@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP786960.RA-wLLTT309TtNtzfnYFRCpz_JLvTZqUrGQl8FvE1WB6g> .
@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:NP786960.RA-wLLTT309TtNtzfnYFRCpz_JLvTZqUrGQl8FvE1WB6g130_head {
  this: np:hasAssertion dgn-np:NP786960.RA-wLLTT309TtNtzfnYFRCpz_JLvTZqUrGQl8FvE1WB6g130_assertion ;
    np:hasProvenance dgn-np:NP786960.RA-wLLTT309TtNtzfnYFRCpz_JLvTZqUrGQl8FvE1WB6g130_provenance ;
    np:hasPublicationInfo dgn-np:NP786960.RA-wLLTT309TtNtzfnYFRCpz_JLvTZqUrGQl8FvE1WB6g130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP786960.RA-wLLTT309TtNtzfnYFRCpz_JLvTZqUrGQl8FvE1WB6g130_assertion a np:Assertion .
  dgn-np:NP786960.RA-wLLTT309TtNtzfnYFRCpz_JLvTZqUrGQl8FvE1WB6g130_provenance a np:Provenance .
  dgn-np:NP786960.RA-wLLTT309TtNtzfnYFRCpz_JLvTZqUrGQl8FvE1WB6g130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP786960.RA-wLLTT309TtNtzfnYFRCpz_JLvTZqUrGQl8FvE1WB6g130_assertion {
  miriam-gene:4771 a ncit:C16612 .
  lld:C0006826 a ncit:C7057 .
  dgn-gda:DGN72a0df67296c02c256b6f5bfc311dcdc sio:SIO_000628 miriam-gene:4771 , lld:C0006826 ;
    a sio:SIO_001121 .
}
dgn-np:NP786960.RA-wLLTT309TtNtzfnYFRCpz_JLvTZqUrGQl8FvE1WB6g130_provenance {
  dgn-np:NP786960.RA-wLLTT309TtNtzfnYFRCpz_JLvTZqUrGQl8FvE1WB6g130_assertion dcterms:description "[As the molecular pathogenesis of meningiomas and schwannomas, characterized by NF2 gene alterations, remains unclear and suitable molecular targets need to be identified, we used low density cDNA microarrays to establish expression patterns of 96 cancer-related genes on 23 schwannomas, 42 meningiomas and 3 normal cerebral meninges.]. 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:19148485 ;
    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:NP786960.RA-wLLTT309TtNtzfnYFRCpz_JLvTZqUrGQl8FvE1WB6g130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:00+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" .
}