@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP747358.RAVCDG_lzr0lbB31p1Y81CuMUsypMenKnYHaX2S-VoSjM> .
@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:NP747358.RAVCDG_lzr0lbB31p1Y81CuMUsypMenKnYHaX2S-VoSjM130_head {
  this: np:hasAssertion dgn-np:NP747358.RAVCDG_lzr0lbB31p1Y81CuMUsypMenKnYHaX2S-VoSjM130_assertion;
    np:hasProvenance dgn-np:NP747358.RAVCDG_lzr0lbB31p1Y81CuMUsypMenKnYHaX2S-VoSjM130_provenance;
    np:hasPublicationInfo dgn-np:NP747358.RAVCDG_lzr0lbB31p1Y81CuMUsypMenKnYHaX2S-VoSjM130_publicationInfo;
    a np:Nanopublication .
  
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  dgn-np:NP747358.RAVCDG_lzr0lbB31p1Y81CuMUsypMenKnYHaX2S-VoSjM130_provenance a np:Provenance .
  
  dgn-np:NP747358.RAVCDG_lzr0lbB31p1Y81CuMUsypMenKnYHaX2S-VoSjM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP747358.RAVCDG_lzr0lbB31p1Y81CuMUsypMenKnYHaX2S-VoSjM130_assertion {
  miriam-gene:4852 a ncit:C16612 .
  
  lld:C0007222 a ncit:C7057 .
  
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    a sio:SIO_001121 .
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dgn-np:NP747358.RAVCDG_lzr0lbB31p1Y81CuMUsypMenKnYHaX2S-VoSjM130_provenance {
  dgn-np:NP747358.RAVCDG_lzr0lbB31p1Y81CuMUsypMenKnYHaX2S-VoSjM130_assertion dcterms:description
      "[The objective of the present study was to evaluate the association of single nucleotide polymorphisms (SNPs) in the NPY gene with obesity, metabolic syndrome features, and inflammatory and cardiovascular disease (CVD) risk biomarkers in Spanish children.]. 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:23624317;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP747358.RAVCDG_lzr0lbB31p1Y81CuMUsypMenKnYHaX2S-VoSjM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:33+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;
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    pav:version "v2.1.0.0" .
  
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