@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP48298.RALtcMWktRd8RyFMfYkaWpL68qFI7SM8trnXBBVUFLEwk> .
@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:NP48298.RALtcMWktRd8RyFMfYkaWpL68qFI7SM8trnXBBVUFLEwk130_head {
  this: np:hasAssertion dgn-np:NP48298.RALtcMWktRd8RyFMfYkaWpL68qFI7SM8trnXBBVUFLEwk130_assertion;
    np:hasProvenance dgn-np:NP48298.RALtcMWktRd8RyFMfYkaWpL68qFI7SM8trnXBBVUFLEwk130_provenance;
    np:hasPublicationInfo dgn-np:NP48298.RALtcMWktRd8RyFMfYkaWpL68qFI7SM8trnXBBVUFLEwk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP48298.RALtcMWktRd8RyFMfYkaWpL68qFI7SM8trnXBBVUFLEwk130_assertion a np:Assertion .
  
  dgn-np:NP48298.RALtcMWktRd8RyFMfYkaWpL68qFI7SM8trnXBBVUFLEwk130_provenance a np:Provenance .
  
  dgn-np:NP48298.RALtcMWktRd8RyFMfYkaWpL68qFI7SM8trnXBBVUFLEwk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP48298.RALtcMWktRd8RyFMfYkaWpL68qFI7SM8trnXBBVUFLEwk130_assertion {
  miriam-gene:348 a ncit:C16612 .
  
  lld:C2673196 a ncit:C7057 .
  
  dgn-gda:DGN8abd94af49a97730abcee6100fa3e01e sio:SIO_000628 miriam-gene:348, lld:C2673196;
    a sio:SIO_001122 .
}

dgn-np:NP48298.RALtcMWktRd8RyFMfYkaWpL68qFI7SM8trnXBBVUFLEwk130_provenance {
  dgn-np:NP48298.RALtcMWktRd8RyFMfYkaWpL68qFI7SM8trnXBBVUFLEwk130_assertion dcterms:description
      "[ Apo E1 (Gln 156-Gly 173-->0) is a novel mutation of apo E that may be etiologically related to LPG and to the development of atherosclerosis. The result of this family study suggests that the occurrence of LPG may involve other genetic or environmental factors.]. 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:10504484;
    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:NP48298.RALtcMWktRd8RyFMfYkaWpL68qFI7SM8trnXBBVUFLEwk130_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" .
}