@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1016974.RAndA9gOGovMWN183m8oI7pAOc7PQNI6uRaoL2pgmD8tM> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .
dgn-np:NP1016974.RAndA9gOGovMWN183m8oI7pAOc7PQNI6uRaoL2pgmD8tM130_head {
   this: np:hasAssertion dgn-np:NP1016974.RAndA9gOGovMWN183m8oI7pAOc7PQNI6uRaoL2pgmD8tM130_assertion ;
    np:hasProvenance dgn-np:NP1016974.RAndA9gOGovMWN183m8oI7pAOc7PQNI6uRaoL2pgmD8tM130_provenance ;
    np:hasPublicationInfo dgn-np:NP1016974.RAndA9gOGovMWN183m8oI7pAOc7PQNI6uRaoL2pgmD8tM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP1016974.RAndA9gOGovMWN183m8oI7pAOc7PQNI6uRaoL2pgmD8tM130_assertion a np:Assertion .
  dgn-np:NP1016974.RAndA9gOGovMWN183m8oI7pAOc7PQNI6uRaoL2pgmD8tM130_provenance a np:Provenance .
  dgn-np:NP1016974.RAndA9gOGovMWN183m8oI7pAOc7PQNI6uRaoL2pgmD8tM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP1016974.RAndA9gOGovMWN183m8oI7pAOc7PQNI6uRaoL2pgmD8tM130_assertion {
   miriam-gene:100750225 a ncit:C16612 .
  lld:C1527249 a ncit:C7057 .
  dgn-gda:DGN6db1b328e2cc263399ea061642d7d909 sio:SIO_000628 miriam-gene:100750225 , lld:C1527249 ;
    a sio:SIO_001121 .
}
dgn-np:NP1016974.RAndA9gOGovMWN183m8oI7pAOc7PQNI6uRaoL2pgmD8tM130_provenance {
   dgn-np:NP1016974.RAndA9gOGovMWN183m8oI7pAOc7PQNI6uRaoL2pgmD8tM130_assertion dcterms:description "[Combining GISTIC ranking with functional analyses and degree of loss/gain we identify three genes in regions of significant loss (ATP8B1, NARS, and ATP5A1) and eight in regions of gain (CTCFL, SPO11, ZNF217, PLEKHA8, HOXA3, GPNMB, IGF2BP3 and PCAT1) as novel in their association with CRC.]. 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:24204606 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP1016974.RAndA9gOGovMWN183m8oI7pAOc7PQNI6uRaoL2pgmD8tM130_publicationInfo {
   this: dcterms:created "2015-08-25T14:48:11+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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    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> ;
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}