@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP869958.RAWDcVdUKpwrxbZd9uj4NGgqd7tmRi2Y3Pg7qSYN_aGFQ> .
@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:NP869958.RAWDcVdUKpwrxbZd9uj4NGgqd7tmRi2Y3Pg7qSYN_aGFQ130_head {
  this: np:hasAssertion dgn-np:NP869958.RAWDcVdUKpwrxbZd9uj4NGgqd7tmRi2Y3Pg7qSYN_aGFQ130_assertion ;
    np:hasProvenance dgn-np:NP869958.RAWDcVdUKpwrxbZd9uj4NGgqd7tmRi2Y3Pg7qSYN_aGFQ130_provenance ;
    np:hasPublicationInfo dgn-np:NP869958.RAWDcVdUKpwrxbZd9uj4NGgqd7tmRi2Y3Pg7qSYN_aGFQ130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP869958.RAWDcVdUKpwrxbZd9uj4NGgqd7tmRi2Y3Pg7qSYN_aGFQ130_assertion a np:Assertion .
  dgn-np:NP869958.RAWDcVdUKpwrxbZd9uj4NGgqd7tmRi2Y3Pg7qSYN_aGFQ130_provenance a np:Provenance .
  dgn-np:NP869958.RAWDcVdUKpwrxbZd9uj4NGgqd7tmRi2Y3Pg7qSYN_aGFQ130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP869958.RAWDcVdUKpwrxbZd9uj4NGgqd7tmRi2Y3Pg7qSYN_aGFQ130_assertion {
  miriam-gene:210 a ncit:C16612 .
  lld:C0162565 a ncit:C7057 .
  dgn-gda:DGN0b6c4167c9effcb36ad2a757e89c044b sio:SIO_000628 miriam-gene:210 , lld:C0162565 ;
    a sio:SIO_001121 .
}
dgn-np:NP869958.RAWDcVdUKpwrxbZd9uj4NGgqd7tmRi2Y3Pg7qSYN_aGFQ130_provenance {
  dgn-np:NP869958.RAWDcVdUKpwrxbZd9uj4NGgqd7tmRi2Y3Pg7qSYN_aGFQ130_assertion dcterms:description "[1. delta-Aminolevulinic acid dehydratase (ALA-D), blood lead and several enzymes and metabolites of the heme biosynthetic pathway were measured in a number of symptomatic porphyric patients, 22 with acute intermittent porphyria, three with hereditary hepatic coproporphyria, 10 with hereditary porphyria cutanea tarda, two with erythropoietic protoporphyria and two with congenital erythropoietic porphyria and in 84 lead intoxicated persons.]. 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:3622905 ;
    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:NP869958.RAWDcVdUKpwrxbZd9uj4NGgqd7tmRi2Y3Pg7qSYN_aGFQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:52+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" .
}