@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP425140.RACWBHGLOcqQ1Cb777Bo5MjdjrgiSiv85rIjTc9csBkAw> .
@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:NP425140.RACWBHGLOcqQ1Cb777Bo5MjdjrgiSiv85rIjTc9csBkAw130_head {
  this: np:hasAssertion dgn-np:NP425140.RACWBHGLOcqQ1Cb777Bo5MjdjrgiSiv85rIjTc9csBkAw130_assertion;
    np:hasProvenance dgn-np:NP425140.RACWBHGLOcqQ1Cb777Bo5MjdjrgiSiv85rIjTc9csBkAw130_provenance;
    np:hasPublicationInfo dgn-np:NP425140.RACWBHGLOcqQ1Cb777Bo5MjdjrgiSiv85rIjTc9csBkAw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP425140.RACWBHGLOcqQ1Cb777Bo5MjdjrgiSiv85rIjTc9csBkAw130_assertion a np:Assertion .
  
  dgn-np:NP425140.RACWBHGLOcqQ1Cb777Bo5MjdjrgiSiv85rIjTc9csBkAw130_provenance a np:Provenance .
  
  dgn-np:NP425140.RACWBHGLOcqQ1Cb777Bo5MjdjrgiSiv85rIjTc9csBkAw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP425140.RACWBHGLOcqQ1Cb777Bo5MjdjrgiSiv85rIjTc9csBkAw130_assertion {
  miriam-gene:6927 a ncit:C16612 .
  
  lld:C0541760 a ncit:C7057 .
  
  dgn-gda:DGN25a10b10b43643f9c93af9adbedc9186 sio:SIO_000628 miriam-gene:6927, lld:C0541760;
    a sio:SIO_001121 .
}

dgn-np:NP425140.RACWBHGLOcqQ1Cb777Bo5MjdjrgiSiv85rIjTc9csBkAw130_provenance {
  dgn-np:NP425140.RACWBHGLOcqQ1Cb777Bo5MjdjrgiSiv85rIjTc9csBkAw130_assertion dcterms:description
      "[These results indicate that inactivation of TCF1, whether sporadic or associated with MODY3, is an important genetic event in the occurrence of human liver adenoma, and may be an early step in the development of some HCCs.]. 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:12355088;
    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:NP425140.RACWBHGLOcqQ1Cb777Bo5MjdjrgiSiv85rIjTc9csBkAw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:12+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" .
}