@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP286583.RAmFwAP398bsFxpl_oT3gRStq0HoR2wVn6XRxlnnL9Ur0> .
@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:NP286583.RAmFwAP398bsFxpl_oT3gRStq0HoR2wVn6XRxlnnL9Ur0130_head {
  this: np:hasAssertion dgn-np:NP286583.RAmFwAP398bsFxpl_oT3gRStq0HoR2wVn6XRxlnnL9Ur0130_assertion;
    np:hasProvenance dgn-np:NP286583.RAmFwAP398bsFxpl_oT3gRStq0HoR2wVn6XRxlnnL9Ur0130_provenance;
    np:hasPublicationInfo dgn-np:NP286583.RAmFwAP398bsFxpl_oT3gRStq0HoR2wVn6XRxlnnL9Ur0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP286583.RAmFwAP398bsFxpl_oT3gRStq0HoR2wVn6XRxlnnL9Ur0130_assertion a np:Assertion .
  
  dgn-np:NP286583.RAmFwAP398bsFxpl_oT3gRStq0HoR2wVn6XRxlnnL9Ur0130_provenance a np:Provenance .
  
  dgn-np:NP286583.RAmFwAP398bsFxpl_oT3gRStq0HoR2wVn6XRxlnnL9Ur0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP286583.RAmFwAP398bsFxpl_oT3gRStq0HoR2wVn6XRxlnnL9Ur0130_assertion {
  miriam-gene:51738 a ncit:C16612 .
  
  lld:C0524620 a ncit:C7057 .
  
  dgn-gda:DGN040b2dae7a864d15d635d2ed524e746b sio:SIO_000628 miriam-gene:51738, lld:C0524620;
    a sio:SIO_001121 .
}

dgn-np:NP286583.RAmFwAP398bsFxpl_oT3gRStq0HoR2wVn6XRxlnnL9Ur0130_provenance {
  dgn-np:NP286583.RAmFwAP398bsFxpl_oT3gRStq0HoR2wVn6XRxlnnL9Ur0130_assertion dcterms:description
      "[We genotyped 856 Amish samples for three missense polymorphisms in GHRL, Arg51Gln, Leu72Met (rs696217), and Gln90Leu (rs4684677) and performed association analyses with eating behavior traits and metabolic syndrome as defined by the National Cholesterol Education Program Adult Treatment Panel III guidelines.]. 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:16204371;
    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:NP286583.RAmFwAP398bsFxpl_oT3gRStq0HoR2wVn6XRxlnnL9Ur0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:43+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" .
}