@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP224324.RAgj72oWclDrPV6lT7UADMPdN-XpRCyVMk9-evOkJ3juY> .
@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:NP224324.RAgj72oWclDrPV6lT7UADMPdN-XpRCyVMk9-evOkJ3juY130_head {
  this: np:hasAssertion dgn-np:NP224324.RAgj72oWclDrPV6lT7UADMPdN-XpRCyVMk9-evOkJ3juY130_assertion;
    np:hasProvenance dgn-np:NP224324.RAgj72oWclDrPV6lT7UADMPdN-XpRCyVMk9-evOkJ3juY130_provenance;
    np:hasPublicationInfo dgn-np:NP224324.RAgj72oWclDrPV6lT7UADMPdN-XpRCyVMk9-evOkJ3juY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP224324.RAgj72oWclDrPV6lT7UADMPdN-XpRCyVMk9-evOkJ3juY130_assertion a np:Assertion .
  
  dgn-np:NP224324.RAgj72oWclDrPV6lT7UADMPdN-XpRCyVMk9-evOkJ3juY130_provenance a np:Provenance .
  
  dgn-np:NP224324.RAgj72oWclDrPV6lT7UADMPdN-XpRCyVMk9-evOkJ3juY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP224324.RAgj72oWclDrPV6lT7UADMPdN-XpRCyVMk9-evOkJ3juY130_assertion {
  miriam-gene:51119 a ncit:C16612 .
  
  lld:C0497406 a ncit:C7057 .
  
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    a sio:SIO_001121 .
}

dgn-np:NP224324.RAgj72oWclDrPV6lT7UADMPdN-XpRCyVMk9-evOkJ3juY130_provenance {
  dgn-np:NP224324.RAgj72oWclDrPV6lT7UADMPdN-XpRCyVMk9-evOkJ3juY130_assertion dcterms:description
      "[Modelling the impact of different genotypes and their statistical interactions on SDS-BMI change adjusting for age, gender and baseline BMI or SDS-BMI, respectively, revealed that the combination of the CC genotype in INSIG2 and the AA genotype in FTO was significantly associated with the lowest degree of overweight reduction, but even with an increase in overweight (SDS-BMI change +0.51; 95% CI 0.22 to 0.79).]. 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:19224890;
    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:NP224324.RAgj72oWclDrPV6lT7UADMPdN-XpRCyVMk9-evOkJ3juY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:04+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}