@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP335304.RAuVhvAZVRZqP1ve9FEGtF0eU6iHAeiKdHEb0h5gfPzdo> .
@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:NP335304.RAuVhvAZVRZqP1ve9FEGtF0eU6iHAeiKdHEb0h5gfPzdo130_head {
  this: np:hasAssertion dgn-np:NP335304.RAuVhvAZVRZqP1ve9FEGtF0eU6iHAeiKdHEb0h5gfPzdo130_assertion;
    np:hasProvenance dgn-np:NP335304.RAuVhvAZVRZqP1ve9FEGtF0eU6iHAeiKdHEb0h5gfPzdo130_provenance;
    np:hasPublicationInfo dgn-np:NP335304.RAuVhvAZVRZqP1ve9FEGtF0eU6iHAeiKdHEb0h5gfPzdo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP335304.RAuVhvAZVRZqP1ve9FEGtF0eU6iHAeiKdHEb0h5gfPzdo130_assertion a np:Assertion .
  
  dgn-np:NP335304.RAuVhvAZVRZqP1ve9FEGtF0eU6iHAeiKdHEb0h5gfPzdo130_provenance a np:Provenance .
  
  dgn-np:NP335304.RAuVhvAZVRZqP1ve9FEGtF0eU6iHAeiKdHEb0h5gfPzdo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP335304.RAuVhvAZVRZqP1ve9FEGtF0eU6iHAeiKdHEb0h5gfPzdo130_assertion {
  miriam-gene:3492 a ncit:C16612 .
  
  lld:C0007120 a ncit:C7057 .
  
  dgn-gda:DGN2df7f4069c68851096df8f24318af7a2 sio:SIO_000628 miriam-gene:3492, lld:C0007120;
    a sio:SIO_001121 .
}

dgn-np:NP335304.RAuVhvAZVRZqP1ve9FEGtF0eU6iHAeiKdHEb0h5gfPzdo130_provenance {
  dgn-np:NP335304.RAuVhvAZVRZqP1ve9FEGtF0eU6iHAeiKdHEb0h5gfPzdo130_assertion dcterms:description
      "[Although Southern blotting with derived genomic 6p21.1 probes failed to detect other rearrangements, fluorescent in situ hybridization assays, using BAC (bacterial artificial chromosome) clones spanning and flanking the CCND3 locus, along with probes for IGH confirmed localization of 6p21.1 breakpoints within the same region, as well as fusion of the CCND3 and IGH loci.]. 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:11675358;
    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:NP335304.RAuVhvAZVRZqP1ve9FEGtF0eU6iHAeiKdHEb0h5gfPzdo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:17+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" .
}