@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP682532.RASRILiXEiCQPhqDpMd3rwWaPAV7c6BvC1Cqwca1XdkaU> .
@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:NP682532.RASRILiXEiCQPhqDpMd3rwWaPAV7c6BvC1Cqwca1XdkaU130_head {
  this: np:hasAssertion dgn-np:NP682532.RASRILiXEiCQPhqDpMd3rwWaPAV7c6BvC1Cqwca1XdkaU130_assertion;
    np:hasProvenance dgn-np:NP682532.RASRILiXEiCQPhqDpMd3rwWaPAV7c6BvC1Cqwca1XdkaU130_provenance;
    np:hasPublicationInfo dgn-np:NP682532.RASRILiXEiCQPhqDpMd3rwWaPAV7c6BvC1Cqwca1XdkaU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP682532.RASRILiXEiCQPhqDpMd3rwWaPAV7c6BvC1Cqwca1XdkaU130_assertion a np:Assertion .
  
  dgn-np:NP682532.RASRILiXEiCQPhqDpMd3rwWaPAV7c6BvC1Cqwca1XdkaU130_provenance a np:Provenance .
  
  dgn-np:NP682532.RASRILiXEiCQPhqDpMd3rwWaPAV7c6BvC1Cqwca1XdkaU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP682532.RASRILiXEiCQPhqDpMd3rwWaPAV7c6BvC1Cqwca1XdkaU130_assertion {
  miriam-gene:283120 a ncit:C16612 .
  
  lld:C0022739 a ncit:C7057 .
  
  dgn-gda:DGN9e6b4807fb027f61e2dceb6b17bd6fa6 sio:SIO_000628 miriam-gene:283120, lld:C0022739;
    a sio:SIO_001121 .
}

dgn-np:NP682532.RASRILiXEiCQPhqDpMd3rwWaPAV7c6BvC1Cqwca1XdkaU130_provenance {
  dgn-np:NP682532.RASRILiXEiCQPhqDpMd3rwWaPAV7c6BvC1Cqwca1XdkaU130_assertion dcterms:description
      "[Analysis of these data also indicates that loss of IGF2 imprinting is not necessarily linked to alteration of methylation at the KvDMR1 or H19 loci and supports the notion that IGF2 overexpression is involved in the etiology of the tissue hypertrophy observed in different overgrowth disorders, including KTWS.]. 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:10712200;
    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:NP682532.RASRILiXEiCQPhqDpMd3rwWaPAV7c6BvC1Cqwca1XdkaU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:55+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" .
}