@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1410938.RAP9h-aCSDYbT6ImhIukeQFr7evHrMVvFRzl-QUzZc0dg> .
@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:NP1410938.RAP9h-aCSDYbT6ImhIukeQFr7evHrMVvFRzl-QUzZc0dg130_head {
  this: np:hasAssertion dgn-np:NP1410938.RAP9h-aCSDYbT6ImhIukeQFr7evHrMVvFRzl-QUzZc0dg130_assertion;
    np:hasProvenance dgn-np:NP1410938.RAP9h-aCSDYbT6ImhIukeQFr7evHrMVvFRzl-QUzZc0dg130_provenance;
    np:hasPublicationInfo dgn-np:NP1410938.RAP9h-aCSDYbT6ImhIukeQFr7evHrMVvFRzl-QUzZc0dg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1410938.RAP9h-aCSDYbT6ImhIukeQFr7evHrMVvFRzl-QUzZc0dg130_assertion a np:Assertion .
  
  dgn-np:NP1410938.RAP9h-aCSDYbT6ImhIukeQFr7evHrMVvFRzl-QUzZc0dg130_provenance a np:Provenance .
  
  dgn-np:NP1410938.RAP9h-aCSDYbT6ImhIukeQFr7evHrMVvFRzl-QUzZc0dg130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1410938.RAP9h-aCSDYbT6ImhIukeQFr7evHrMVvFRzl-QUzZc0dg130_assertion {
  miriam-gene:4771 a ncit:C16612 .
  
  lld:C0025286 a ncit:C7057 .
  
  dgn-gda:DGN7a390f0e6e67cb2101e833d06844e5a5 sio:SIO_000628 miriam-gene:4771, lld:C0025286;
    a sio:SIO_001121 .
}

dgn-np:NP1410938.RAP9h-aCSDYbT6ImhIukeQFr7evHrMVvFRzl-QUzZc0dg130_provenance {
  dgn-np:NP1410938.RAP9h-aCSDYbT6ImhIukeQFr7evHrMVvFRzl-QUzZc0dg130_assertion dcterms:description
      "[We analysed 23 sporadic schwannomas for mutations in the NF2 gene and for the allelic status at 1p, 14q and 22q, as alterations of these genomic regions appear to be related to tumour progression in meningiomas, another NF2-associated neoplasm.]. 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:9852312;
    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:NP1410938.RAP9h-aCSDYbT6ImhIukeQFr7evHrMVvFRzl-QUzZc0dg130_publicationInfo {
  this: dcterms:created "2016-05-13T12:52:26+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" .
}