpDA> .
@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:NP471292.RAz3ZCeOA6kAdKxbYguA_Krx5bozy9ksERtpve2_cCpDA130_head {
  this: np:hasAssertion dgn-np:NP471292.RAz3ZCeOA6kAdKxbYguA_Krx5bozy9ksERtpve2_cCpDA130_assertion;
    np:hasProvenance dgn-np:NP471292.RAz3ZCeOA6kAdKxbYguA_Krx5bozy9ksERtpve2_cCpDA130_provenance;
    np:hasPublicationInfo dgn-np:NP471292.RAz3ZCeOA6kAdKxbYguA_Krx5bozy9ksERtpve2_cCpDA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP471292.RAz3ZCeOA6kAdKxbYguA_Krx5bozy9ksERtpve2_cCpDA130_assertion a np:Assertion .
  
  dgn-np:NP471292.RAz3ZCeOA6kAdKxbYguA_Krx5bozy9ksERtpve2_cCpDA130_provenance a np:Provenance .
  
  dgn-np:NP471292.RAz3ZCeOA6kAdKxbYguA_Krx5bozy9ksERtpve2_cCpDA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP471292.RAz3ZCeOA6kAdKxbYguA_Krx5bozy9ksERtpve2_cCpDA130_assertion {
  miriam-gene:4771 a ncit:C16612 .
  
  lld:C0205834 a ncit:C7057 .
  
  dgn-gda:DGNf9e05896ce006d23e9b7ab032685a28f sio:SIO_000628 miriam-gene:4771, lld:C0205834;
    a sio:SIO_001121 .
}

dgn-np:NP471292.RAz3ZCeOA6kAdKxbYguA_Krx5bozy9ksERtpve2_cCpDA130_provenance {
  dgn-np:NP471292.RAz3ZCeOA6kAdKxbYguA_Krx5bozy9ksERtpve2_cCpDA130_assertion dcterms:description
      "[Most of these cases display NF2 gene mutations parallel to loss of the chromosome 22 homolog, indicating that inactivation of this gene may represent an early event in the development of multiple meningiomas.]. 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:11979381;
    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:NP471292.RAz3ZCeOA6kAdKxbYguA_Krx5bozy9ksERtpve2_cCpDA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:42+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" .
}