@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP388333.RAzYlHRgh5RbmvA2qU9DcWWBgBC6dr4M59knr6pSKMcYQ> .
@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:NP388333.RAzYlHRgh5RbmvA2qU9DcWWBgBC6dr4M59knr6pSKMcYQ130_head {
  this: np:hasAssertion dgn-np:NP388333.RAzYlHRgh5RbmvA2qU9DcWWBgBC6dr4M59knr6pSKMcYQ130_assertion ;
    np:hasProvenance dgn-np:NP388333.RAzYlHRgh5RbmvA2qU9DcWWBgBC6dr4M59knr6pSKMcYQ130_provenance ;
    np:hasPublicationInfo dgn-np:NP388333.RAzYlHRgh5RbmvA2qU9DcWWBgBC6dr4M59knr6pSKMcYQ130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP388333.RAzYlHRgh5RbmvA2qU9DcWWBgBC6dr4M59knr6pSKMcYQ130_assertion a np:Assertion .
  dgn-np:NP388333.RAzYlHRgh5RbmvA2qU9DcWWBgBC6dr4M59knr6pSKMcYQ130_provenance a np:Provenance .
  dgn-np:NP388333.RAzYlHRgh5RbmvA2qU9DcWWBgBC6dr4M59knr6pSKMcYQ130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP388333.RAzYlHRgh5RbmvA2qU9DcWWBgBC6dr4M59knr6pSKMcYQ130_assertion {
  miriam-gene:4771 a ncit:C16612 .
  lld:C0017638 a ncit:C7057 .
  dgn-gda:DGNf0c0c52fedac32605a36752c021d726a sio:SIO_000628 miriam-gene:4771 , lld:C0017638 ;
    a sio:SIO_001121 .
}
dgn-np:NP388333.RAzYlHRgh5RbmvA2qU9DcWWBgBC6dr4M59knr6pSKMcYQ130_provenance {
  dgn-np:NP388333.RAzYlHRgh5RbmvA2qU9DcWWBgBC6dr4M59knr6pSKMcYQ130_assertion dcterms:description "[Thus, although frequent loss of heterozygosity on chromosome 22 suggests that inactivation of a tumor suppressor gene on this chromosome plays a role in development of gliomas, there is no evidence that inactivation of the NF2 gene is implicated in this process, confirming the results of other studies of the NF2 gene in human gliomas.]. 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:8956876 ;
    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:NP388333.RAzYlHRgh5RbmvA2qU9DcWWBgBC6dr4M59knr6pSKMcYQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:51+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" .
}