@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP160925.RAbEdMsXFq71YvsKxFiOFHF3tkXGP-4NuW_pug6pZfass> .
@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:NP160925.RAbEdMsXFq71YvsKxFiOFHF3tkXGP-4NuW_pug6pZfass130_head {
  this: np:hasAssertion dgn-np:NP160925.RAbEdMsXFq71YvsKxFiOFHF3tkXGP-4NuW_pug6pZfass130_assertion;
    np:hasProvenance dgn-np:NP160925.RAbEdMsXFq71YvsKxFiOFHF3tkXGP-4NuW_pug6pZfass130_provenance;
    np:hasPublicationInfo dgn-np:NP160925.RAbEdMsXFq71YvsKxFiOFHF3tkXGP-4NuW_pug6pZfass130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP160925.RAbEdMsXFq71YvsKxFiOFHF3tkXGP-4NuW_pug6pZfass130_assertion a np:Assertion .
  
  dgn-np:NP160925.RAbEdMsXFq71YvsKxFiOFHF3tkXGP-4NuW_pug6pZfass130_provenance a np:Provenance .
  
  dgn-np:NP160925.RAbEdMsXFq71YvsKxFiOFHF3tkXGP-4NuW_pug6pZfass130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP160925.RAbEdMsXFq71YvsKxFiOFHF3tkXGP-4NuW_pug6pZfass130_assertion {
  miriam-gene:3077 a ncit:C16612 .
  
  lld:C0282193 a ncit:C7057 .
  
  dgn-gda:DGN57e3030c372331a1d2cb419f97fde7c2 sio:SIO_000628 miriam-gene:3077, lld:C0282193;
    a sio:SIO_001121 .
}

dgn-np:NP160925.RAbEdMsXFq71YvsKxFiOFHF3tkXGP-4NuW_pug6pZfass130_provenance {
  dgn-np:NP160925.RAbEdMsXFq71YvsKxFiOFHF3tkXGP-4NuW_pug6pZfass130_assertion dcterms:description
      "[To describe the clinical expression of iron overload (IO) associated with H63D homozygosity, and search for potential genetic modifiers (within the HFE or other genes) that could explain the variability of the phenotypes.]. 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:11358905;
    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:NP160925.RAbEdMsXFq71YvsKxFiOFHF3tkXGP-4NuW_pug6pZfass130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:27+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" .
}