@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP150831.RA2xz0PHHNQxso0EZAe7FM_sDEeM3JYG2leNJk6tiv018> .
@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:NP150831.RA2xz0PHHNQxso0EZAe7FM_sDEeM3JYG2leNJk6tiv018130_head {
  this: np:hasAssertion dgn-np:NP150831.RA2xz0PHHNQxso0EZAe7FM_sDEeM3JYG2leNJk6tiv018130_assertion;
    np:hasProvenance dgn-np:NP150831.RA2xz0PHHNQxso0EZAe7FM_sDEeM3JYG2leNJk6tiv018130_provenance;
    np:hasPublicationInfo dgn-np:NP150831.RA2xz0PHHNQxso0EZAe7FM_sDEeM3JYG2leNJk6tiv018130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP150831.RA2xz0PHHNQxso0EZAe7FM_sDEeM3JYG2leNJk6tiv018130_assertion a np:Assertion .
  
  dgn-np:NP150831.RA2xz0PHHNQxso0EZAe7FM_sDEeM3JYG2leNJk6tiv018130_provenance a np:Provenance .
  
  dgn-np:NP150831.RA2xz0PHHNQxso0EZAe7FM_sDEeM3JYG2leNJk6tiv018130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP150831.RA2xz0PHHNQxso0EZAe7FM_sDEeM3JYG2leNJk6tiv018130_assertion {
  miriam-gene:3077 a ncit:C16612 .
  
  lld:C0282193 a ncit:C7057 .
  
  dgn-gda:DGN2c0ff57df8b10d02bad8a993ef597be0 sio:SIO_000628 miriam-gene:3077, lld:C0282193;
    a sio:SIO_001122 .
}

dgn-np:NP150831.RA2xz0PHHNQxso0EZAe7FM_sDEeM3JYG2leNJk6tiv018130_provenance {
  dgn-np:NP150831.RA2xz0PHHNQxso0EZAe7FM_sDEeM3JYG2leNJk6tiv018130_assertion dcterms:description
      "[study of H63D homozygotes supports the conclusion that this genotype must be taken into account, because it confers an increased risk of iron overload and genetic susceptibility to developing hereditary hemochromatosis or to aggravating other diseases ]. 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:16364490;
    prov:wasDerivedFrom dgn-void:lhgdn-20090331;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:lhgdn-20090331 pav:importedOn "2009-03-31"^^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:NP150831.RA2xz0PHHNQxso0EZAe7FM_sDEeM3JYG2leNJk6tiv018130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:20+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" .
}