@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP466318.RAccydsOWbrvLHnlyui55Ph__N8GzAeImpYF2nNTeTXcU> .
@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:NP466318.RAccydsOWbrvLHnlyui55Ph__N8GzAeImpYF2nNTeTXcU130_head {
  this: np:hasAssertion dgn-np:NP466318.RAccydsOWbrvLHnlyui55Ph__N8GzAeImpYF2nNTeTXcU130_assertion;
    np:hasProvenance dgn-np:NP466318.RAccydsOWbrvLHnlyui55Ph__N8GzAeImpYF2nNTeTXcU130_provenance;
    np:hasPublicationInfo dgn-np:NP466318.RAccydsOWbrvLHnlyui55Ph__N8GzAeImpYF2nNTeTXcU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP466318.RAccydsOWbrvLHnlyui55Ph__N8GzAeImpYF2nNTeTXcU130_assertion a np:Assertion .
  
  dgn-np:NP466318.RAccydsOWbrvLHnlyui55Ph__N8GzAeImpYF2nNTeTXcU130_provenance a np:Provenance .
  
  dgn-np:NP466318.RAccydsOWbrvLHnlyui55Ph__N8GzAeImpYF2nNTeTXcU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP466318.RAccydsOWbrvLHnlyui55Ph__N8GzAeImpYF2nNTeTXcU130_assertion {
  miriam-gene:3077 a ncit:C16612 .
  
  lld:C0240066 a ncit:C7057 .
  
  dgn-gda:DGNe8bec1bde9d45f6ab635c4f07c44408f sio:SIO_000628 miriam-gene:3077, lld:C0240066;
    a sio:SIO_001121 .
}

dgn-np:NP466318.RAccydsOWbrvLHnlyui55Ph__N8GzAeImpYF2nNTeTXcU130_provenance {
  dgn-np:NP466318.RAccydsOWbrvLHnlyui55Ph__N8GzAeImpYF2nNTeTXcU130_assertion dcterms:description
      "[HFE deficiency in intestinal crypt cells is thought to cause intestinal iron deficiency and greater expression of iron transporters such as SLC11A2 (also called DMT1, DCT1 and NRAMP2) and SLC11A3 (also called IREG1, ferroportin and MTP1; ref.]. 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:12704390;
    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:NP466318.RAccydsOWbrvLHnlyui55Ph__N8GzAeImpYF2nNTeTXcU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:40+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" .
}