@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP741464.RAJZ_zalNgINBF8_9zjF4uUIwllpjLZeDznmkNjwwypd0> .
@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:NP741464.RAJZ_zalNgINBF8_9zjF4uUIwllpjLZeDznmkNjwwypd0130_head {
  this: np:hasAssertion dgn-np:NP741464.RAJZ_zalNgINBF8_9zjF4uUIwllpjLZeDznmkNjwwypd0130_assertion ;
    np:hasProvenance dgn-np:NP741464.RAJZ_zalNgINBF8_9zjF4uUIwllpjLZeDznmkNjwwypd0130_provenance ;
    np:hasPublicationInfo dgn-np:NP741464.RAJZ_zalNgINBF8_9zjF4uUIwllpjLZeDznmkNjwwypd0130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP741464.RAJZ_zalNgINBF8_9zjF4uUIwllpjLZeDznmkNjwwypd0130_assertion a np:Assertion .
  dgn-np:NP741464.RAJZ_zalNgINBF8_9zjF4uUIwllpjLZeDznmkNjwwypd0130_provenance a np:Provenance .
  dgn-np:NP741464.RAJZ_zalNgINBF8_9zjF4uUIwllpjLZeDznmkNjwwypd0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP741464.RAJZ_zalNgINBF8_9zjF4uUIwllpjLZeDznmkNjwwypd0130_assertion {
  miriam-gene:3077 a ncit:C16612 .
  lld:C0020538 a ncit:C7057 .
  dgn-gda:DGN547343f88f0f66dc7129687f77cab962 sio:SIO_000628 miriam-gene:3077 , lld:C0020538 ;
    a sio:SIO_001121 .
}
dgn-np:NP741464.RAJZ_zalNgINBF8_9zjF4uUIwllpjLZeDznmkNjwwypd0130_provenance {
  dgn-np:NP741464.RAJZ_zalNgINBF8_9zjF4uUIwllpjLZeDznmkNjwwypd0130_assertion dcterms:description "[A total of 87 persons with hemochromatosis (patients) (39 women, 48 men), who underwent HFE genotyping, and 50 persons with hypertension (controls) (22 women, 28 men), who had not undergone HFE genotyping, completed a structured interview in which they reported attitudes about benefits and disadvantages of genetic testing and their understanding of genetics and hemochromatosis.]. 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:15345103 ;
    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:NP741464.RAJZ_zalNgINBF8_9zjF4uUIwllpjLZeDznmkNjwwypd0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:30+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" .
}