@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP871231.RAKNAb4TWtMwqGEwidIgfXhqaVXvzpKrqtdJ96ReYDgrQ> .
@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:NP871231.RAKNAb4TWtMwqGEwidIgfXhqaVXvzpKrqtdJ96ReYDgrQ130_head {
  this: np:hasAssertion dgn-np:NP871231.RAKNAb4TWtMwqGEwidIgfXhqaVXvzpKrqtdJ96ReYDgrQ130_assertion;
    np:hasProvenance dgn-np:NP871231.RAKNAb4TWtMwqGEwidIgfXhqaVXvzpKrqtdJ96ReYDgrQ130_provenance;
    np:hasPublicationInfo dgn-np:NP871231.RAKNAb4TWtMwqGEwidIgfXhqaVXvzpKrqtdJ96ReYDgrQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP871231.RAKNAb4TWtMwqGEwidIgfXhqaVXvzpKrqtdJ96ReYDgrQ130_assertion a np:Assertion .
  
  dgn-np:NP871231.RAKNAb4TWtMwqGEwidIgfXhqaVXvzpKrqtdJ96ReYDgrQ130_provenance a np:Provenance .
  
  dgn-np:NP871231.RAKNAb4TWtMwqGEwidIgfXhqaVXvzpKrqtdJ96ReYDgrQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP871231.RAKNAb4TWtMwqGEwidIgfXhqaVXvzpKrqtdJ96ReYDgrQ130_assertion {
  miriam-gene:54741 a ncit:C16612 .
  
  lld:C0028754 a ncit:C7057 .
  
  dgn-gda:DGN5350cdba4a12529a5d2d83be7cd5698a sio:SIO_000628 miriam-gene:54741, lld:C0028754;
    a sio:SIO_001121 .
}

dgn-np:NP871231.RAKNAb4TWtMwqGEwidIgfXhqaVXvzpKrqtdJ96ReYDgrQ130_provenance {
  dgn-np:NP871231.RAKNAb4TWtMwqGEwidIgfXhqaVXvzpKrqtdJ96ReYDgrQ130_assertion dcterms:description
      "[In conclusion, finding this new mutation in the LEPR beside our previous mutation in the LEP gene implies that monogenic obesity syndromes may be common in the Egyptian population owing to the high rates of consanguineous marriages.]. 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:21306929;
    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:NP871231.RAKNAb4TWtMwqGEwidIgfXhqaVXvzpKrqtdJ96ReYDgrQ130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:19+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" .
}