@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP935429.RA_G6gsgtHP0a0MAG4lx31vd8EExRofxIdxbB5Vp0WilI> .
@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:NP935429.RA_G6gsgtHP0a0MAG4lx31vd8EExRofxIdxbB5Vp0WilI130_head {
  this: np:hasAssertion dgn-np:NP935429.RA_G6gsgtHP0a0MAG4lx31vd8EExRofxIdxbB5Vp0WilI130_assertion;
    np:hasProvenance dgn-np:NP935429.RA_G6gsgtHP0a0MAG4lx31vd8EExRofxIdxbB5Vp0WilI130_provenance;
    np:hasPublicationInfo dgn-np:NP935429.RA_G6gsgtHP0a0MAG4lx31vd8EExRofxIdxbB5Vp0WilI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP935429.RA_G6gsgtHP0a0MAG4lx31vd8EExRofxIdxbB5Vp0WilI130_assertion a np:Assertion .
  
  dgn-np:NP935429.RA_G6gsgtHP0a0MAG4lx31vd8EExRofxIdxbB5Vp0WilI130_provenance a np:Provenance .
  
  dgn-np:NP935429.RA_G6gsgtHP0a0MAG4lx31vd8EExRofxIdxbB5Vp0WilI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP935429.RA_G6gsgtHP0a0MAG4lx31vd8EExRofxIdxbB5Vp0WilI130_assertion {
  miriam-gene:5728 a ncit:C16612 .
  
  lld:C0019196 a ncit:C7057 .
  
  dgn-gda:DGNecdea3e9602d1c0009655f5c430131d5 sio:SIO_000628 miriam-gene:5728, lld:C0019196;
    a sio:SIO_001121 .
}

dgn-np:NP935429.RA_G6gsgtHP0a0MAG4lx31vd8EExRofxIdxbB5Vp0WilI130_provenance {
  dgn-np:NP935429.RA_G6gsgtHP0a0MAG4lx31vd8EExRofxIdxbB5Vp0WilI130_assertion dcterms:description
      "[Accumulating evidence indicates that alterations of PTEN expression and activity in hepatocytes are common and recurrent molecular events associated with liver disorders of various etiologies including obesity, the metabolic syndrome, hepatitis B virus/hepatitis C virus infection and abusive alcohol consumption.]. 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:20460918;
    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:NP935429.RA_G6gsgtHP0a0MAG4lx31vd8EExRofxIdxbB5Vp0WilI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:33+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" .
}