@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP57570.RALUB-8f8Cfp14jLJQkGVWSSUgkksYigZ4SBEfKhlvFi0> .
@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:NP57570.RALUB-8f8Cfp14jLJQkGVWSSUgkksYigZ4SBEfKhlvFi0130_head {
  this: np:hasAssertion dgn-np:NP57570.RALUB-8f8Cfp14jLJQkGVWSSUgkksYigZ4SBEfKhlvFi0130_assertion;
    np:hasProvenance dgn-np:NP57570.RALUB-8f8Cfp14jLJQkGVWSSUgkksYigZ4SBEfKhlvFi0130_provenance;
    np:hasPublicationInfo dgn-np:NP57570.RALUB-8f8Cfp14jLJQkGVWSSUgkksYigZ4SBEfKhlvFi0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP57570.RALUB-8f8Cfp14jLJQkGVWSSUgkksYigZ4SBEfKhlvFi0130_assertion a np:Assertion .
  
  dgn-np:NP57570.RALUB-8f8Cfp14jLJQkGVWSSUgkksYigZ4SBEfKhlvFi0130_provenance a np:Provenance .
  
  dgn-np:NP57570.RALUB-8f8Cfp14jLJQkGVWSSUgkksYigZ4SBEfKhlvFi0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP57570.RALUB-8f8Cfp14jLJQkGVWSSUgkksYigZ4SBEfKhlvFi0130_assertion {
  miriam-gene:3240 a ncit:C16612 .
  
  lld:C0024535 a ncit:C7057 .
  
  dgn-gda:DGNe96a44fd906fc1aee93c44022bb26aff sio:SIO_000628 miriam-gene:3240, lld:C0024535;
    a sio:SIO_001122 .
}

dgn-np:NP57570.RALUB-8f8Cfp14jLJQkGVWSSUgkksYigZ4SBEfKhlvFi0130_provenance {
  dgn-np:NP57570.RALUB-8f8Cfp14jLJQkGVWSSUgkksYigZ4SBEfKhlvFi0130_assertion dcterms:description
      "[ We propose that previous conflicting results between Hp phenotypes/genotypes and malaria susceptibility may be explained by differing prevalence of the A-61C SNP in the populations studied, which we found to be highly associated with the Hp2 allele. We report the -61C allele to be associated with decreased Hp protein levels (independent of Hp phenotype), confirming in vitro studies. Decreased Hp expression may lead to increased oxidant stress and increased red cell turnover, and facilitate the development of acquired immunity, similar to a mechanism suggested for sickle cell trait.]. 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:17426810;
    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:NP57570.RALUB-8f8Cfp14jLJQkGVWSSUgkksYigZ4SBEfKhlvFi0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:27+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" .
}