@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1330900.RA46NDXQVlaJ7qn7MbhXIu4UkTQp5W30e2A5MAzioMXHA> .
@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:NP1330900.RA46NDXQVlaJ7qn7MbhXIu4UkTQp5W30e2A5MAzioMXHA130_head {
  this: np:hasAssertion dgn-np:NP1330900.RA46NDXQVlaJ7qn7MbhXIu4UkTQp5W30e2A5MAzioMXHA130_assertion;
    np:hasProvenance dgn-np:NP1330900.RA46NDXQVlaJ7qn7MbhXIu4UkTQp5W30e2A5MAzioMXHA130_provenance;
    np:hasPublicationInfo dgn-np:NP1330900.RA46NDXQVlaJ7qn7MbhXIu4UkTQp5W30e2A5MAzioMXHA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1330900.RA46NDXQVlaJ7qn7MbhXIu4UkTQp5W30e2A5MAzioMXHA130_assertion a np:Assertion .
  
  dgn-np:NP1330900.RA46NDXQVlaJ7qn7MbhXIu4UkTQp5W30e2A5MAzioMXHA130_provenance a np:Provenance .
  
  dgn-np:NP1330900.RA46NDXQVlaJ7qn7MbhXIu4UkTQp5W30e2A5MAzioMXHA130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1330900.RA46NDXQVlaJ7qn7MbhXIu4UkTQp5W30e2A5MAzioMXHA130_assertion {
  miriam-gene:3481 a ncit:C16612 .
  
  lld:C0004903 a ncit:C7057 .
  
  dgn-gda:DGN532d2cb23cd586d8c2ace56df607e241 sio:SIO_000628 miriam-gene:3481, lld:C0004903;
    a sio:SIO_001121 .
}

dgn-np:NP1330900.RA46NDXQVlaJ7qn7MbhXIu4UkTQp5W30e2A5MAzioMXHA130_provenance {
  dgn-np:NP1330900.RA46NDXQVlaJ7qn7MbhXIu4UkTQp5W30e2A5MAzioMXHA130_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-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:NP1330900.RA46NDXQVlaJ7qn7MbhXIu4UkTQp5W30e2A5MAzioMXHA130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:49+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" .
}