@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP331782.RAweVZ8fbga3MeKrOonOqAbRV3NZY09An9FBCdOg6Yhuw> .
@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:NP331782.RAweVZ8fbga3MeKrOonOqAbRV3NZY09An9FBCdOg6Yhuw130_head {
  this: np:hasAssertion dgn-np:NP331782.RAweVZ8fbga3MeKrOonOqAbRV3NZY09An9FBCdOg6Yhuw130_assertion;
    np:hasProvenance dgn-np:NP331782.RAweVZ8fbga3MeKrOonOqAbRV3NZY09An9FBCdOg6Yhuw130_provenance;
    np:hasPublicationInfo dgn-np:NP331782.RAweVZ8fbga3MeKrOonOqAbRV3NZY09An9FBCdOg6Yhuw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP331782.RAweVZ8fbga3MeKrOonOqAbRV3NZY09An9FBCdOg6Yhuw130_assertion a np:Assertion .
  
  dgn-np:NP331782.RAweVZ8fbga3MeKrOonOqAbRV3NZY09An9FBCdOg6Yhuw130_provenance a np:Provenance .
  
  dgn-np:NP331782.RAweVZ8fbga3MeKrOonOqAbRV3NZY09An9FBCdOg6Yhuw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP331782.RAweVZ8fbga3MeKrOonOqAbRV3NZY09An9FBCdOg6Yhuw130_assertion {
  miriam-gene:3949 a ncit:C16612 .
  
  lld:C0154251 a ncit:C7057 .
  
  dgn-gda:DGN85baa28217521d4feb47d112fc64814f sio:SIO_000628 miriam-gene:3949, lld:C0154251;
    a sio:SIO_001121 .
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dgn-np:NP331782.RAweVZ8fbga3MeKrOonOqAbRV3NZY09An9FBCdOg6Yhuw130_provenance {
  dgn-np:NP331782.RAweVZ8fbga3MeKrOonOqAbRV3NZY09An9FBCdOg6Yhuw130_assertion dcterms:description
      "[These same molecular techniques have also been applied to pediatric lipid disorders with some notable successes, both in their diagnosis and understanding the mechanisms of the resulting pathology, including the recent experiments (Wilson JM, Grossman M, Wu CH, Chowdhury NR, Wu GY, Chowdhury JR: J Biol Chem 267:963-967, 1992) that have led to proposals to treat homozygous familial hypercholesterolemia by gene therapy.]. 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:8255668;
    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:NP331782.RAweVZ8fbga3MeKrOonOqAbRV3NZY09An9FBCdOg6Yhuw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:15+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>;
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    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
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