@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP536881.RAsniGNW-0JRsls3fj1MDWSheOpRysrVTPlBompKh8uwA> .
@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:NP536881.RAsniGNW-0JRsls3fj1MDWSheOpRysrVTPlBompKh8uwA130_head {
  this: np:hasAssertion dgn-np:NP536881.RAsniGNW-0JRsls3fj1MDWSheOpRysrVTPlBompKh8uwA130_assertion;
    np:hasProvenance dgn-np:NP536881.RAsniGNW-0JRsls3fj1MDWSheOpRysrVTPlBompKh8uwA130_provenance;
    np:hasPublicationInfo dgn-np:NP536881.RAsniGNW-0JRsls3fj1MDWSheOpRysrVTPlBompKh8uwA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP536881.RAsniGNW-0JRsls3fj1MDWSheOpRysrVTPlBompKh8uwA130_assertion a np:Assertion .
  
  dgn-np:NP536881.RAsniGNW-0JRsls3fj1MDWSheOpRysrVTPlBompKh8uwA130_provenance a np:Provenance .
  
  dgn-np:NP536881.RAsniGNW-0JRsls3fj1MDWSheOpRysrVTPlBompKh8uwA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP536881.RAsniGNW-0JRsls3fj1MDWSheOpRysrVTPlBompKh8uwA130_assertion {
  miriam-gene:728458 a ncit:C16612 .
  
  lld:C0220603 a ncit:C7057 .
  
  dgn-gda:DGNe5586c29dd19da909d5d4f9d9559be27 sio:SIO_000628 miriam-gene:728458, lld:C0220603;
    a sio:SIO_001121 .
}

dgn-np:NP536881.RAsniGNW-0JRsls3fj1MDWSheOpRysrVTPlBompKh8uwA130_provenance {
  dgn-np:NP536881.RAsniGNW-0JRsls3fj1MDWSheOpRysrVTPlBompKh8uwA130_assertion dcterms:description
      "[Medulloblastoma (MB) is the most common malignant pediatric brain tumor and is thought to arise from genetic anomalies in developmental pathways required for the normal maturation of the cerebellar cortex, notably developmental pathways for granule cell progenitor (GCP) neurogenesis.]. 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:21315459;
    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:NP536881.RAsniGNW-0JRsls3fj1MDWSheOpRysrVTPlBompKh8uwA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:24+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" .
}