@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP425159.RAlhWKQbSKKwK9S06bTpYV3_RcMPDEwNw3-AN-lNEqCN0> .
@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:NP425159.RAlhWKQbSKKwK9S06bTpYV3_RcMPDEwNw3-AN-lNEqCN0130_head {
  this: np:hasAssertion dgn-np:NP425159.RAlhWKQbSKKwK9S06bTpYV3_RcMPDEwNw3-AN-lNEqCN0130_assertion ;
    np:hasProvenance dgn-np:NP425159.RAlhWKQbSKKwK9S06bTpYV3_RcMPDEwNw3-AN-lNEqCN0130_provenance ;
    np:hasPublicationInfo dgn-np:NP425159.RAlhWKQbSKKwK9S06bTpYV3_RcMPDEwNw3-AN-lNEqCN0130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP425159.RAlhWKQbSKKwK9S06bTpYV3_RcMPDEwNw3-AN-lNEqCN0130_assertion a np:Assertion .
  dgn-np:NP425159.RAlhWKQbSKKwK9S06bTpYV3_RcMPDEwNw3-AN-lNEqCN0130_provenance a np:Provenance .
  dgn-np:NP425159.RAlhWKQbSKKwK9S06bTpYV3_RcMPDEwNw3-AN-lNEqCN0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP425159.RAlhWKQbSKKwK9S06bTpYV3_RcMPDEwNw3-AN-lNEqCN0130_assertion {
  miriam-gene:1019 a ncit:C16612 .
  lld:C0017638 a ncit:C7057 .
  dgn-gda:DGN777c250bdfdb76c2953add6f4fffee7a sio:SIO_000628 miriam-gene:1019 , lld:C0017638 ;
    a sio:SIO_001121 .
}
dgn-np:NP425159.RAlhWKQbSKKwK9S06bTpYV3_RcMPDEwNw3-AN-lNEqCN0130_provenance {
  dgn-np:NP425159.RAlhWKQbSKKwK9S06bTpYV3_RcMPDEwNw3-AN-lNEqCN0130_assertion dcterms:description "[Among the 17 patients in whom the status of the main molecular alterations of gliomas could be evaluated (search for deletions of chromosomes 1p, 19q, 9p, and 10q and amplification of epidermal growth factor receptor, mouse double-minute gene, and cyclin-dependent kinase 4 gene), no relation could be found between the response rate and the type of genetic change (including 1p-19q codeletion).]. 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:19414728 ;
    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:NP425159.RAlhWKQbSKKwK9S06bTpYV3_RcMPDEwNw3-AN-lNEqCN0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:12+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" .
}