@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP720753.RAsMPTGmgzihLrQl-a5tg2EHNmHhICzOGnD6yhbsB6ffY> .
@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:NP720753.RAsMPTGmgzihLrQl-a5tg2EHNmHhICzOGnD6yhbsB6ffY130_head {
  this: np:hasAssertion dgn-np:NP720753.RAsMPTGmgzihLrQl-a5tg2EHNmHhICzOGnD6yhbsB6ffY130_assertion;
    np:hasProvenance dgn-np:NP720753.RAsMPTGmgzihLrQl-a5tg2EHNmHhICzOGnD6yhbsB6ffY130_provenance;
    np:hasPublicationInfo dgn-np:NP720753.RAsMPTGmgzihLrQl-a5tg2EHNmHhICzOGnD6yhbsB6ffY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP720753.RAsMPTGmgzihLrQl-a5tg2EHNmHhICzOGnD6yhbsB6ffY130_assertion a np:Assertion .
  
  dgn-np:NP720753.RAsMPTGmgzihLrQl-a5tg2EHNmHhICzOGnD6yhbsB6ffY130_provenance a np:Provenance .
  
  dgn-np:NP720753.RAsMPTGmgzihLrQl-a5tg2EHNmHhICzOGnD6yhbsB6ffY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP720753.RAsMPTGmgzihLrQl-a5tg2EHNmHhICzOGnD6yhbsB6ffY130_assertion {
  miriam-gene:4771 a ncit:C16612 .
  
  lld:C0026499 a ncit:C7057 .
  
  dgn-gda:DGN4f29b3bea1674ff581d0aba4418313a6 sio:SIO_000628 miriam-gene:4771, lld:C0026499;
    a sio:SIO_001121 .
}

dgn-np:NP720753.RAsMPTGmgzihLrQl-a5tg2EHNmHhICzOGnD6yhbsB6ffY130_provenance {
  dgn-np:NP720753.RAsMPTGmgzihLrQl-a5tg2EHNmHhICzOGnD6yhbsB6ffY130_assertion dcterms:description
      "[Fluorescence in situ hybridization studies performed with probes targeting the NF2 gene and other members of the protein 4.1 gene family demonstrated similar alterations in the ependymal and sarcomatous components in the cases tested, including polysomies/polyploidy (n=3), gains of 1q (n=3), deletions of 22q (n=2) and 6q (n=1), and monosomy 18 (n=1).]. 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:18347506;
    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:NP720753.RAsMPTGmgzihLrQl-a5tg2EHNmHhICzOGnD6yhbsB6ffY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:17+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" .
}