@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP751905.RAp3jc9xSmb2oKqUYydqHX1N6Iw-eJqhplCHbSOXD65g8> .
@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:NP751905.RAp3jc9xSmb2oKqUYydqHX1N6Iw-eJqhplCHbSOXD65g8130_head {
  this: np:hasAssertion dgn-np:NP751905.RAp3jc9xSmb2oKqUYydqHX1N6Iw-eJqhplCHbSOXD65g8130_assertion;
    np:hasProvenance dgn-np:NP751905.RAp3jc9xSmb2oKqUYydqHX1N6Iw-eJqhplCHbSOXD65g8130_provenance;
    np:hasPublicationInfo dgn-np:NP751905.RAp3jc9xSmb2oKqUYydqHX1N6Iw-eJqhplCHbSOXD65g8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP751905.RAp3jc9xSmb2oKqUYydqHX1N6Iw-eJqhplCHbSOXD65g8130_assertion a np:Assertion .
  
  dgn-np:NP751905.RAp3jc9xSmb2oKqUYydqHX1N6Iw-eJqhplCHbSOXD65g8130_provenance a np:Provenance .
  
  dgn-np:NP751905.RAp3jc9xSmb2oKqUYydqHX1N6Iw-eJqhplCHbSOXD65g8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP751905.RAp3jc9xSmb2oKqUYydqHX1N6Iw-eJqhplCHbSOXD65g8130_assertion {
  miriam-gene:6616 a ncit:C16612 .
  
  lld:C0004135 a ncit:C7057 .
  
  dgn-gda:DGN44a1157201e1421e5103d6a3afda2d3a sio:SIO_000628 miriam-gene:6616, lld:C0004135;
    a sio:SIO_001121 .
}

dgn-np:NP751905.RAp3jc9xSmb2oKqUYydqHX1N6Iw-eJqhplCHbSOXD65g8130_provenance {
  dgn-np:NP751905.RAp3jc9xSmb2oKqUYydqHX1N6Iw-eJqhplCHbSOXD65g8130_assertion dcterms:description
      "[The distal breakpoint of inv(14) in T cell clones, established from patients with ataxia telangiectasia, lies outside the immunoglobulin heavy chain gene locus on 14q32.3, and more proximal to the centromere than the distal breakpoint of inv(14) in the T cell lymphoma cell line SUP-T1.]. 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:2358304;
    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:NP751905.RAp3jc9xSmb2oKqUYydqHX1N6Iw-eJqhplCHbSOXD65g8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:35+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" .
}