@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP447162.RADIkiD0ftrfBChQz-adgdsM8B27vLFommE--COtc0LJc> .
@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:NP447162.RADIkiD0ftrfBChQz-adgdsM8B27vLFommE--COtc0LJc130_head {
  this: np:hasAssertion dgn-np:NP447162.RADIkiD0ftrfBChQz-adgdsM8B27vLFommE--COtc0LJc130_assertion;
    np:hasProvenance dgn-np:NP447162.RADIkiD0ftrfBChQz-adgdsM8B27vLFommE--COtc0LJc130_provenance;
    np:hasPublicationInfo dgn-np:NP447162.RADIkiD0ftrfBChQz-adgdsM8B27vLFommE--COtc0LJc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP447162.RADIkiD0ftrfBChQz-adgdsM8B27vLFommE--COtc0LJc130_assertion a np:Assertion .
  
  dgn-np:NP447162.RADIkiD0ftrfBChQz-adgdsM8B27vLFommE--COtc0LJc130_provenance a np:Provenance .
  
  dgn-np:NP447162.RADIkiD0ftrfBChQz-adgdsM8B27vLFommE--COtc0LJc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP447162.RADIkiD0ftrfBChQz-adgdsM8B27vLFommE--COtc0LJc130_assertion {
  miriam-gene:3139 a ncit:C16612 .
  
  lld:C0043208 a ncit:C7057 .
  
  dgn-gda:DGNba61ec3ff6432cd3b260bc6ae96c26ea sio:SIO_000628 miriam-gene:3139, lld:C0043208;
    a sio:SIO_001121 .
}

dgn-np:NP447162.RADIkiD0ftrfBChQz-adgdsM8B27vLFommE--COtc0LJc130_provenance {
  dgn-np:NP447162.RADIkiD0ftrfBChQz-adgdsM8B27vLFommE--COtc0LJc130_assertion dcterms:description
      "[Mechanisms producing the divergent phenotypes, Wolman disease (WD) and cholesterol ester storage disease (CESD), associated with the genetic deficiency of human lysosomal acid lipase/cholesterol ester hydrolase (hLAL) function were investigated with the determination of HLAL activity levels, mRNA and protein expression, and defects in structural gene sequences in cells from three WD and five CESD 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:10562460;
    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:NP447162.RADIkiD0ftrfBChQz-adgdsM8B27vLFommE--COtc0LJc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:26+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" .
}