@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP43852.RAtjqxgh9c10y_xIcX5AC60wGPWmtCLU91zEug6h92b7Y> .
@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 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:NP43852.RAtjqxgh9c10y_xIcX5AC60wGPWmtCLU91zEug6h92b7Y130_head {
  this: np:hasAssertion dgn-np:NP43852.RAtjqxgh9c10y_xIcX5AC60wGPWmtCLU91zEug6h92b7Y130_assertion;
    np:hasProvenance dgn-np:NP43852.RAtjqxgh9c10y_xIcX5AC60wGPWmtCLU91zEug6h92b7Y130_provenance;
    np:hasPublicationInfo dgn-np:NP43852.RAtjqxgh9c10y_xIcX5AC60wGPWmtCLU91zEug6h92b7Y130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP43852.RAtjqxgh9c10y_xIcX5AC60wGPWmtCLU91zEug6h92b7Y130_assertion a np:Assertion .
  
  dgn-np:NP43852.RAtjqxgh9c10y_xIcX5AC60wGPWmtCLU91zEug6h92b7Y130_provenance a np:Provenance .
  
  dgn-np:NP43852.RAtjqxgh9c10y_xIcX5AC60wGPWmtCLU91zEug6h92b7Y130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP43852.RAtjqxgh9c10y_xIcX5AC60wGPWmtCLU91zEug6h92b7Y130_assertion {
  miriam-gene:2525 a ncit:C16612 .
  
  lld:C0028754 a ncit:C7057 .
  
  dgn-gda:DGN7bb2c5f5c5c251f913b994f543d761f2 sio:SIO_000628 miriam-gene:2525, lld:C0028754;
    a sio:SIO_001122 .
}

dgn-np:NP43852.RAtjqxgh9c10y_xIcX5AC60wGPWmtCLU91zEug6h92b7Y130_provenance {
  dgn-np:NP43852.RAtjqxgh9c10y_xIcX5AC60wGPWmtCLU91zEug6h92b7Y130_assertion dct:description
      "[The frequency of the Le(a-b-) phenotype may vary substantially in different populations. Identification of this new genetic marker of obesity may, for example, contribute to the explanation of individual and ethnic differences in the prevalence of 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:15832169;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP43852.RAtjqxgh9c10y_xIcX5AC60wGPWmtCLU91zEug6h92b7Y130_publicationInfo {
  this: dct:created "2014-10-02T12:32:20+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}