@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP50158.RACSxm9WIlC3oUPIwM7YpmvalQ9TcYiVTtlwmHzHj3SFQ> .
@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/v3.0.0/void/> .

dgn-np:NP50158.RACSxm9WIlC3oUPIwM7YpmvalQ9TcYiVTtlwmHzHj3SFQ130_head {
  this: np:hasAssertion dgn-np:NP50158.RACSxm9WIlC3oUPIwM7YpmvalQ9TcYiVTtlwmHzHj3SFQ130_assertion;
    np:hasProvenance dgn-np:NP50158.RACSxm9WIlC3oUPIwM7YpmvalQ9TcYiVTtlwmHzHj3SFQ130_provenance;
    np:hasPublicationInfo dgn-np:NP50158.RACSxm9WIlC3oUPIwM7YpmvalQ9TcYiVTtlwmHzHj3SFQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP50158.RACSxm9WIlC3oUPIwM7YpmvalQ9TcYiVTtlwmHzHj3SFQ130_assertion a np:Assertion .
  
  dgn-np:NP50158.RACSxm9WIlC3oUPIwM7YpmvalQ9TcYiVTtlwmHzHj3SFQ130_provenance a np:Provenance .
  
  dgn-np:NP50158.RACSxm9WIlC3oUPIwM7YpmvalQ9TcYiVTtlwmHzHj3SFQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP50158.RACSxm9WIlC3oUPIwM7YpmvalQ9TcYiVTtlwmHzHj3SFQ130_assertion {
  miriam-gene:3077 a ncit:C16612 .
  
  lld:C0011860 a ncit:C7057 .
  
  dgn-gda:DGN3d82d7449e13df57a93b1260f5c02cc9 sio:SIO_000628 miriam-gene:3077, lld:C0011860;
    a sio:SIO_001122 .
}

dgn-np:NP50158.RACSxm9WIlC3oUPIwM7YpmvalQ9TcYiVTtlwmHzHj3SFQ130_provenance {
  dgn-np:NP50158.RACSxm9WIlC3oUPIwM7YpmvalQ9TcYiVTtlwmHzHj3SFQ130_assertion dcterms:description
      "[ HJV I222N and G320V are probably uncommon causes or modifiers of primary iron overload in adult whites and African Americans in Alabama. Double heterozygosity for HJV I222N and HFE C282Y may not promote increased iron absorption.]. 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:15610558;
    prov:wasDerivedFrom dgn-void:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP50158.RACSxm9WIlC3oUPIwM7YpmvalQ9TcYiVTtlwmHzHj3SFQ130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:07+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}