@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP768885.RArTj6yW4TqFRGHUN1GcakTp4TZKkX9ZqGe8M_ZtreJJ8> .
@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:NP768885.RArTj6yW4TqFRGHUN1GcakTp4TZKkX9ZqGe8M_ZtreJJ8130_head {
  this: np:hasAssertion dgn-np:NP768885.RArTj6yW4TqFRGHUN1GcakTp4TZKkX9ZqGe8M_ZtreJJ8130_assertion ;
    np:hasProvenance dgn-np:NP768885.RArTj6yW4TqFRGHUN1GcakTp4TZKkX9ZqGe8M_ZtreJJ8130_provenance ;
    np:hasPublicationInfo dgn-np:NP768885.RArTj6yW4TqFRGHUN1GcakTp4TZKkX9ZqGe8M_ZtreJJ8130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP768885.RArTj6yW4TqFRGHUN1GcakTp4TZKkX9ZqGe8M_ZtreJJ8130_assertion a np:Assertion .
  dgn-np:NP768885.RArTj6yW4TqFRGHUN1GcakTp4TZKkX9ZqGe8M_ZtreJJ8130_provenance a np:Provenance .
  dgn-np:NP768885.RArTj6yW4TqFRGHUN1GcakTp4TZKkX9ZqGe8M_ZtreJJ8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP768885.RArTj6yW4TqFRGHUN1GcakTp4TZKkX9ZqGe8M_ZtreJJ8130_assertion {
  miriam-gene:2735 a ncit:C16612 .
  lld:C0025149 a ncit:C7057 .
  dgn-gda:DGN23cde791688819b033791fc9b1b8fb91 sio:SIO_000628 miriam-gene:2735 , lld:C0025149 ;
    a sio:SIO_001121 .
}
dgn-np:NP768885.RArTj6yW4TqFRGHUN1GcakTp4TZKkX9ZqGe8M_ZtreJJ8130_provenance {
  dgn-np:NP768885.RArTj6yW4TqFRGHUN1GcakTp4TZKkX9ZqGe8M_ZtreJJ8130_assertion dcterms:description "[The GLI1 mRNA is highly edited at nucleotide 2179 by adenosine deamination in normal cerebellum, but the extent of this modification is reduced in cell lines from the cerebellar tumor medulloblastoma.]. 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:23324600 ;
    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:NP768885.RArTj6yW4TqFRGHUN1GcakTp4TZKkX9ZqGe8M_ZtreJJ8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:45+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" .
}