@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP424620.RAwOEHAbcKrVPx5ubVfs4OgQTuUKetbdxp89hrEyynZ0E> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP424620.RAwOEHAbcKrVPx5ubVfs4OgQTuUKetbdxp89hrEyynZ0E130_head {
  this: np:hasAssertion dgn-np:NP424620.RAwOEHAbcKrVPx5ubVfs4OgQTuUKetbdxp89hrEyynZ0E130_assertion;
    np:hasProvenance dgn-np:NP424620.RAwOEHAbcKrVPx5ubVfs4OgQTuUKetbdxp89hrEyynZ0E130_provenance;
    np:hasPublicationInfo dgn-np:NP424620.RAwOEHAbcKrVPx5ubVfs4OgQTuUKetbdxp89hrEyynZ0E130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP424620.RAwOEHAbcKrVPx5ubVfs4OgQTuUKetbdxp89hrEyynZ0E130_assertion a np:Assertion .
  
  dgn-np:NP424620.RAwOEHAbcKrVPx5ubVfs4OgQTuUKetbdxp89hrEyynZ0E130_provenance a np:Provenance .
  
  dgn-np:NP424620.RAwOEHAbcKrVPx5ubVfs4OgQTuUKetbdxp89hrEyynZ0E130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP424620.RAwOEHAbcKrVPx5ubVfs4OgQTuUKetbdxp89hrEyynZ0E130_assertion {
  miriam-gene:3621 a ncit:C16612 .
  
  lld:C0017638 a ncit:C7057 .
  
  dgn-gda:DGN67370830a0235372c0260912a812b645 sio:SIO_000628 miriam-gene:3621, lld:C0017638;
    a sio:SIO_001121 .
}

dgn-np:NP424620.RAwOEHAbcKrVPx5ubVfs4OgQTuUKetbdxp89hrEyynZ0E130_provenance {
  dgn-np:NP424620.RAwOEHAbcKrVPx5ubVfs4OgQTuUKetbdxp89hrEyynZ0E130_assertion dcterms:description
      "[Our data indicate that although mutations of ING1 seem to be infrequent in human brain tumors, deregulated expression and mislocalization of ING1 proteins, particularly the p33ING1b isoform, are common events in gliomas and 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:14676120;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP424620.RAwOEHAbcKrVPx5ubVfs4OgQTuUKetbdxp89hrEyynZ0E130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:57+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}