@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP484170.RAUkTGXQi5L3tz74RLtAsRMf5hw2iF7ucSrvg3CQXA3dU> .
@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/v3.0.0/void/> .

dgn-np:NP484170.RAUkTGXQi5L3tz74RLtAsRMf5hw2iF7ucSrvg3CQXA3dU130_head {
  this: np:hasAssertion dgn-np:NP484170.RAUkTGXQi5L3tz74RLtAsRMf5hw2iF7ucSrvg3CQXA3dU130_assertion;
    np:hasProvenance dgn-np:NP484170.RAUkTGXQi5L3tz74RLtAsRMf5hw2iF7ucSrvg3CQXA3dU130_provenance;
    np:hasPublicationInfo dgn-np:NP484170.RAUkTGXQi5L3tz74RLtAsRMf5hw2iF7ucSrvg3CQXA3dU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP484170.RAUkTGXQi5L3tz74RLtAsRMf5hw2iF7ucSrvg3CQXA3dU130_assertion a np:Assertion .
  
  dgn-np:NP484170.RAUkTGXQi5L3tz74RLtAsRMf5hw2iF7ucSrvg3CQXA3dU130_provenance a np:Provenance .
  
  dgn-np:NP484170.RAUkTGXQi5L3tz74RLtAsRMf5hw2iF7ucSrvg3CQXA3dU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP484170.RAUkTGXQi5L3tz74RLtAsRMf5hw2iF7ucSrvg3CQXA3dU130_assertion {
  miriam-gene:3481 a ncit:C16612 .
  
  lld:C1882062 a ncit:C7057 .
  
  dgn-gda:DGNb6455e8a9ab67775a100368ff2f55079 sio:SIO_000628 miriam-gene:3481, lld:C1882062;
    a sio:SIO_001121 .
}

dgn-np:NP484170.RAUkTGXQi5L3tz74RLtAsRMf5hw2iF7ucSrvg3CQXA3dU130_provenance {
  dgn-np:NP484170.RAUkTGXQi5L3tz74RLtAsRMf5hw2iF7ucSrvg3CQXA3dU130_assertion dcterms:description
      "[Here, we review a recent study showing that a mouse model of loss of imprinting (LOI) of the insulin-like growth factor II gene (Igf2), which shows aberrant activation of the normally silent maternal allele, modifies the risk of intestinal neoplasia caused by mutations of the adenomatous polyposis coli (Apc) gene.]. 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:16357124;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP484170.RAUkTGXQi5L3tz74RLtAsRMf5hw2iF7ucSrvg3CQXA3dU130_publicationInfo {
  this: dcterms:created "2015-08-25T14:42:25+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}