@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP514392.RAN5ybMJL3Gvbi-v_slxeb9W4gUrjZLQ1EEqIsMSNXGEc> .
@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:NP514392.RAN5ybMJL3Gvbi-v_slxeb9W4gUrjZLQ1EEqIsMSNXGEc130_head {
   this: np:hasAssertion dgn-np:NP514392.RAN5ybMJL3Gvbi-v_slxeb9W4gUrjZLQ1EEqIsMSNXGEc130_assertion ;
    np:hasProvenance dgn-np:NP514392.RAN5ybMJL3Gvbi-v_slxeb9W4gUrjZLQ1EEqIsMSNXGEc130_provenance ;
    np:hasPublicationInfo dgn-np:NP514392.RAN5ybMJL3Gvbi-v_slxeb9W4gUrjZLQ1EEqIsMSNXGEc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP514392.RAN5ybMJL3Gvbi-v_slxeb9W4gUrjZLQ1EEqIsMSNXGEc130_assertion a np:Assertion .
  dgn-np:NP514392.RAN5ybMJL3Gvbi-v_slxeb9W4gUrjZLQ1EEqIsMSNXGEc130_provenance a np:Provenance .
  dgn-np:NP514392.RAN5ybMJL3Gvbi-v_slxeb9W4gUrjZLQ1EEqIsMSNXGEc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP514392.RAN5ybMJL3Gvbi-v_slxeb9W4gUrjZLQ1EEqIsMSNXGEc130_assertion {
   miriam-gene:23152 a ncit:C16612 .
  lld:C0017638 a ncit:C7057 .
  dgn-gda:DGNf6a9c2b0fcee104a6fa559c015d26450 sio:SIO_000628 miriam-gene:23152 , lld:C0017638 ;
    a sio:SIO_001121 .
}
dgn-np:NP514392.RAN5ybMJL3Gvbi-v_slxeb9W4gUrjZLQ1EEqIsMSNXGEc130_provenance {
   dgn-np:NP514392.RAN5ybMJL3Gvbi-v_slxeb9W4gUrjZLQ1EEqIsMSNXGEc130_assertion dcterms:description "[Moreover, large-scale molecular profiling approaches have identified new mutations in gliomas, affecting IDH1, IDH2, H3F3, ATRX, and CIC, which has allowed subclassification of gliomas into distinct molecular subgroups with characteristic features of age, localisation, and outcome.]. 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:23896276 ;
    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:NP514392.RAN5ybMJL3Gvbi-v_slxeb9W4gUrjZLQ1EEqIsMSNXGEc130_publicationInfo {
   this: dcterms:created "2014-10-02T12:37:06+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" .
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}