@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1410362.RAFLqz_uw1T0bcCtLkP9xwxOZK4Otz-hv4jKocy2k8_OI> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP1410362.RAFLqz_uw1T0bcCtLkP9xwxOZK4Otz-hv4jKocy2k8_OI130_head {
  this: np:hasAssertion dgn-np:NP1410362.RAFLqz_uw1T0bcCtLkP9xwxOZK4Otz-hv4jKocy2k8_OI130_assertion ;
    np:hasProvenance dgn-np:NP1410362.RAFLqz_uw1T0bcCtLkP9xwxOZK4Otz-hv4jKocy2k8_OI130_provenance ;
    np:hasPublicationInfo dgn-np:NP1410362.RAFLqz_uw1T0bcCtLkP9xwxOZK4Otz-hv4jKocy2k8_OI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP1410362.RAFLqz_uw1T0bcCtLkP9xwxOZK4Otz-hv4jKocy2k8_OI130_assertion a np:Assertion .
  dgn-np:NP1410362.RAFLqz_uw1T0bcCtLkP9xwxOZK4Otz-hv4jKocy2k8_OI130_provenance a np:Provenance .
  dgn-np:NP1410362.RAFLqz_uw1T0bcCtLkP9xwxOZK4Otz-hv4jKocy2k8_OI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP1410362.RAFLqz_uw1T0bcCtLkP9xwxOZK4Otz-hv4jKocy2k8_OI130_assertion {
  miriam-gene:3952 a ncit:C16612 .
  lld:C0028754 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP1410362.RAFLqz_uw1T0bcCtLkP9xwxOZK4Otz-hv4jKocy2k8_OI130_provenance {
  dgn-np:NP1410362.RAFLqz_uw1T0bcCtLkP9xwxOZK4Otz-hv4jKocy2k8_OI130_assertion dcterms:description "[We investigated whether an association exists between genetic variants of the human obesity (OB or leptin) gene and body mass index (BMI) or weight in subjects with Prader Willi syndrome (PWS) and in age- and gender-matched lean and obese subjects without PWS.]. 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:9842990 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1410362.RAFLqz_uw1T0bcCtLkP9xwxOZK4Otz-hv4jKocy2k8_OI130_publicationInfo {
  this: dcterms:created "2016-05-13T12:52:26+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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}