@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP393980.RARLeQ7hf_kRaN_jRkBOTsQd7aCGd-1f0MHs8PsXtRycs> .
@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:NP393980.RARLeQ7hf_kRaN_jRkBOTsQd7aCGd-1f0MHs8PsXtRycs130_head {
  this: np:hasAssertion dgn-np:NP393980.RARLeQ7hf_kRaN_jRkBOTsQd7aCGd-1f0MHs8PsXtRycs130_assertion ;
    np:hasProvenance dgn-np:NP393980.RARLeQ7hf_kRaN_jRkBOTsQd7aCGd-1f0MHs8PsXtRycs130_provenance ;
    np:hasPublicationInfo dgn-np:NP393980.RARLeQ7hf_kRaN_jRkBOTsQd7aCGd-1f0MHs8PsXtRycs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP393980.RARLeQ7hf_kRaN_jRkBOTsQd7aCGd-1f0MHs8PsXtRycs130_assertion a np:Assertion .
  dgn-np:NP393980.RARLeQ7hf_kRaN_jRkBOTsQd7aCGd-1f0MHs8PsXtRycs130_provenance a np:Provenance .
  dgn-np:NP393980.RARLeQ7hf_kRaN_jRkBOTsQd7aCGd-1f0MHs8PsXtRycs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP393980.RARLeQ7hf_kRaN_jRkBOTsQd7aCGd-1f0MHs8PsXtRycs130_assertion {
  miriam-gene:5498 a ncit:C16612 .
  lld:C0162531 a ncit:C7057 .
  dgn-gda:DGNc35f6c069d2d46d29250ab686d6771b0 sio:SIO_000628 miriam-gene:5498 , lld:C0162531 ;
    a sio:SIO_001121 .
}
dgn-np:NP393980.RARLeQ7hf_kRaN_jRkBOTsQd7aCGd-1f0MHs8PsXtRycs130_provenance {
  dgn-np:NP393980.RARLeQ7hf_kRaN_jRkBOTsQd7aCGd-1f0MHs8PsXtRycs130_assertion dcterms:description "[There are seven main types of porphyrias; acute intermittent porphyria and plumboporphyria are predominantly neuropsychiatric; congenital erythropoietic porphyria, porphyria cutanea tarda and erythropoietic protoporphyria have predominantly cutaneous manifestations and hereditary coproporphyria and variegate porphyria are classified as mixed as they both have neuropsychiatric and cutaneous features.]. 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:18541093 ;
    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:NP393980.RARLeQ7hf_kRaN_jRkBOTsQd7aCGd-1f0MHs8PsXtRycs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:54+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" .
}