@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP907373.RAVKtqjgDxHEfEXJAuAZ7kE2NXSd5f7C6csCKGOX3UCSs> .
@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:NP907373.RAVKtqjgDxHEfEXJAuAZ7kE2NXSd5f7C6csCKGOX3UCSs130_head {
  this: np:hasAssertion dgn-np:NP907373.RAVKtqjgDxHEfEXJAuAZ7kE2NXSd5f7C6csCKGOX3UCSs130_assertion;
    np:hasProvenance dgn-np:NP907373.RAVKtqjgDxHEfEXJAuAZ7kE2NXSd5f7C6csCKGOX3UCSs130_provenance;
    np:hasPublicationInfo dgn-np:NP907373.RAVKtqjgDxHEfEXJAuAZ7kE2NXSd5f7C6csCKGOX3UCSs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP907373.RAVKtqjgDxHEfEXJAuAZ7kE2NXSd5f7C6csCKGOX3UCSs130_assertion a np:Assertion .
  
  dgn-np:NP907373.RAVKtqjgDxHEfEXJAuAZ7kE2NXSd5f7C6csCKGOX3UCSs130_provenance a np:Provenance .
  
  dgn-np:NP907373.RAVKtqjgDxHEfEXJAuAZ7kE2NXSd5f7C6csCKGOX3UCSs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP907373.RAVKtqjgDxHEfEXJAuAZ7kE2NXSd5f7C6csCKGOX3UCSs130_assertion {
  miriam-gene:3481 a ncit:C16612 .
  
  lld:C0023890 a ncit:C7057 .
  
  dgn-gda:DGN9726863debc8aaed9292706d6b76b167 sio:SIO_000628 miriam-gene:3481, lld:C0023890;
    a sio:SIO_001121 .
}

dgn-np:NP907373.RAVKtqjgDxHEfEXJAuAZ7kE2NXSd5f7C6csCKGOX3UCSs130_provenance {
  dgn-np:NP907373.RAVKtqjgDxHEfEXJAuAZ7kE2NXSd5f7C6csCKGOX3UCSs130_assertion dcterms:description
      "[In the present study, changes in the status of genomic imprinting were examined in 15 hepatocellular carcinomas (HCCs) as well as in 29 liver biopsies of chronic hepatitis or liver cirrhosis without clinical evidence of HCC, following screening for heterozygotes with an ApaI polymorphism in IGF2 in 34 HCCs and 80 such non-HCC cases.]. 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:8622877;
    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:NP907373.RAVKtqjgDxHEfEXJAuAZ7kE2NXSd5f7C6csCKGOX3UCSs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:17+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" .
}