@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP255486.RAYt9rAGDHqu0PPb1DGiGKqEVWV2I3HMujVngFr1Aul3s> .
@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/v3.0.0/void/> .

dgn-np:NP255486.RAYt9rAGDHqu0PPb1DGiGKqEVWV2I3HMujVngFr1Aul3s130_head {
  this: np:hasAssertion dgn-np:NP255486.RAYt9rAGDHqu0PPb1DGiGKqEVWV2I3HMujVngFr1Aul3s130_assertion;
    np:hasProvenance dgn-np:NP255486.RAYt9rAGDHqu0PPb1DGiGKqEVWV2I3HMujVngFr1Aul3s130_provenance;
    np:hasPublicationInfo dgn-np:NP255486.RAYt9rAGDHqu0PPb1DGiGKqEVWV2I3HMujVngFr1Aul3s130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP255486.RAYt9rAGDHqu0PPb1DGiGKqEVWV2I3HMujVngFr1Aul3s130_assertion a np:Assertion .
  
  dgn-np:NP255486.RAYt9rAGDHqu0PPb1DGiGKqEVWV2I3HMujVngFr1Aul3s130_provenance a np:Provenance .
  
  dgn-np:NP255486.RAYt9rAGDHqu0PPb1DGiGKqEVWV2I3HMujVngFr1Aul3s130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP255486.RAYt9rAGDHqu0PPb1DGiGKqEVWV2I3HMujVngFr1Aul3s130_assertion {
  miriam-gene:472 a ncit:C16612 .
  
  lld:C0242621 a ncit:C7057 .
  
  dgn-gda:DGN5a9048862c5ef4966e5d01ed5fe426a1 sio:SIO_000628 miriam-gene:472, lld:C0242621;
    a sio:SIO_001121 .
}

dgn-np:NP255486.RAYt9rAGDHqu0PPb1DGiGKqEVWV2I3HMujVngFr1Aul3s130_provenance {
  dgn-np:NP255486.RAYt9rAGDHqu0PPb1DGiGKqEVWV2I3HMujVngFr1Aul3s130_assertion dcterms:description
      "[Previous cytogenetic and molecular studies reported complex karyotypes with recurrent chromosomal abnormalities, including translocations involving either TCL1 at 14q32.1 or MTCP1 at Xq28, inactivation of the ATM gene by deletion and/or mutation, and isochromosomes 8.]. 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:11391795;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP255486.RAYt9rAGDHqu0PPb1DGiGKqEVWV2I3HMujVngFr1Aul3s130_publicationInfo {
  this: dcterms:created "2015-08-25T14:40:05+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}