@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP53067.RAiV7FEmviWnVBjzvm03crLzLAq8pHWnu7EPRb2lvby6U> .
@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:NP53067.RAiV7FEmviWnVBjzvm03crLzLAq8pHWnu7EPRb2lvby6U130_head {
  this: np:hasAssertion dgn-np:NP53067.RAiV7FEmviWnVBjzvm03crLzLAq8pHWnu7EPRb2lvby6U130_assertion ;
    np:hasProvenance dgn-np:NP53067.RAiV7FEmviWnVBjzvm03crLzLAq8pHWnu7EPRb2lvby6U130_provenance ;
    np:hasPublicationInfo dgn-np:NP53067.RAiV7FEmviWnVBjzvm03crLzLAq8pHWnu7EPRb2lvby6U130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP53067.RAiV7FEmviWnVBjzvm03crLzLAq8pHWnu7EPRb2lvby6U130_assertion a np:Assertion .
  dgn-np:NP53067.RAiV7FEmviWnVBjzvm03crLzLAq8pHWnu7EPRb2lvby6U130_provenance a np:Provenance .
  dgn-np:NP53067.RAiV7FEmviWnVBjzvm03crLzLAq8pHWnu7EPRb2lvby6U130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP53067.RAiV7FEmviWnVBjzvm03crLzLAq8pHWnu7EPRb2lvby6U130_assertion {
  miriam-gene:5360 a ncit:C16612 .
  lld:C0028754 a ncit:C7057 .
  dgn-gda:DGN59eecdaacb9663dca84f35ffd1dfe08c sio:SIO_000628 miriam-gene:5360 , lld:C0028754 ;
    a sio:SIO_001122 .
}
dgn-np:NP53067.RAiV7FEmviWnVBjzvm03crLzLAq8pHWnu7EPRb2lvby6U130_provenance {
  dgn-np:NP53067.RAiV7FEmviWnVBjzvm03crLzLAq8pHWnu7EPRb2lvby6U130_assertion dcterms:description "[ Intronic variants of the PLTP gene are significantly associated with obesity-related phenotypes. Considering the number and the relevance of candidate genes surrounding the PLTP locus and the absence of missense polymorphisms in the coding region, the associations could be mediated by a second gene allele in linkage disequilibrium with the marker locus.]. 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:15953936 ;
    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:NP53067.RAiV7FEmviWnVBjzvm03crLzLAq8pHWnu7EPRb2lvby6U130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:24+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" .
}