@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP620330.RAeQLOTdr4E1xx6l-jotRPcLxO0aZKUEVY7FVX4vFRGow> .
@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:NP620330.RAeQLOTdr4E1xx6l-jotRPcLxO0aZKUEVY7FVX4vFRGow130_head {
  this: np:hasAssertion dgn-np:NP620330.RAeQLOTdr4E1xx6l-jotRPcLxO0aZKUEVY7FVX4vFRGow130_assertion;
    np:hasProvenance dgn-np:NP620330.RAeQLOTdr4E1xx6l-jotRPcLxO0aZKUEVY7FVX4vFRGow130_provenance;
    np:hasPublicationInfo dgn-np:NP620330.RAeQLOTdr4E1xx6l-jotRPcLxO0aZKUEVY7FVX4vFRGow130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP620330.RAeQLOTdr4E1xx6l-jotRPcLxO0aZKUEVY7FVX4vFRGow130_assertion a np:Assertion .
  
  dgn-np:NP620330.RAeQLOTdr4E1xx6l-jotRPcLxO0aZKUEVY7FVX4vFRGow130_provenance a np:Provenance .
  
  dgn-np:NP620330.RAeQLOTdr4E1xx6l-jotRPcLxO0aZKUEVY7FVX4vFRGow130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP620330.RAeQLOTdr4E1xx6l-jotRPcLxO0aZKUEVY7FVX4vFRGow130_assertion {
  miriam-gene:3621 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGN553bc56a41fea634e72fc3d45447fc74 sio:SIO_000628 miriam-gene:3621, lld:C0006826;
    a sio:SIO_001121 .
}

dgn-np:NP620330.RAeQLOTdr4E1xx6l-jotRPcLxO0aZKUEVY7FVX4vFRGow130_provenance {
  dgn-np:NP620330.RAeQLOTdr4E1xx6l-jotRPcLxO0aZKUEVY7FVX4vFRGow130_assertion dcterms:description
      "[Furthermore, N216S, V218I, and G221V mutations, found in human malignancies, impair the ability of ING1 to associate with H3K4me3 or to induce nucleotide repair and cell death, linking the tumorigenic activity of ING1 with epigenetic regulation.]. 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:18533182;
    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:NP620330.RAeQLOTdr4E1xx6l-jotRPcLxO0aZKUEVY7FVX4vFRGow130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:14+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" .
}