@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP85099.RAnJ6gK1pb5IvUb9rIvQfoo8CuxrsxLxnmyvInanbUeso> .
@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:NP85099.RAnJ6gK1pb5IvUb9rIvQfoo8CuxrsxLxnmyvInanbUeso130_head {
  this: np:hasAssertion dgn-np:NP85099.RAnJ6gK1pb5IvUb9rIvQfoo8CuxrsxLxnmyvInanbUeso130_assertion;
    np:hasProvenance dgn-np:NP85099.RAnJ6gK1pb5IvUb9rIvQfoo8CuxrsxLxnmyvInanbUeso130_provenance;
    np:hasPublicationInfo dgn-np:NP85099.RAnJ6gK1pb5IvUb9rIvQfoo8CuxrsxLxnmyvInanbUeso130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP85099.RAnJ6gK1pb5IvUb9rIvQfoo8CuxrsxLxnmyvInanbUeso130_assertion a np:Assertion .
  
  dgn-np:NP85099.RAnJ6gK1pb5IvUb9rIvQfoo8CuxrsxLxnmyvInanbUeso130_provenance a np:Provenance .
  
  dgn-np:NP85099.RAnJ6gK1pb5IvUb9rIvQfoo8CuxrsxLxnmyvInanbUeso130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP85099.RAnJ6gK1pb5IvUb9rIvQfoo8CuxrsxLxnmyvInanbUeso130_assertion {
  miriam-gene:3953 a ncit:C16612 .
  
  lld:C0162739 a ncit:C7057 .
  
  dgn-gda:DGN33a0f902b1c4ba81c8a5d3377e75672e sio:SIO_000628 miriam-gene:3953, lld:C0162739;
    a sio:SIO_001122 .
}

dgn-np:NP85099.RAnJ6gK1pb5IvUb9rIvQfoo8CuxrsxLxnmyvInanbUeso130_provenance {
  dgn-np:NP85099.RAnJ6gK1pb5IvUb9rIvQfoo8CuxrsxLxnmyvInanbUeso130_assertion dcterms:description
      "[Although certain LEPR haplotypes are more frequent in HELLP syndrome, we conclude that there is no compelling evidence that the four studied LEPR SNP polymorphisms associated with the development of HELLP syndrome.]. 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:20149225;
    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:NP85099.RAnJ6gK1pb5IvUb9rIvQfoo8CuxrsxLxnmyvInanbUeso130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:42+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" .
}