@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP447117.RAOiRvstyL2gZWkv393n3Jw-4JPU9cqqL76UylcyhtMfI> .
@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:NP447117.RAOiRvstyL2gZWkv393n3Jw-4JPU9cqqL76UylcyhtMfI130_head {
  this: np:hasAssertion dgn-np:NP447117.RAOiRvstyL2gZWkv393n3Jw-4JPU9cqqL76UylcyhtMfI130_assertion;
    np:hasProvenance dgn-np:NP447117.RAOiRvstyL2gZWkv393n3Jw-4JPU9cqqL76UylcyhtMfI130_provenance;
    np:hasPublicationInfo dgn-np:NP447117.RAOiRvstyL2gZWkv393n3Jw-4JPU9cqqL76UylcyhtMfI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP447117.RAOiRvstyL2gZWkv393n3Jw-4JPU9cqqL76UylcyhtMfI130_assertion a np:Assertion .
  
  dgn-np:NP447117.RAOiRvstyL2gZWkv393n3Jw-4JPU9cqqL76UylcyhtMfI130_provenance a np:Provenance .
  
  dgn-np:NP447117.RAOiRvstyL2gZWkv393n3Jw-4JPU9cqqL76UylcyhtMfI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP447117.RAOiRvstyL2gZWkv393n3Jw-4JPU9cqqL76UylcyhtMfI130_assertion {
  miriam-gene:3126 a ncit:C16612 .
  
  lld:C0018995 a ncit:C7057 .
  
  dgn-gda:DGN98b2d72548e2102c3dfbc26a089d3125 sio:SIO_000628 miriam-gene:3126, lld:C0018995;
    a sio:SIO_001121 .
}

dgn-np:NP447117.RAOiRvstyL2gZWkv393n3Jw-4JPU9cqqL76UylcyhtMfI130_provenance {
  dgn-np:NP447117.RAOiRvstyL2gZWkv393n3Jw-4JPU9cqqL76UylcyhtMfI130_assertion dcterms:description
      "[We performed univariate and multivariate analyses of the relationships of human leukocyte antigen (HLA)-A*03 and HLA haplotype A*03-B*07 to iron measures (serum iron concentration, transferrin saturation, and serum ferritin concentration at diagnosis and units of phlebotomy to achieve iron depletion) in hemochromatosis probands homozygous for HFE C282Y diagnosed in medical care.]. 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:15607698;
    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:NP447117.RAOiRvstyL2gZWkv393n3Jw-4JPU9cqqL76UylcyhtMfI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:26+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" .
}