@prefix dc: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1085.RAWfE8TKOBJ6IbP3w5ol-m76YwRj0AKcLagkxT9j3UOac> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP1085.RAWfE8TKOBJ6IbP3w5ol-m76YwRj0AKcLagkxT9j3UOac130_head {
  this: np:hasAssertion dgn-np:NP1085.RAWfE8TKOBJ6IbP3w5ol-m76YwRj0AKcLagkxT9j3UOac130_assertion;
    np:hasProvenance dgn-np:NP1085.RAWfE8TKOBJ6IbP3w5ol-m76YwRj0AKcLagkxT9j3UOac130_provenance;
    np:hasPublicationInfo dgn-np:NP1085.RAWfE8TKOBJ6IbP3w5ol-m76YwRj0AKcLagkxT9j3UOac130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1085.RAWfE8TKOBJ6IbP3w5ol-m76YwRj0AKcLagkxT9j3UOac130_assertion a np:Assertion .
  
  dgn-np:NP1085.RAWfE8TKOBJ6IbP3w5ol-m76YwRj0AKcLagkxT9j3UOac130_provenance a np:Provenance .
  
  dgn-np:NP1085.RAWfE8TKOBJ6IbP3w5ol-m76YwRj0AKcLagkxT9j3UOac130_publicationInfo a np:PublicationInfo .
}

dgn-np:NP1085.RAWfE8TKOBJ6IbP3w5ol-m76YwRj0AKcLagkxT9j3UOac130_assertion {
  miriam-gene:5095 a ncit:C16612 .
  
  lld:C0268579 a ncit:C7057 .
  
  dgn-gda:DGN385bd011367f2191aa1313be6bb77105 sio:SIO_000628 miriam-gene:5095, lld:C0268579;
    a sio:SIO_001122 .
}

dgn-np:NP1085.RAWfE8TKOBJ6IbP3w5ol-m76YwRj0AKcLagkxT9j3UOac130_provenance {
  dgn-np:NP1085.RAWfE8TKOBJ6IbP3w5ol-m76YwRj0AKcLagkxT9j3UOac130_assertion dc:description
      "[The inherited metabolic disease propionic acidemia (PA) can result from mutations in either of the genes PCCA or PCCB, which encode the alpha and beta subunits, respectively, of the mitochondrial enzyme propionyl CoA-carboxylase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_curated;
    sio:SIO_000772 miriam-pubmed:10101253;
    prov:wasDerivedFrom dgn-void:uniprot-20150221;
    prov:wasGeneratedBy eco:ECO_0000218 .
  
  dgn-void:source_evidence_curated a eco:ECO_0000205;
    rdfs:comment "Gene-disease associations manually curated."@en;
    rdfs:label "DisGeNET evidence - CURATED"@en .
  
  dgn-void:uniprot-20150221 pav:importedOn "2015-02-21"^^xsd:date .
}

dgn-np:NP1085.RAWfE8TKOBJ6IbP3w5ol-m76YwRj0AKcLagkxT9j3UOac130_publicationInfo {
  this: dc:created "2015-08-25T14:37:42+02:00"^^xsd:dateTime;
    dc:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dc:rightsHolder dgn-void:IBIGroup;
    dc:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetv3.0rdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}