@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP44274.RAlyYsUYgC8KBYUkEgBeOVq6yg5rIgJAKqMFhODiu9UTI> .
@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 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:NP44274.RAlyYsUYgC8KBYUkEgBeOVq6yg5rIgJAKqMFhODiu9UTI130_head {
  this: np:hasAssertion dgn-np:NP44274.RAlyYsUYgC8KBYUkEgBeOVq6yg5rIgJAKqMFhODiu9UTI130_assertion;
    np:hasProvenance dgn-np:NP44274.RAlyYsUYgC8KBYUkEgBeOVq6yg5rIgJAKqMFhODiu9UTI130_provenance;
    np:hasPublicationInfo dgn-np:NP44274.RAlyYsUYgC8KBYUkEgBeOVq6yg5rIgJAKqMFhODiu9UTI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP44274.RAlyYsUYgC8KBYUkEgBeOVq6yg5rIgJAKqMFhODiu9UTI130_assertion a np:Assertion .
  
  dgn-np:NP44274.RAlyYsUYgC8KBYUkEgBeOVq6yg5rIgJAKqMFhODiu9UTI130_provenance a np:Provenance .
  
  dgn-np:NP44274.RAlyYsUYgC8KBYUkEgBeOVq6yg5rIgJAKqMFhODiu9UTI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP44274.RAlyYsUYgC8KBYUkEgBeOVq6yg5rIgJAKqMFhODiu9UTI130_assertion {
  miriam-gene:2169 a ncit:C16612 .
  
  lld:C0524620 a ncit:C7057 .
  
  dgn-gda:DGNb6c9942f5f72cbea6fd23b9083bcf206 sio:SIO_000628 miriam-gene:2169, lld:C0524620;
    a sio:SIO_001122 .
}

dgn-np:NP44274.RAlyYsUYgC8KBYUkEgBeOVq6yg5rIgJAKqMFhODiu9UTI130_provenance {
  dgn-np:NP44274.RAlyYsUYgC8KBYUkEgBeOVq6yg5rIgJAKqMFhODiu9UTI130_assertion dct:description
      "[We investigated the association of the A54T polymorphism of the FABP2 gene with the metabolic syndrome defined according to the diagnostic criteria recommended by the IDF in 2005, in our region (Marosvsrhely - Tg.]. 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:17383953;
    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:NP44274.RAlyYsUYgC8KBYUkEgBeOVq6yg5rIgJAKqMFhODiu9UTI130_publicationInfo {
  this: dct:created "2014-10-02T12:32:20+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}