@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP658887.RAfg_d2ypHNlCwQlPULq7jVCaHfPbDTzlhgEAgOy40ci4> .
@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:NP658887.RAfg_d2ypHNlCwQlPULq7jVCaHfPbDTzlhgEAgOy40ci4130_head {
  this: np:hasAssertion dgn-np:NP658887.RAfg_d2ypHNlCwQlPULq7jVCaHfPbDTzlhgEAgOy40ci4130_assertion ;
    np:hasProvenance dgn-np:NP658887.RAfg_d2ypHNlCwQlPULq7jVCaHfPbDTzlhgEAgOy40ci4130_provenance ;
    np:hasPublicationInfo dgn-np:NP658887.RAfg_d2ypHNlCwQlPULq7jVCaHfPbDTzlhgEAgOy40ci4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP658887.RAfg_d2ypHNlCwQlPULq7jVCaHfPbDTzlhgEAgOy40ci4130_assertion a np:Assertion .
  dgn-np:NP658887.RAfg_d2ypHNlCwQlPULq7jVCaHfPbDTzlhgEAgOy40ci4130_provenance a np:Provenance .
  dgn-np:NP658887.RAfg_d2ypHNlCwQlPULq7jVCaHfPbDTzlhgEAgOy40ci4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP658887.RAfg_d2ypHNlCwQlPULq7jVCaHfPbDTzlhgEAgOy40ci4130_assertion {
  miriam-gene:324 a ncit:C16612 .
  lld:C2239176 a ncit:C7057 .
  dgn-gda:DGN696f1f78269f79dad42174554c3a7ccc sio:SIO_000628 miriam-gene:324 , lld:C2239176 ;
    a sio:SIO_001121 .
}
dgn-np:NP658887.RAfg_d2ypHNlCwQlPULq7jVCaHfPbDTzlhgEAgOy40ci4130_provenance {
  dgn-np:NP658887.RAfg_d2ypHNlCwQlPULq7jVCaHfPbDTzlhgEAgOy40ci4130_assertion dcterms:description "[The low frequency of CTNNB1 mutations, however, suggests that mutation of another Wnt signaling component, such as the Wnt scaffolding protein axin or the adenomatous polyposis coli protein, both of which modulate beta-catenin stability, also may be involved in aflatoxin-associated HCC.]. 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:11429783 ;
    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:NP658887.RAfg_d2ypHNlCwQlPULq7jVCaHfPbDTzlhgEAgOy40ci4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:38+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" .
}