@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP758639.RAn7Q2FHTJPalsb-Je_paSbH5kQ1LJE5zv2w0z5MNuQ34> .
@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:NP758639.RAn7Q2FHTJPalsb-Je_paSbH5kQ1LJE5zv2w0z5MNuQ34130_head {
  this: np:hasAssertion dgn-np:NP758639.RAn7Q2FHTJPalsb-Je_paSbH5kQ1LJE5zv2w0z5MNuQ34130_assertion ;
    np:hasProvenance dgn-np:NP758639.RAn7Q2FHTJPalsb-Je_paSbH5kQ1LJE5zv2w0z5MNuQ34130_provenance ;
    np:hasPublicationInfo dgn-np:NP758639.RAn7Q2FHTJPalsb-Je_paSbH5kQ1LJE5zv2w0z5MNuQ34130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP758639.RAn7Q2FHTJPalsb-Je_paSbH5kQ1LJE5zv2w0z5MNuQ34130_assertion a np:Assertion .
  dgn-np:NP758639.RAn7Q2FHTJPalsb-Je_paSbH5kQ1LJE5zv2w0z5MNuQ34130_provenance a np:Provenance .
  dgn-np:NP758639.RAn7Q2FHTJPalsb-Je_paSbH5kQ1LJE5zv2w0z5MNuQ34130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP758639.RAn7Q2FHTJPalsb-Je_paSbH5kQ1LJE5zv2w0z5MNuQ34130_assertion {
  miriam-gene:10735 a ncit:C16612 .
  lld:C0025202 a ncit:C7057 .
  dgn-gda:DGNfc8d100e32ee6392cd5577b06ae8dcd3 sio:SIO_000628 miriam-gene:10735 , lld:C0025202 ;
    a sio:SIO_001121 .
}
dgn-np:NP758639.RAn7Q2FHTJPalsb-Je_paSbH5kQ1LJE5zv2w0z5MNuQ34130_provenance {
  dgn-np:NP758639.RAn7Q2FHTJPalsb-Je_paSbH5kQ1LJE5zv2w0z5MNuQ34130_assertion dcterms:description "[STAG2 encodes a subunit of the cohesion complex that participates in mitotic chromatid separation and was recently found to show low expression and inactivating mutations in Ewing's sarcoma, melanoma and glioblastoma.In the childhood tumor neuroblastoma (NB) segmental chromosomal alterations are associated with poor prognosis whereas tumors displaying whole chromosome gains and losses have a much better prognosis.]. 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:24088605 ;
    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:NP758639.RAn7Q2FHTJPalsb-Je_paSbH5kQ1LJE5zv2w0z5MNuQ34130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:39+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" .
}