@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1046239.RAnQv4n1Fu6-fE6KdqQeTBjkSdy_xg4_Ufv5bxVyhFPUQ> .
@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:NP1046239.RAnQv4n1Fu6-fE6KdqQeTBjkSdy_xg4_Ufv5bxVyhFPUQ130_head {
  this: np:hasAssertion dgn-np:NP1046239.RAnQv4n1Fu6-fE6KdqQeTBjkSdy_xg4_Ufv5bxVyhFPUQ130_assertion;
    np:hasProvenance dgn-np:NP1046239.RAnQv4n1Fu6-fE6KdqQeTBjkSdy_xg4_Ufv5bxVyhFPUQ130_provenance;
    np:hasPublicationInfo dgn-np:NP1046239.RAnQv4n1Fu6-fE6KdqQeTBjkSdy_xg4_Ufv5bxVyhFPUQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1046239.RAnQv4n1Fu6-fE6KdqQeTBjkSdy_xg4_Ufv5bxVyhFPUQ130_assertion a np:Assertion .
  
  dgn-np:NP1046239.RAnQv4n1Fu6-fE6KdqQeTBjkSdy_xg4_Ufv5bxVyhFPUQ130_provenance a np:Provenance .
  
  dgn-np:NP1046239.RAnQv4n1Fu6-fE6KdqQeTBjkSdy_xg4_Ufv5bxVyhFPUQ130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1046239.RAnQv4n1Fu6-fE6KdqQeTBjkSdy_xg4_Ufv5bxVyhFPUQ130_assertion {
  miriam-gene:2688 a ncit:C16612 .
  
  lld:C0028754 a ncit:C7057 .
  
  dgn-gda:DGNf77c0c01ca61015ddfa635623db05f32 sio:SIO_000628 miriam-gene:2688, lld:C0028754;
    a sio:SIO_001121 .
}

dgn-np:NP1046239.RAnQv4n1Fu6-fE6KdqQeTBjkSdy_xg4_Ufv5bxVyhFPUQ130_provenance {
  dgn-np:NP1046239.RAnQv4n1Fu6-fE6KdqQeTBjkSdy_xg4_Ufv5bxVyhFPUQ130_assertion dcterms:description
      "[This neural defect, together with increased fat mass, blunted circadian rhythm, and growth hormone response pathway defects that are also linked to loss of MAGEL2, could contribute to the hyperphagia and obesity that are hallmarks of this disorder.]. 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:23341784;
    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:NP1046239.RAnQv4n1Fu6-fE6KdqQeTBjkSdy_xg4_Ufv5bxVyhFPUQ130_publicationInfo {
  this: dcterms:created "2016-05-13T12:49:40+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:disgenetv3.0rdf;
    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>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}