@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP588089.RAt5BYqhNSNR2A8G8jBZ2R0fwpPBMf9ifxQIXUBJSmEMs> .
@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:NP588089.RAt5BYqhNSNR2A8G8jBZ2R0fwpPBMf9ifxQIXUBJSmEMs130_head {
  this: np:hasAssertion dgn-np:NP588089.RAt5BYqhNSNR2A8G8jBZ2R0fwpPBMf9ifxQIXUBJSmEMs130_assertion ;
    np:hasProvenance dgn-np:NP588089.RAt5BYqhNSNR2A8G8jBZ2R0fwpPBMf9ifxQIXUBJSmEMs130_provenance ;
    np:hasPublicationInfo dgn-np:NP588089.RAt5BYqhNSNR2A8G8jBZ2R0fwpPBMf9ifxQIXUBJSmEMs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP588089.RAt5BYqhNSNR2A8G8jBZ2R0fwpPBMf9ifxQIXUBJSmEMs130_assertion a np:Assertion .
  dgn-np:NP588089.RAt5BYqhNSNR2A8G8jBZ2R0fwpPBMf9ifxQIXUBJSmEMs130_provenance a np:Provenance .
  dgn-np:NP588089.RAt5BYqhNSNR2A8G8jBZ2R0fwpPBMf9ifxQIXUBJSmEMs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP588089.RAt5BYqhNSNR2A8G8jBZ2R0fwpPBMf9ifxQIXUBJSmEMs130_assertion {
  miriam-gene:7764 a ncit:C16612 .
  lld:C0009402 a ncit:C7057 .
  dgn-gda:DGN131fb31c1c2e976997020fdc7372ad56 sio:SIO_000628 miriam-gene:7764 , lld:C0009402 ;
    a sio:SIO_001121 .
}
dgn-np:NP588089.RAt5BYqhNSNR2A8G8jBZ2R0fwpPBMf9ifxQIXUBJSmEMs130_provenance {
  dgn-np:NP588089.RAt5BYqhNSNR2A8G8jBZ2R0fwpPBMf9ifxQIXUBJSmEMs130_assertion dcterms:description "[We investigated the copy number of the 20q13.2 region including the ZNF217 oncogene in 17 nonmetastatic colorectal cancers (CRCs), 18 primary CRC tumors with liver metastasis, and 18 metastatic lesions by two-color fluorescence in situ hybridization to evaluate the significance of an increased copy number of 20q13.2 in CRC, especially in those cases with liver metastasis.]. 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:10914715 ;
    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:NP588089.RAt5BYqhNSNR2A8G8jBZ2R0fwpPBMf9ifxQIXUBJSmEMs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:54+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" .
}