@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP48310.RAIrhd9YyUtate9-DZz9yxZoCt3X7w7dRGavdiLb8pjK4> .
@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:NP48310.RAIrhd9YyUtate9-DZz9yxZoCt3X7w7dRGavdiLb8pjK4130_head {
  this: np:hasAssertion dgn-np:NP48310.RAIrhd9YyUtate9-DZz9yxZoCt3X7w7dRGavdiLb8pjK4130_assertion ;
    np:hasProvenance dgn-np:NP48310.RAIrhd9YyUtate9-DZz9yxZoCt3X7w7dRGavdiLb8pjK4130_provenance ;
    np:hasPublicationInfo dgn-np:NP48310.RAIrhd9YyUtate9-DZz9yxZoCt3X7w7dRGavdiLb8pjK4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP48310.RAIrhd9YyUtate9-DZz9yxZoCt3X7w7dRGavdiLb8pjK4130_assertion a np:Assertion .
  dgn-np:NP48310.RAIrhd9YyUtate9-DZz9yxZoCt3X7w7dRGavdiLb8pjK4130_provenance a np:Provenance .
  dgn-np:NP48310.RAIrhd9YyUtate9-DZz9yxZoCt3X7w7dRGavdiLb8pjK4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP48310.RAIrhd9YyUtate9-DZz9yxZoCt3X7w7dRGavdiLb8pjK4130_assertion {
  miriam-gene:348 a ncit:C16612 .
  lld:C0032914 a ncit:C7057 .
  dgn-gda:DGN7dd6f5cda721398c121e4c7fe43d4f38 sio:SIO_000628 miriam-gene:348 , lld:C0032914 ;
    a sio:SIO_001122 .
}
dgn-np:NP48310.RAIrhd9YyUtate9-DZz9yxZoCt3X7w7dRGavdiLb8pjK4130_provenance {
  dgn-np:NP48310.RAIrhd9YyUtate9-DZz9yxZoCt3X7w7dRGavdiLb8pjK4130_assertion dcterms:description "[ We were unable to demonstrate that the atherogenic state of preeclampsia is associated with a particular genotype of apo E. Familial studies show that shared genetic and environmental factors are involved in lipid variability. However, owing to the diversity of factors contributing to the development of preeclampsia (fetal and paternal genotypes), these data do not allow to rule-out a possible contribution of maternal apo E to preeclampsia.]. 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:12175441 ;
    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:NP48310.RAIrhd9YyUtate9-DZz9yxZoCt3X7w7dRGavdiLb8pjK4130_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" .
}