@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP372295.RAPuDwK8nM4iSv_fek7zBJycpCayAfcBj9JgAcbZ7IJ-g> .
@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:NP372295.RAPuDwK8nM4iSv_fek7zBJycpCayAfcBj9JgAcbZ7IJ-g130_head {
  this: np:hasAssertion dgn-np:NP372295.RAPuDwK8nM4iSv_fek7zBJycpCayAfcBj9JgAcbZ7IJ-g130_assertion;
    np:hasProvenance dgn-np:NP372295.RAPuDwK8nM4iSv_fek7zBJycpCayAfcBj9JgAcbZ7IJ-g130_provenance;
    np:hasPublicationInfo dgn-np:NP372295.RAPuDwK8nM4iSv_fek7zBJycpCayAfcBj9JgAcbZ7IJ-g130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP372295.RAPuDwK8nM4iSv_fek7zBJycpCayAfcBj9JgAcbZ7IJ-g130_assertion a np:Assertion .
  
  dgn-np:NP372295.RAPuDwK8nM4iSv_fek7zBJycpCayAfcBj9JgAcbZ7IJ-g130_provenance a np:Provenance .
  
  dgn-np:NP372295.RAPuDwK8nM4iSv_fek7zBJycpCayAfcBj9JgAcbZ7IJ-g130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP372295.RAPuDwK8nM4iSv_fek7zBJycpCayAfcBj9JgAcbZ7IJ-g130_assertion {
  miriam-gene:4023 a ncit:C16612 .
  
  lld:C0008626 a ncit:C7057 .
  
  dgn-gda:DGN0cef32bda86f15449a97bf3596f4dde1 sio:SIO_000628 miriam-gene:4023, lld:C0008626;
    a sio:SIO_001121 .
}

dgn-np:NP372295.RAPuDwK8nM4iSv_fek7zBJycpCayAfcBj9JgAcbZ7IJ-g130_provenance {
  dgn-np:NP372295.RAPuDwK8nM4iSv_fek7zBJycpCayAfcBj9JgAcbZ7IJ-g130_assertion dcterms:description
      "[Higher LPL level was found in patients with unfavorable cytogenetic aberrations (deletion in 17p13 or 11q22) in contrast to lower level in good risk cytogenetics (deletion in 13q as the sole abnormality) (r = 0.404, P = 0.002).]. 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:18616755;
    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:NP372295.RAPuDwK8nM4iSv_fek7zBJycpCayAfcBj9JgAcbZ7IJ-g130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:38+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" .
}