@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP48395.RAIOU1-x9WCkEHGh697wywo0BFtBQWr9R4c544PI_WRtM> .
@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:NP48395.RAIOU1-x9WCkEHGh697wywo0BFtBQWr9R4c544PI_WRtM130_head {
  this: np:hasAssertion dgn-np:NP48395.RAIOU1-x9WCkEHGh697wywo0BFtBQWr9R4c544PI_WRtM130_assertion;
    np:hasProvenance dgn-np:NP48395.RAIOU1-x9WCkEHGh697wywo0BFtBQWr9R4c544PI_WRtM130_provenance;
    np:hasPublicationInfo dgn-np:NP48395.RAIOU1-x9WCkEHGh697wywo0BFtBQWr9R4c544PI_WRtM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP48395.RAIOU1-x9WCkEHGh697wywo0BFtBQWr9R4c544PI_WRtM130_assertion a np:Assertion .
  
  dgn-np:NP48395.RAIOU1-x9WCkEHGh697wywo0BFtBQWr9R4c544PI_WRtM130_provenance a np:Provenance .
  
  dgn-np:NP48395.RAIOU1-x9WCkEHGh697wywo0BFtBQWr9R4c544PI_WRtM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP48395.RAIOU1-x9WCkEHGh697wywo0BFtBQWr9R4c544PI_WRtM130_assertion {
  miriam-gene:338 a ncit:C16612 .
  
  lld:C0020473 a ncit:C7057 .
  
  dgn-gda:DGNc78d5ca1dfb47aacae409fe53d7a4648 sio:SIO_000628 miriam-gene:338, lld:C0020473;
    a sio:SIO_001122 .
}

dgn-np:NP48395.RAIOU1-x9WCkEHGh697wywo0BFtBQWr9R4c544PI_WRtM130_provenance {
  dgn-np:NP48395.RAIOU1-x9WCkEHGh697wywo0BFtBQWr9R4c544PI_WRtM130_assertion dcterms:description
      "[We conclude that  this arginine 3500 is essential to the function of apoB and that its loss and replacement by glutamine or tryptophan is responsible for the hypercholesterolemia of familial defective apoB 100.]. 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:7627691;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP48395.RAIOU1-x9WCkEHGh697wywo0BFtBQWr9R4c544PI_WRtM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:22+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" .
}