@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP244353.RAgs34eDLLgSapC9aws7-E8U8eQWmhFhkh2Mdfwek3nAw> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .
dgn-np:NP244353.RAgs34eDLLgSapC9aws7-E8U8eQWmhFhkh2Mdfwek3nAw130_head {
   this: np:hasAssertion dgn-np:NP244353.RAgs34eDLLgSapC9aws7-E8U8eQWmhFhkh2Mdfwek3nAw130_assertion ;
    np:hasProvenance dgn-np:NP244353.RAgs34eDLLgSapC9aws7-E8U8eQWmhFhkh2Mdfwek3nAw130_provenance ;
    np:hasPublicationInfo dgn-np:NP244353.RAgs34eDLLgSapC9aws7-E8U8eQWmhFhkh2Mdfwek3nAw130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP244353.RAgs34eDLLgSapC9aws7-E8U8eQWmhFhkh2Mdfwek3nAw130_assertion a np:Assertion .
  dgn-np:NP244353.RAgs34eDLLgSapC9aws7-E8U8eQWmhFhkh2Mdfwek3nAw130_provenance a np:Provenance .
  dgn-np:NP244353.RAgs34eDLLgSapC9aws7-E8U8eQWmhFhkh2Mdfwek3nAw130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP244353.RAgs34eDLLgSapC9aws7-E8U8eQWmhFhkh2Mdfwek3nAw130_assertion {
   miriam-gene:344 a ncit:C16612 .
  lld:C0020445 a ncit:C7057 .
  dgn-gda:DGN9e09913c43e8afd8d5850a8a8836385a sio:SIO_000628 miriam-gene:344 , lld:C0020445 ;
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dgn-np:NP244353.RAgs34eDLLgSapC9aws7-E8U8eQWmhFhkh2Mdfwek3nAw130_provenance {
   dgn-np:NP244353.RAgs34eDLLgSapC9aws7-E8U8eQWmhFhkh2Mdfwek3nAw130_assertion dcterms:description "[The purpose of this review is to detail this molecular genetic progress for two of the disorders that result in disturbed triglyceride metabolism in infants, lipoprotein lipase deficiency and apo CII deficiency, and four disorders that lead to disturbed cholesterol levels in infancy, abetalipoproteinemia, hypobetalipoproteinemia, familial defective apo B, and familial hypercholesterolemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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    sio:SIO_000772 miriam-pubmed:8255668 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
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  dgn-void:source_evidence_literature a eco:ECO_0000212 ;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
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}
dgn-np:NP244353.RAgs34eDLLgSapC9aws7-E8U8eQWmhFhkh2Mdfwek3nAw130_publicationInfo {
   this: dcterms:created "2015-08-25T14:39:59+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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}