@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP201602.RAhGRfI_koGmGFDppui-Q0ojW19AtgJHTGpzBCc-0bOBw> .
@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:NP201602.RAhGRfI_koGmGFDppui-Q0ojW19AtgJHTGpzBCc-0bOBw130_head {
  this: np:hasAssertion dgn-np:NP201602.RAhGRfI_koGmGFDppui-Q0ojW19AtgJHTGpzBCc-0bOBw130_assertion;
    np:hasProvenance dgn-np:NP201602.RAhGRfI_koGmGFDppui-Q0ojW19AtgJHTGpzBCc-0bOBw130_provenance;
    np:hasPublicationInfo dgn-np:NP201602.RAhGRfI_koGmGFDppui-Q0ojW19AtgJHTGpzBCc-0bOBw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP201602.RAhGRfI_koGmGFDppui-Q0ojW19AtgJHTGpzBCc-0bOBw130_assertion a np:Assertion .
  
  dgn-np:NP201602.RAhGRfI_koGmGFDppui-Q0ojW19AtgJHTGpzBCc-0bOBw130_provenance a np:Provenance .
  
  dgn-np:NP201602.RAhGRfI_koGmGFDppui-Q0ojW19AtgJHTGpzBCc-0bOBw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP201602.RAhGRfI_koGmGFDppui-Q0ojW19AtgJHTGpzBCc-0bOBw130_assertion {
  miriam-gene:3481 a ncit:C16612 .
  
  lld:C0004903 a ncit:C7057 .
  
  dgn-gda:DGNacfd40179f4b172e1fc10a915ec46b09 sio:SIO_000628 miriam-gene:3481, lld:C0004903;
    a sio:SIO_001121 .
}

dgn-np:NP201602.RAhGRfI_koGmGFDppui-Q0ojW19AtgJHTGpzBCc-0bOBw130_provenance {
  dgn-np:NP201602.RAhGRfI_koGmGFDppui-Q0ojW19AtgJHTGpzBCc-0bOBw130_assertion dcterms:description
      "[These results suggest that (1) loss of imprinting (LOI) of IGF2 might be responsible for BWS, (2) on the other hand, LOI itself might not induce tumor occurrence in tissues where the control of tissue-specific expression of IGF2 is maintained, (3) increased expression of IGF2 due to maternal loss of a putative controller gene for IGF2 at 11p15 might predispose to sustaining tumorigenic mutations and tumor progression, (4) loss of a putative onco-suppressor gene at 11p15 might induce RMS occurrence.]. 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:8086640;
    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:NP201602.RAhGRfI_koGmGFDppui-Q0ojW19AtgJHTGpzBCc-0bOBw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:51+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" .
}