@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP719880.RAGEymoxNjkiIxvxi3SLoNDhmHu3pzcZfbzru7AydWNOI> .
@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:NP719880.RAGEymoxNjkiIxvxi3SLoNDhmHu3pzcZfbzru7AydWNOI130_head {
   this: np:hasAssertion dgn-np:NP719880.RAGEymoxNjkiIxvxi3SLoNDhmHu3pzcZfbzru7AydWNOI130_assertion ;
    np:hasProvenance dgn-np:NP719880.RAGEymoxNjkiIxvxi3SLoNDhmHu3pzcZfbzru7AydWNOI130_provenance ;
    np:hasPublicationInfo dgn-np:NP719880.RAGEymoxNjkiIxvxi3SLoNDhmHu3pzcZfbzru7AydWNOI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP719880.RAGEymoxNjkiIxvxi3SLoNDhmHu3pzcZfbzru7AydWNOI130_assertion a np:Assertion .
  dgn-np:NP719880.RAGEymoxNjkiIxvxi3SLoNDhmHu3pzcZfbzru7AydWNOI130_provenance a np:Provenance .
  dgn-np:NP719880.RAGEymoxNjkiIxvxi3SLoNDhmHu3pzcZfbzru7AydWNOI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP719880.RAGEymoxNjkiIxvxi3SLoNDhmHu3pzcZfbzru7AydWNOI130_assertion {
   miriam-gene:2693 a ncit:C16612 .
  lld:C0013473 a ncit:C7057 .
  dgn-gda:DGN86b9d5960d9c540d8f4190fca5b59eb0 sio:SIO_000628 miriam-gene:2693 , lld:C0013473 ;
    a sio:SIO_001121 .
}
dgn-np:NP719880.RAGEymoxNjkiIxvxi3SLoNDhmHu3pzcZfbzru7AydWNOI130_provenance {
   dgn-np:NP719880.RAGEymoxNjkiIxvxi3SLoNDhmHu3pzcZfbzru7AydWNOI130_assertion dcterms:description "[Genetic variants of ghrelin, an endogenous acylated peptide that stimulates growth hormone secretion, enhances appetite, and increases body weight, have been investigated in association with eating disorders, as changes in the ghrelin/growth hormone secretagogue receptor (GHSR)/ghrelin O-acyltransferase (GOAT) system have been implicated in its pathology.]. 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:23601422 ;
    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:NP719880.RAGEymoxNjkiIxvxi3SLoNDhmHu3pzcZfbzru7AydWNOI130_publicationInfo {
   this: dcterms:created "2014-10-02T12:39:17+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> ;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}