@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP683143.RAl36fsD6mkMM1IHCg_X-f1gYaWt9PvnYZiHI6GKKipcg> .
@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:NP683143.RAl36fsD6mkMM1IHCg_X-f1gYaWt9PvnYZiHI6GKKipcg130_head {
  this: np:hasAssertion dgn-np:NP683143.RAl36fsD6mkMM1IHCg_X-f1gYaWt9PvnYZiHI6GKKipcg130_assertion;
    np:hasProvenance dgn-np:NP683143.RAl36fsD6mkMM1IHCg_X-f1gYaWt9PvnYZiHI6GKKipcg130_provenance;
    np:hasPublicationInfo dgn-np:NP683143.RAl36fsD6mkMM1IHCg_X-f1gYaWt9PvnYZiHI6GKKipcg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP683143.RAl36fsD6mkMM1IHCg_X-f1gYaWt9PvnYZiHI6GKKipcg130_assertion a np:Assertion .
  
  dgn-np:NP683143.RAl36fsD6mkMM1IHCg_X-f1gYaWt9PvnYZiHI6GKKipcg130_provenance a np:Provenance .
  
  dgn-np:NP683143.RAl36fsD6mkMM1IHCg_X-f1gYaWt9PvnYZiHI6GKKipcg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP683143.RAl36fsD6mkMM1IHCg_X-f1gYaWt9PvnYZiHI6GKKipcg130_assertion {
  miriam-gene:3240 a ncit:C16612 .
  
  lld:C0023343 a ncit:C7057 .
  
  dgn-gda:DGN95400644ce71f981daacf6ed157eb843 sio:SIO_000628 miriam-gene:3240, lld:C0023343;
    a sio:SIO_001121 .
}

dgn-np:NP683143.RAl36fsD6mkMM1IHCg_X-f1gYaWt9PvnYZiHI6GKKipcg130_provenance {
  dgn-np:NP683143.RAl36fsD6mkMM1IHCg_X-f1gYaWt9PvnYZiHI6GKKipcg130_assertion dcterms:description
      "[Thus, although this genetic marker did not correlate with the occurrence of the variety of disease, it is possible that leprosy caused inhibition of haptoglobin synthesis and therefore an apparent increased frequency of the 0-0 phenotype.]. 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:7193656;
    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:NP683143.RAl36fsD6mkMM1IHCg_X-f1gYaWt9PvnYZiHI6GKKipcg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:55+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" .
}