@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP282250.RA8GU8w_bffbThhovL0zyiRmuNtktPSR6WizHdQpLNvHg> .
@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:NP282250.RA8GU8w_bffbThhovL0zyiRmuNtktPSR6WizHdQpLNvHg130_head {
  this: np:hasAssertion dgn-np:NP282250.RA8GU8w_bffbThhovL0zyiRmuNtktPSR6WizHdQpLNvHg130_assertion;
    np:hasProvenance dgn-np:NP282250.RA8GU8w_bffbThhovL0zyiRmuNtktPSR6WizHdQpLNvHg130_provenance;
    np:hasPublicationInfo dgn-np:NP282250.RA8GU8w_bffbThhovL0zyiRmuNtktPSR6WizHdQpLNvHg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP282250.RA8GU8w_bffbThhovL0zyiRmuNtktPSR6WizHdQpLNvHg130_assertion a np:Assertion .
  
  dgn-np:NP282250.RA8GU8w_bffbThhovL0zyiRmuNtktPSR6WizHdQpLNvHg130_provenance a np:Provenance .
  
  dgn-np:NP282250.RA8GU8w_bffbThhovL0zyiRmuNtktPSR6WizHdQpLNvHg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP282250.RA8GU8w_bffbThhovL0zyiRmuNtktPSR6WizHdQpLNvHg130_assertion {
  miriam-gene:118429 a ncit:C16612 .
  
  lld:C0220620 a ncit:C7057 .
  
  dgn-gda:DGN997194e832c6eb63e903757cff6fd0c7 sio:SIO_000628 miriam-gene:118429, lld:C0220620;
    a sio:SIO_001121 .
}

dgn-np:NP282250.RA8GU8w_bffbThhovL0zyiRmuNtktPSR6WizHdQpLNvHg130_provenance {
  dgn-np:NP282250.RA8GU8w_bffbThhovL0zyiRmuNtktPSR6WizHdQpLNvHg130_assertion dcterms:description
      "[We have performed in situ hybridization (ISH) studies on paraffin sections and on isolated nuclei of 13 pediatric GCT with particular emphasis on those chromosome abnormalities that are common in adult GCT.]. 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:7529045;
    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:NP282250.RA8GU8w_bffbThhovL0zyiRmuNtktPSR6WizHdQpLNvHg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:39+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" .
}