@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP562044.RAH_RnRZFXLDVW07uGV6bYc_s_r5hJFP0WYEjXZfw74tU> .
@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:NP562044.RAH_RnRZFXLDVW07uGV6bYc_s_r5hJFP0WYEjXZfw74tU130_head {
  this: np:hasAssertion dgn-np:NP562044.RAH_RnRZFXLDVW07uGV6bYc_s_r5hJFP0WYEjXZfw74tU130_assertion ;
    np:hasProvenance dgn-np:NP562044.RAH_RnRZFXLDVW07uGV6bYc_s_r5hJFP0WYEjXZfw74tU130_provenance ;
    np:hasPublicationInfo dgn-np:NP562044.RAH_RnRZFXLDVW07uGV6bYc_s_r5hJFP0WYEjXZfw74tU130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP562044.RAH_RnRZFXLDVW07uGV6bYc_s_r5hJFP0WYEjXZfw74tU130_provenance a np:Provenance .
  dgn-np:NP562044.RAH_RnRZFXLDVW07uGV6bYc_s_r5hJFP0WYEjXZfw74tU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP562044.RAH_RnRZFXLDVW07uGV6bYc_s_r5hJFP0WYEjXZfw74tU130_assertion {
  miriam-gene:79068 a ncit:C16612 .
  lld:C0007222 a ncit:C7057 .
  dgn-gda:DGN21430664b118cc87b8002ef5c7827502 sio:SIO_000628 miriam-gene:79068 , lld:C0007222 ;
    a sio:SIO_001121 .
}
dgn-np:NP562044.RAH_RnRZFXLDVW07uGV6bYc_s_r5hJFP0WYEjXZfw74tU130_provenance {
  dgn-np:NP562044.RAH_RnRZFXLDVW07uGV6bYc_s_r5hJFP0WYEjXZfw74tU130_assertion dcterms:description "[To determine if FTO variants are associated with BMI in Old Order Amish (OOA) individuals, and to further determine whether the detrimental associations of FTO gene variants can be lessened by increased physical activity, a total of 704 healthy OOA adults were selected from the Heredity and Phenotype Intervention (HAPI) Heart Study, an investigation of gene x environment interactions in cardiovascular disease, for whom objective quantified physical activity measurements were available and for whom 92 single-nucleotide polymorphisms (SNPs) in FTO were genotyped.]. 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:18779467 ;
    prov:wasDerivedFrom dgn-void:befree-20140225 ;
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  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:NP562044.RAH_RnRZFXLDVW07uGV6bYc_s_r5hJFP0WYEjXZfw74tU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:39+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> ;
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