@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP167140.RAqzziw-mfyBAiEvNVaPijILSkIE1d7zr-QZSPIRaHsEQ> .
@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:NP167140.RAqzziw-mfyBAiEvNVaPijILSkIE1d7zr-QZSPIRaHsEQ130_head {
  this: np:hasAssertion dgn-np:NP167140.RAqzziw-mfyBAiEvNVaPijILSkIE1d7zr-QZSPIRaHsEQ130_assertion;
    np:hasProvenance dgn-np:NP167140.RAqzziw-mfyBAiEvNVaPijILSkIE1d7zr-QZSPIRaHsEQ130_provenance;
    np:hasPublicationInfo dgn-np:NP167140.RAqzziw-mfyBAiEvNVaPijILSkIE1d7zr-QZSPIRaHsEQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP167140.RAqzziw-mfyBAiEvNVaPijILSkIE1d7zr-QZSPIRaHsEQ130_assertion a np:Assertion .
  
  dgn-np:NP167140.RAqzziw-mfyBAiEvNVaPijILSkIE1d7zr-QZSPIRaHsEQ130_provenance a np:Provenance .
  
  dgn-np:NP167140.RAqzziw-mfyBAiEvNVaPijILSkIE1d7zr-QZSPIRaHsEQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP167140.RAqzziw-mfyBAiEvNVaPijILSkIE1d7zr-QZSPIRaHsEQ130_assertion {
  miriam-gene:3077 a ncit:C16612 .
  
  lld:C0282193 a ncit:C7057 .
  
  dgn-gda:DGN3a925ef7c699cf7ff7a83b1b6bdcff3c sio:SIO_000628 miriam-gene:3077, lld:C0282193;
    a sio:SIO_001122 .
}

dgn-np:NP167140.RAqzziw-mfyBAiEvNVaPijILSkIE1d7zr-QZSPIRaHsEQ130_provenance {
  dgn-np:NP167140.RAqzziw-mfyBAiEvNVaPijILSkIE1d7zr-QZSPIRaHsEQ130_assertion dcterms:description
      "[The presence of H63D mutations was an independent factor associated with NAFLD and elevated TS. Therefore, the H63D mutation may increase susceptibility to NAFLD probably associated with peripheral iron overload, especially in males.]. 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:20216079;
    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:NP167140.RAqzziw-mfyBAiEvNVaPijILSkIE1d7zr-QZSPIRaHsEQ130_publicationInfo {
  this: dcterms:created "2016-05-13T12:43:03+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" .
}