@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP876823.RAB-CY56_9wB93fAkCs8SaFHQrfbDYwLLsqaDBiaWCeuI> .
@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:NP876823.RAB-CY56_9wB93fAkCs8SaFHQrfbDYwLLsqaDBiaWCeuI130_head {
  this: np:hasAssertion dgn-np:NP876823.RAB-CY56_9wB93fAkCs8SaFHQrfbDYwLLsqaDBiaWCeuI130_assertion;
    np:hasProvenance dgn-np:NP876823.RAB-CY56_9wB93fAkCs8SaFHQrfbDYwLLsqaDBiaWCeuI130_provenance;
    np:hasPublicationInfo dgn-np:NP876823.RAB-CY56_9wB93fAkCs8SaFHQrfbDYwLLsqaDBiaWCeuI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP876823.RAB-CY56_9wB93fAkCs8SaFHQrfbDYwLLsqaDBiaWCeuI130_assertion a np:Assertion .
  
  dgn-np:NP876823.RAB-CY56_9wB93fAkCs8SaFHQrfbDYwLLsqaDBiaWCeuI130_provenance a np:Provenance .
  
  dgn-np:NP876823.RAB-CY56_9wB93fAkCs8SaFHQrfbDYwLLsqaDBiaWCeuI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP876823.RAB-CY56_9wB93fAkCs8SaFHQrfbDYwLLsqaDBiaWCeuI130_assertion {
  miriam-gene:3481 a ncit:C16612 .
  
  lld:C0041107 a ncit:C7057 .
  
  dgn-gda:DGNd395a36e5118d516f7d243c4c8138599 sio:SIO_000628 miriam-gene:3481, lld:C0041107;
    a sio:SIO_001121 .
}

dgn-np:NP876823.RAB-CY56_9wB93fAkCs8SaFHQrfbDYwLLsqaDBiaWCeuI130_provenance {
  dgn-np:NP876823.RAB-CY56_9wB93fAkCs8SaFHQrfbDYwLLsqaDBiaWCeuI130_assertion dcterms:description
      "[In contrast to previous reports in which imprinting of the growth stimulator gene, IGF2, has been invoked as the mechanism explaining sporadic cases of BWS (especially in situations where uniparental disomy and trisomy of the 11p15.5 region has occurred), it is suggested that paternal imprinting of a growth suppressor gene, e.g., H19, may be one of the causes of familial BWS.]. 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:8055321;
    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:NP876823.RAB-CY56_9wB93fAkCs8SaFHQrfbDYwLLsqaDBiaWCeuI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:56+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" .
}