@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP861349.RA32BGvPRoYVM2sBojXw9L1lE8q4ehTYokk5rriFBVzGA> .
@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:NP861349.RA32BGvPRoYVM2sBojXw9L1lE8q4ehTYokk5rriFBVzGA130_head {
  this: np:hasAssertion dgn-np:NP861349.RA32BGvPRoYVM2sBojXw9L1lE8q4ehTYokk5rriFBVzGA130_assertion;
    np:hasProvenance dgn-np:NP861349.RA32BGvPRoYVM2sBojXw9L1lE8q4ehTYokk5rriFBVzGA130_provenance;
    np:hasPublicationInfo dgn-np:NP861349.RA32BGvPRoYVM2sBojXw9L1lE8q4ehTYokk5rriFBVzGA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP861349.RA32BGvPRoYVM2sBojXw9L1lE8q4ehTYokk5rriFBVzGA130_assertion a np:Assertion .
  
  dgn-np:NP861349.RA32BGvPRoYVM2sBojXw9L1lE8q4ehTYokk5rriFBVzGA130_provenance a np:Provenance .
  
  dgn-np:NP861349.RA32BGvPRoYVM2sBojXw9L1lE8q4ehTYokk5rriFBVzGA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP861349.RA32BGvPRoYVM2sBojXw9L1lE8q4ehTYokk5rriFBVzGA130_assertion {
  miriam-gene:2235 a ncit:C16612 .
  
  lld:C1275125 a ncit:C7057 .
  
  dgn-gda:DGN8ebcc15ec981384429f0a50972f1e363 sio:SIO_000628 miriam-gene:2235, lld:C1275125;
    a sio:SIO_001121 .
}

dgn-np:NP861349.RA32BGvPRoYVM2sBojXw9L1lE8q4ehTYokk5rriFBVzGA130_provenance {
  dgn-np:NP861349.RA32BGvPRoYVM2sBojXw9L1lE8q4ehTYokk5rriFBVzGA130_assertion dcterms:description
      "[Erythropoietic protoporphyria (EPP) is an inherited disorder of porphyrin metabolism in which decreased activity of ferrochelatase (FECH) leads to accumulation of protoporphyrin IX (PP IX) in red blood cells, plasma, liver, and bile, and increased PP IX excretion in feces.]. 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:19693296;
    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:NP861349.RA32BGvPRoYVM2sBojXw9L1lE8q4ehTYokk5rriFBVzGA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:46+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" .
}