@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP614227.RAKTy48AoLeD6RhtTqSisYmRBsHGGr9SOgpG5RseRQ2io> .
@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:NP614227.RAKTy48AoLeD6RhtTqSisYmRBsHGGr9SOgpG5RseRQ2io130_head {
  this: np:hasAssertion dgn-np:NP614227.RAKTy48AoLeD6RhtTqSisYmRBsHGGr9SOgpG5RseRQ2io130_assertion ;
    np:hasProvenance dgn-np:NP614227.RAKTy48AoLeD6RhtTqSisYmRBsHGGr9SOgpG5RseRQ2io130_provenance ;
    np:hasPublicationInfo dgn-np:NP614227.RAKTy48AoLeD6RhtTqSisYmRBsHGGr9SOgpG5RseRQ2io130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP614227.RAKTy48AoLeD6RhtTqSisYmRBsHGGr9SOgpG5RseRQ2io130_assertion a np:Assertion .
  dgn-np:NP614227.RAKTy48AoLeD6RhtTqSisYmRBsHGGr9SOgpG5RseRQ2io130_provenance a np:Provenance .
  dgn-np:NP614227.RAKTy48AoLeD6RhtTqSisYmRBsHGGr9SOgpG5RseRQ2io130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP614227.RAKTy48AoLeD6RhtTqSisYmRBsHGGr9SOgpG5RseRQ2io130_assertion {
  miriam-gene:4609 a ncit:C16612 .
  lld:C0677898 a ncit:C7057 .
  dgn-gda:DGN9712f893b43980546f024689d70546b8 sio:SIO_000628 miriam-gene:4609 , lld:C0677898 ;
    a sio:SIO_001121 .
}
dgn-np:NP614227.RAKTy48AoLeD6RhtTqSisYmRBsHGGr9SOgpG5RseRQ2io130_provenance {
  dgn-np:NP614227.RAKTy48AoLeD6RhtTqSisYmRBsHGGr9SOgpG5RseRQ2io130_assertion dcterms:description "[Quantitative Real Time RT-PCR was performed on 45 foci representing the histological spectrum from normal to invasive cancer, using specific primer sets for alternative splice variants that differ by the presence (16A) or absence (16B) of a 159-bp noncoding segment of exon 16 of CTNNB1, in conjunction with downstream targets MYC and WAF1.]. 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:16114033 ;
    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:NP614227.RAKTy48AoLeD6RhtTqSisYmRBsHGGr9SOgpG5RseRQ2io130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:11+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" .
}