@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP198712.RA6JUHeYc1hWNOqEBLipj6ySE6T2pEFa5_O6iGmyfZDsk> .
@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:NP198712.RA6JUHeYc1hWNOqEBLipj6ySE6T2pEFa5_O6iGmyfZDsk130_head {
   this: np:hasAssertion dgn-np:NP198712.RA6JUHeYc1hWNOqEBLipj6ySE6T2pEFa5_O6iGmyfZDsk130_assertion ;
    np:hasProvenance dgn-np:NP198712.RA6JUHeYc1hWNOqEBLipj6ySE6T2pEFa5_O6iGmyfZDsk130_provenance ;
    np:hasPublicationInfo dgn-np:NP198712.RA6JUHeYc1hWNOqEBLipj6ySE6T2pEFa5_O6iGmyfZDsk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP198712.RA6JUHeYc1hWNOqEBLipj6ySE6T2pEFa5_O6iGmyfZDsk130_assertion a np:Assertion .
  dgn-np:NP198712.RA6JUHeYc1hWNOqEBLipj6ySE6T2pEFa5_O6iGmyfZDsk130_provenance a np:Provenance .
  dgn-np:NP198712.RA6JUHeYc1hWNOqEBLipj6ySE6T2pEFa5_O6iGmyfZDsk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP198712.RA6JUHeYc1hWNOqEBLipj6ySE6T2pEFa5_O6iGmyfZDsk130_assertion {
   miriam-gene:7157 a ncit:C16612 .
  lld:C0028945 a ncit:C7057 .
  dgn-gda:DGNbad390f0e62e7a09a8e6a76213601948 sio:SIO_000628 miriam-gene:7157 , lld:C0028945 ;
    a sio:SIO_001121 .
}
dgn-np:NP198712.RA6JUHeYc1hWNOqEBLipj6ySE6T2pEFa5_O6iGmyfZDsk130_provenance {
   dgn-np:NP198712.RA6JUHeYc1hWNOqEBLipj6ySE6T2pEFa5_O6iGmyfZDsk130_assertion dcterms:description "[The study analysed INA, nestin, Olig2 and p53 expression, loss of heterozygosity of microsatellite markers from telomere to centromere of 10p, 10q, 1p and 19q chromosomes and epidermal growth factor receptor gene (EGFR) amplification in 40 gliomas (five astrocytomas, 12 oligodendrogliomas, 11 oligoastrocytomas, 12 glioblastomas).]. 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:21653654 ;
    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:NP198712.RA6JUHeYc1hWNOqEBLipj6ySE6T2pEFa5_O6iGmyfZDsk130_publicationInfo {
   this: dcterms:created "2014-10-02T12:33:49+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> ;
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}