@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP160172.RAU4NM98yd1mjz6FmDsawOj9iwRaEXn5FH_fw-i19CWrM> .
@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:NP160172.RAU4NM98yd1mjz6FmDsawOj9iwRaEXn5FH_fw-i19CWrM130_head {
  this: np:hasAssertion dgn-np:NP160172.RAU4NM98yd1mjz6FmDsawOj9iwRaEXn5FH_fw-i19CWrM130_assertion;
    np:hasProvenance dgn-np:NP160172.RAU4NM98yd1mjz6FmDsawOj9iwRaEXn5FH_fw-i19CWrM130_provenance;
    np:hasPublicationInfo dgn-np:NP160172.RAU4NM98yd1mjz6FmDsawOj9iwRaEXn5FH_fw-i19CWrM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP160172.RAU4NM98yd1mjz6FmDsawOj9iwRaEXn5FH_fw-i19CWrM130_assertion a np:Assertion .
  
  dgn-np:NP160172.RAU4NM98yd1mjz6FmDsawOj9iwRaEXn5FH_fw-i19CWrM130_provenance a np:Provenance .
  
  dgn-np:NP160172.RAU4NM98yd1mjz6FmDsawOj9iwRaEXn5FH_fw-i19CWrM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP160172.RAU4NM98yd1mjz6FmDsawOj9iwRaEXn5FH_fw-i19CWrM130_assertion {
  miriam-gene:2693 a ncit:C16612 .
  
  lld:C0028754 a ncit:C7057 .
  
  dgn-gda:DGNebf5ce9325578d827a24e0bb8900105b sio:SIO_000628 miriam-gene:2693, lld:C0028754;
    a sio:SIO_001121 .
}

dgn-np:NP160172.RAU4NM98yd1mjz6FmDsawOj9iwRaEXn5FH_fw-i19CWrM130_provenance {
  dgn-np:NP160172.RAU4NM98yd1mjz6FmDsawOj9iwRaEXn5FH_fw-i19CWrM130_assertion dcterms:description
      "[This linkage, together with significant transmission disequilibrium in families and replication of this association in an independent population, provides evidence that common SNPs and haplotypes within the GHSR region are involved in the pathogenesis of human obesity.]. 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:15616037;
    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:NP160172.RAU4NM98yd1mjz6FmDsawOj9iwRaEXn5FH_fw-i19CWrM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:26+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" .
}