@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP245155.RAD_w5fYzO0jn3e4MHS-vOIhm8vWp6KiKCTY4WM4o8mwM> .
@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:NP245155.RAD_w5fYzO0jn3e4MHS-vOIhm8vWp6KiKCTY4WM4o8mwM130_head {
  this: np:hasAssertion dgn-np:NP245155.RAD_w5fYzO0jn3e4MHS-vOIhm8vWp6KiKCTY4WM4o8mwM130_assertion;
    np:hasProvenance dgn-np:NP245155.RAD_w5fYzO0jn3e4MHS-vOIhm8vWp6KiKCTY4WM4o8mwM130_provenance;
    np:hasPublicationInfo dgn-np:NP245155.RAD_w5fYzO0jn3e4MHS-vOIhm8vWp6KiKCTY4WM4o8mwM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP245155.RAD_w5fYzO0jn3e4MHS-vOIhm8vWp6KiKCTY4WM4o8mwM130_assertion a np:Assertion .
  
  dgn-np:NP245155.RAD_w5fYzO0jn3e4MHS-vOIhm8vWp6KiKCTY4WM4o8mwM130_provenance a np:Provenance .
  
  dgn-np:NP245155.RAD_w5fYzO0jn3e4MHS-vOIhm8vWp6KiKCTY4WM4o8mwM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP245155.RAD_w5fYzO0jn3e4MHS-vOIhm8vWp6KiKCTY4WM4o8mwM130_assertion {
  miriam-gene:3342 a ncit:C16612 .
  
  lld:C0795878 a ncit:C7057 .
  
  dgn-gda:DGN51353e551c2603848ce26b58d78a2059 sio:SIO_000628 miriam-gene:3342, lld:C0795878;
    a sio:SIO_001121 .
}

dgn-np:NP245155.RAD_w5fYzO0jn3e4MHS-vOIhm8vWp6KiKCTY4WM4o8mwM130_provenance {
  dgn-np:NP245155.RAD_w5fYzO0jn3e4MHS-vOIhm8vWp6KiKCTY4WM4o8mwM130_assertion dcterms:description
      "[While comparative genomic hybridization (CGH) analysis identified monosomy 22 as the predominant change in RIM, occurring in frequencies comparable to those found in spontaneous meningioma (SM), molecular genetic analysis shows infrequent loss of chromosome 22 DNA markers.]. 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:12810249;
    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:NP245155.RAD_w5fYzO0jn3e4MHS-vOIhm8vWp6KiKCTY4WM4o8mwM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:17+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" .
}