@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP67368.RAiT6ROgBPNo7FlOrBfHGeuQQryADDISyZzmVGjAyaQUk> .
@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:NP67368.RAiT6ROgBPNo7FlOrBfHGeuQQryADDISyZzmVGjAyaQUk130_head {
  this: np:hasAssertion dgn-np:NP67368.RAiT6ROgBPNo7FlOrBfHGeuQQryADDISyZzmVGjAyaQUk130_assertion;
    np:hasProvenance dgn-np:NP67368.RAiT6ROgBPNo7FlOrBfHGeuQQryADDISyZzmVGjAyaQUk130_provenance;
    np:hasPublicationInfo dgn-np:NP67368.RAiT6ROgBPNo7FlOrBfHGeuQQryADDISyZzmVGjAyaQUk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP67368.RAiT6ROgBPNo7FlOrBfHGeuQQryADDISyZzmVGjAyaQUk130_assertion a np:Assertion .
  
  dgn-np:NP67368.RAiT6ROgBPNo7FlOrBfHGeuQQryADDISyZzmVGjAyaQUk130_provenance a np:Provenance .
  
  dgn-np:NP67368.RAiT6ROgBPNo7FlOrBfHGeuQQryADDISyZzmVGjAyaQUk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP67368.RAiT6ROgBPNo7FlOrBfHGeuQQryADDISyZzmVGjAyaQUk130_assertion {
  miriam-gene:3077 a ncit:C16612 .
  
  lld:C0282193 a ncit:C7057 .
  
  dgn-gda:DGN0422c04030f34c6ecb1975cd056c1015 sio:SIO_000628 miriam-gene:3077, lld:C0282193;
    a sio:SIO_001122 .
}

dgn-np:NP67368.RAiT6ROgBPNo7FlOrBfHGeuQQryADDISyZzmVGjAyaQUk130_provenance {
  dgn-np:NP67368.RAiT6ROgBPNo7FlOrBfHGeuQQryADDISyZzmVGjAyaQUk130_assertion dcterms:description
      "[The simultaneous detection of 18 known HFE, TFR2 and FPN1 mutations and sequencing of the HAMP gene were performed to rule out the possible existence of genetic modifier factors related with iron overload.]. 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:17042772;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP67368.RAiT6ROgBPNo7FlOrBfHGeuQQryADDISyZzmVGjAyaQUk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:32+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" .
}