@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP975167.RAJo36j7MfROMBgufQ4VTWCePGbE6i6aspRaSUeGLHils> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .
dgn-np:NP975167.RAJo36j7MfROMBgufQ4VTWCePGbE6i6aspRaSUeGLHils130_head {
  this: np:hasAssertion dgn-np:NP975167.RAJo36j7MfROMBgufQ4VTWCePGbE6i6aspRaSUeGLHils130_assertion ;
    np:hasProvenance dgn-np:NP975167.RAJo36j7MfROMBgufQ4VTWCePGbE6i6aspRaSUeGLHils130_provenance ;
    np:hasPublicationInfo dgn-np:NP975167.RAJo36j7MfROMBgufQ4VTWCePGbE6i6aspRaSUeGLHils130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP975167.RAJo36j7MfROMBgufQ4VTWCePGbE6i6aspRaSUeGLHils130_assertion a np:Assertion .
  dgn-np:NP975167.RAJo36j7MfROMBgufQ4VTWCePGbE6i6aspRaSUeGLHils130_provenance a np:Provenance .
  dgn-np:NP975167.RAJo36j7MfROMBgufQ4VTWCePGbE6i6aspRaSUeGLHils130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP975167.RAJo36j7MfROMBgufQ4VTWCePGbE6i6aspRaSUeGLHils130_assertion {
  miriam-gene:148738 a ncit:C16612 .
  lld:C0392514 a ncit:C7057 .
  dgn-gda:DGNe65b38bec57fd09d6b4aa62dbad54065 sio:SIO_000628 miriam-gene:148738 , lld:C0392514 ;
    a sio:SIO_001121 .
}
dgn-np:NP975167.RAJo36j7MfROMBgufQ4VTWCePGbE6i6aspRaSUeGLHils130_provenance {
  dgn-np:NP975167.RAJo36j7MfROMBgufQ4VTWCePGbE6i6aspRaSUeGLHils130_assertion dcterms:description "[Type 2A HH is caused by mutations in the recently cloned hemojuvelin gene (HJV; also called HFE2) (Papanikolaou, G., Samuels, M. E., Ludwig, E. H., MacDonald, M. L., Franchini, P. L., Dube, M. P., Andres, L., MacFarlane, J., Sakellaropoulos, N., Politou, M., Nemeth, E., Thompson, J., Risler, J. K., Zaborowska, C., Babakaiff, R., Radomski, C. C., Pape, T. D., Davidas, O., Christakis, J., Brissot, P., Lockitch, G., Ganz, T., Hayden, M. R., and Goldberg, Y. P. (2004) Nat.]. 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:16103117 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP975167.RAJo36j7MfROMBgufQ4VTWCePGbE6i6aspRaSUeGLHils130_publicationInfo {
  this: dcterms:created "2015-08-25T14:47:35+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:disgenetv3.0rdf ;
    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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}