@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP25580.RAmT2YeM8dc2eu_5840aU6ZTLj0XNFt8Xqi6Z_wCX-csM> .
@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:NP25580.RAmT2YeM8dc2eu_5840aU6ZTLj0XNFt8Xqi6Z_wCX-csM130_head {
  this: np:hasAssertion dgn-np:NP25580.RAmT2YeM8dc2eu_5840aU6ZTLj0XNFt8Xqi6Z_wCX-csM130_assertion;
    np:hasProvenance dgn-np:NP25580.RAmT2YeM8dc2eu_5840aU6ZTLj0XNFt8Xqi6Z_wCX-csM130_provenance;
    np:hasPublicationInfo dgn-np:NP25580.RAmT2YeM8dc2eu_5840aU6ZTLj0XNFt8Xqi6Z_wCX-csM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP25580.RAmT2YeM8dc2eu_5840aU6ZTLj0XNFt8Xqi6Z_wCX-csM130_assertion a np:Assertion .
  
  dgn-np:NP25580.RAmT2YeM8dc2eu_5840aU6ZTLj0XNFt8Xqi6Z_wCX-csM130_provenance a np:Provenance .
  
  dgn-np:NP25580.RAmT2YeM8dc2eu_5840aU6ZTLj0XNFt8Xqi6Z_wCX-csM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP25580.RAmT2YeM8dc2eu_5840aU6ZTLj0XNFt8Xqi6Z_wCX-csM130_assertion {
  miriam-gene:5145 a ncit:C16612 .
  
  lld:C0035334 a ncit:C7057 .
  
  dgn-gda:DGN349523156846cb4ab787527fa28143f7 sio:SIO_000628 miriam-gene:5145, lld:C0035334;
    a sio:SIO_001121 .
}

dgn-np:NP25580.RAmT2YeM8dc2eu_5840aU6ZTLj0XNFt8Xqi6Z_wCX-csM130_provenance {
  dgn-np:NP25580.RAmT2YeM8dc2eu_5840aU6ZTLj0XNFt8Xqi6Z_wCX-csM130_assertion dcterms:description
      "[As null mutations in PDEB cause some cases of RP and since both alpha and beta subunits are required for full phosphodiesterase activity, we examined the gene encoding the alpha subunit of cGMP phosphodiesterase (PDEA) in 340 unrelated patients with RP.]. 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:7493036;
    prov:wasDerivedFrom dgn-void:ctd_human-20130708;
    prov:wasGeneratedBy eco:ECO_0000218 .
  
  dgn-void:ctd_human-20130708 pav:importedOn "2013-07-24"^^xsd:date .
  
  dgn-void:source_evidence_curated a eco:ECO_0000205;
    rdfs:comment "Gene-disease associations manually curated."@en;
    rdfs:label "DisGeNET evidence - CURATED"@en .
}

dgn-np:NP25580.RAmT2YeM8dc2eu_5840aU6ZTLj0XNFt8Xqi6Z_wCX-csM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:10+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" .
}