@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP917957.RAtyyV3wpYdmtnRr4MHOZh3PyhNzmAK3mXpbnwD9CSXd4> .
@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/v4.0.0/void/> .
dgn-np:NP917957.RAtyyV3wpYdmtnRr4MHOZh3PyhNzmAK3mXpbnwD9CSXd4130_head {
   this: np:hasAssertion dgn-np:NP917957.RAtyyV3wpYdmtnRr4MHOZh3PyhNzmAK3mXpbnwD9CSXd4130_assertion ;
    np:hasProvenance dgn-np:NP917957.RAtyyV3wpYdmtnRr4MHOZh3PyhNzmAK3mXpbnwD9CSXd4130_provenance ;
    np:hasPublicationInfo dgn-np:NP917957.RAtyyV3wpYdmtnRr4MHOZh3PyhNzmAK3mXpbnwD9CSXd4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP917957.RAtyyV3wpYdmtnRr4MHOZh3PyhNzmAK3mXpbnwD9CSXd4130_assertion a np:Assertion .
  dgn-np:NP917957.RAtyyV3wpYdmtnRr4MHOZh3PyhNzmAK3mXpbnwD9CSXd4130_provenance a np:Provenance .
  dgn-np:NP917957.RAtyyV3wpYdmtnRr4MHOZh3PyhNzmAK3mXpbnwD9CSXd4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP917957.RAtyyV3wpYdmtnRr4MHOZh3PyhNzmAK3mXpbnwD9CSXd4130_assertion {
   miriam-gene:10735 a ncit:C16612 .
  lld:C0017636 a ncit:C7057 .
  dgn-gda:DGN855b6a3ff1fb58dbbdc15be2f084de93 sio:SIO_000628 miriam-gene:10735 , lld:C0017636 ;
    a sio:SIO_001121 .
}
dgn-np:NP917957.RAtyyV3wpYdmtnRr4MHOZh3PyhNzmAK3mXpbnwD9CSXd4130_provenance {
   dgn-np:NP917957.RAtyyV3wpYdmtnRr4MHOZh3PyhNzmAK3mXpbnwD9CSXd4130_assertion dcterms:description "[Studying a near-diploid human cell line with a stable karyotype, we found that targeted inactivation of STAG2 led to chromatid cohesion defects and aneuploidy, whereas in two aneuploid human glioblastoma cell lines, targeted correction of the endogenous mutant alleles of STAG2 led to enhanced chromosomal stability.]. 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:21852505 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP917957.RAtyyV3wpYdmtnRr4MHOZh3PyhNzmAK3mXpbnwD9CSXd4130_publicationInfo {
   this: dcterms:created "2016-05-13T12:48:40+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:disgenetv3.0rdf ;
    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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}