@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP604638.RAVqi79jl1gG8NXZ_o_QXRA-UWh7Yk0v6JOPcpF8avHXM> .
@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:NP604638.RAVqi79jl1gG8NXZ_o_QXRA-UWh7Yk0v6JOPcpF8avHXM130_head {
  this: np:hasAssertion dgn-np:NP604638.RAVqi79jl1gG8NXZ_o_QXRA-UWh7Yk0v6JOPcpF8avHXM130_assertion;
    np:hasProvenance dgn-np:NP604638.RAVqi79jl1gG8NXZ_o_QXRA-UWh7Yk0v6JOPcpF8avHXM130_provenance;
    np:hasPublicationInfo dgn-np:NP604638.RAVqi79jl1gG8NXZ_o_QXRA-UWh7Yk0v6JOPcpF8avHXM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP604638.RAVqi79jl1gG8NXZ_o_QXRA-UWh7Yk0v6JOPcpF8avHXM130_assertion a np:Assertion .
  
  dgn-np:NP604638.RAVqi79jl1gG8NXZ_o_QXRA-UWh7Yk0v6JOPcpF8avHXM130_provenance a np:Provenance .
  
  dgn-np:NP604638.RAVqi79jl1gG8NXZ_o_QXRA-UWh7Yk0v6JOPcpF8avHXM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP604638.RAVqi79jl1gG8NXZ_o_QXRA-UWh7Yk0v6JOPcpF8avHXM130_assertion {
  miriam-gene:3077 a ncit:C16612 .
  
  lld:C0011847 a ncit:C7057 .
  
  dgn-gda:DGNb06f4f37d31b0f8d23f3d3c480416a4a sio:SIO_000628 miriam-gene:3077, lld:C0011847;
    a sio:SIO_001121 .
}

dgn-np:NP604638.RAVqi79jl1gG8NXZ_o_QXRA-UWh7Yk0v6JOPcpF8avHXM130_provenance {
  dgn-np:NP604638.RAVqi79jl1gG8NXZ_o_QXRA-UWh7Yk0v6JOPcpF8avHXM130_assertion dcterms:description
      "[Hereditary Hemochromatosis (HH) is an iron overload syndrome caused by increased duodenal iron absorption, which leads to excessive iron deposition in parenchymal cells of the liver and mayor organs, causing cirrhosis, diabetes, cardiac failure, endocrine complications and arthritis.]. 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:19656448;
    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:NP604638.RAVqi79jl1gG8NXZ_o_QXRA-UWh7Yk0v6JOPcpF8avHXM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:03+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" .
}