@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP668176.RAjHRrfejjHQ2tdmmlOxRH3oBs4D7bzrIciPJYpFSl9x8> .
@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:NP668176.RAjHRrfejjHQ2tdmmlOxRH3oBs4D7bzrIciPJYpFSl9x8130_head {
  this: np:hasAssertion dgn-np:NP668176.RAjHRrfejjHQ2tdmmlOxRH3oBs4D7bzrIciPJYpFSl9x8130_assertion;
    np:hasProvenance dgn-np:NP668176.RAjHRrfejjHQ2tdmmlOxRH3oBs4D7bzrIciPJYpFSl9x8130_provenance;
    np:hasPublicationInfo dgn-np:NP668176.RAjHRrfejjHQ2tdmmlOxRH3oBs4D7bzrIciPJYpFSl9x8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP668176.RAjHRrfejjHQ2tdmmlOxRH3oBs4D7bzrIciPJYpFSl9x8130_assertion a np:Assertion .
  
  dgn-np:NP668176.RAjHRrfejjHQ2tdmmlOxRH3oBs4D7bzrIciPJYpFSl9x8130_provenance a np:Provenance .
  
  dgn-np:NP668176.RAjHRrfejjHQ2tdmmlOxRH3oBs4D7bzrIciPJYpFSl9x8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP668176.RAjHRrfejjHQ2tdmmlOxRH3oBs4D7bzrIciPJYpFSl9x8130_assertion {
  miriam-gene:57104 a ncit:C16612 .
  
  lld:C1853136 a ncit:C7057 .
  
  dgn-gda:DGN1bfb94eb0739ddf4ca0b19de0b82cf90 sio:SIO_000628 miriam-gene:57104, lld:C1853136;
    a sio:SIO_001121 .
}

dgn-np:NP668176.RAjHRrfejjHQ2tdmmlOxRH3oBs4D7bzrIciPJYpFSl9x8130_provenance {
  dgn-np:NP668176.RAjHRrfejjHQ2tdmmlOxRH3oBs4D7bzrIciPJYpFSl9x8130_assertion dcterms:description
      "[A subgroup of neutral lipid storage disease has been recently associated with myopathy (NLSDM) and attributed to mutations in the gene (PNPLA2) encoding an adipose triglyceride lipase involved in the degradation of intracellular triglycerides.]. 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:18952067;
    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:NP668176.RAjHRrfejjHQ2tdmmlOxRH3oBs4D7bzrIciPJYpFSl9x8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:43+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" .
}