@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP761502.RAkt-JzwywMcq9W5pw6rqhJaLV6M_NYdgFhvAdOlocp34> .
@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:NP761502.RAkt-JzwywMcq9W5pw6rqhJaLV6M_NYdgFhvAdOlocp34130_head {
  this: np:hasAssertion dgn-np:NP761502.RAkt-JzwywMcq9W5pw6rqhJaLV6M_NYdgFhvAdOlocp34130_assertion;
    np:hasProvenance dgn-np:NP761502.RAkt-JzwywMcq9W5pw6rqhJaLV6M_NYdgFhvAdOlocp34130_provenance;
    np:hasPublicationInfo dgn-np:NP761502.RAkt-JzwywMcq9W5pw6rqhJaLV6M_NYdgFhvAdOlocp34130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP761502.RAkt-JzwywMcq9W5pw6rqhJaLV6M_NYdgFhvAdOlocp34130_assertion a np:Assertion .
  
  dgn-np:NP761502.RAkt-JzwywMcq9W5pw6rqhJaLV6M_NYdgFhvAdOlocp34130_provenance a np:Provenance .
  
  dgn-np:NP761502.RAkt-JzwywMcq9W5pw6rqhJaLV6M_NYdgFhvAdOlocp34130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP761502.RAkt-JzwywMcq9W5pw6rqhJaLV6M_NYdgFhvAdOlocp34130_assertion {
  miriam-gene:6281 a ncit:C16612 .
  
  lld:C0795875 a ncit:C7057 .
  
  dgn-gda:DGN121a8ace23285a44486c0b67ae6361ed sio:SIO_000628 miriam-gene:6281, lld:C0795875;
    a sio:SIO_001121 .
}

dgn-np:NP761502.RAkt-JzwywMcq9W5pw6rqhJaLV6M_NYdgFhvAdOlocp34130_provenance {
  dgn-np:NP761502.RAkt-JzwywMcq9W5pw6rqhJaLV6M_NYdgFhvAdOlocp34130_assertion dcterms:description
      "[Five abnormalities were designated as clonal (monosomy 21 in three metaphases and 64 approximately 69,XXY in three metaphases from one patient at different times, and del(20)(q12q13) in three metaphases, add(13)(q34) in two metaphases, and ?del(19)(p11) in two metaphases from three different patients).]. 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:10731583;
    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:NP761502.RAkt-JzwywMcq9W5pw6rqhJaLV6M_NYdgFhvAdOlocp34130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:41+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" .
}