@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP210978.RAdc_TeOm5AoEiftZiBQe-WKD4z1Vu7UTKnF1QjEcYSAA> .
@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:NP210978.RAdc_TeOm5AoEiftZiBQe-WKD4z1Vu7UTKnF1QjEcYSAA130_head {
  this: np:hasAssertion dgn-np:NP210978.RAdc_TeOm5AoEiftZiBQe-WKD4z1Vu7UTKnF1QjEcYSAA130_assertion;
    np:hasProvenance dgn-np:NP210978.RAdc_TeOm5AoEiftZiBQe-WKD4z1Vu7UTKnF1QjEcYSAA130_provenance;
    np:hasPublicationInfo dgn-np:NP210978.RAdc_TeOm5AoEiftZiBQe-WKD4z1Vu7UTKnF1QjEcYSAA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP210978.RAdc_TeOm5AoEiftZiBQe-WKD4z1Vu7UTKnF1QjEcYSAA130_assertion a np:Assertion .
  
  dgn-np:NP210978.RAdc_TeOm5AoEiftZiBQe-WKD4z1Vu7UTKnF1QjEcYSAA130_provenance a np:Provenance .
  
  dgn-np:NP210978.RAdc_TeOm5AoEiftZiBQe-WKD4z1Vu7UTKnF1QjEcYSAA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP210978.RAdc_TeOm5AoEiftZiBQe-WKD4z1Vu7UTKnF1QjEcYSAA130_assertion {
  miriam-gene:57817 a ncit:C16612 .
  
  lld:C0002871 a ncit:C7057 .
  
  dgn-gda:DGN03343245a27441dcabc9d66c753203b7 sio:SIO_000628 miriam-gene:57817, lld:C0002871;
    a sio:SIO_001121 .
}

dgn-np:NP210978.RAdc_TeOm5AoEiftZiBQe-WKD4z1Vu7UTKnF1QjEcYSAA130_provenance {
  dgn-np:NP210978.RAdc_TeOm5AoEiftZiBQe-WKD4z1Vu7UTKnF1QjEcYSAA130_assertion dcterms:description
      "[Evaluation of the effect of TMPRSS6 genotype on clinical outcomes in prospective studies in CHD may be useful to predict the outcomes of hepcidin manipulation, and to guide treatment personalization by optimizing anemia management.]. 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:23433094;
    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:NP210978.RAdc_TeOm5AoEiftZiBQe-WKD4z1Vu7UTKnF1QjEcYSAA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:56+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" .
}