@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP901564.RA62PfNrMMnmLIzV7HAVpc3YkfOyfmZ8j3BBfMgdgFYvM> .
@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:NP901564.RA62PfNrMMnmLIzV7HAVpc3YkfOyfmZ8j3BBfMgdgFYvM130_head {
  this: np:hasAssertion dgn-np:NP901564.RA62PfNrMMnmLIzV7HAVpc3YkfOyfmZ8j3BBfMgdgFYvM130_assertion;
    np:hasProvenance dgn-np:NP901564.RA62PfNrMMnmLIzV7HAVpc3YkfOyfmZ8j3BBfMgdgFYvM130_provenance;
    np:hasPublicationInfo dgn-np:NP901564.RA62PfNrMMnmLIzV7HAVpc3YkfOyfmZ8j3BBfMgdgFYvM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP901564.RA62PfNrMMnmLIzV7HAVpc3YkfOyfmZ8j3BBfMgdgFYvM130_assertion a np:Assertion .
  
  dgn-np:NP901564.RA62PfNrMMnmLIzV7HAVpc3YkfOyfmZ8j3BBfMgdgFYvM130_provenance a np:Provenance .
  
  dgn-np:NP901564.RA62PfNrMMnmLIzV7HAVpc3YkfOyfmZ8j3BBfMgdgFYvM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP901564.RA62PfNrMMnmLIzV7HAVpc3YkfOyfmZ8j3BBfMgdgFYvM130_assertion {
  miriam-gene:2235 a ncit:C16612 .
  
  lld:C0025517 a ncit:C7057 .
  
  dgn-gda:DGN81a26719b3dbf8a654cf3ab5740685ef sio:SIO_000628 miriam-gene:2235, lld:C0025517;
    a sio:SIO_001121 .
}

dgn-np:NP901564.RA62PfNrMMnmLIzV7HAVpc3YkfOyfmZ8j3BBfMgdgFYvM130_provenance {
  dgn-np:NP901564.RA62PfNrMMnmLIzV7HAVpc3YkfOyfmZ8j3BBfMgdgFYvM130_assertion dcterms:description
      "[Protoporphyria is an inherited disorder of heme biosynthesis characterized by an overproduction of protoporphyrin in the erythropoietic and hepatic tissues, the relative contribution of which in the metabolic disorder has not been directly quantitated.]. 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:3294082;
    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:NP901564.RA62PfNrMMnmLIzV7HAVpc3YkfOyfmZ8j3BBfMgdgFYvM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:14+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" .
}