@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP25764.RA7kIxp9ZBQ6gnNVD9xtOAiV_M0qniImdsZxvD9TDeZiE> .
@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:NP25764.RA7kIxp9ZBQ6gnNVD9xtOAiV_M0qniImdsZxvD9TDeZiE130_head {
  this: np:hasAssertion dgn-np:NP25764.RA7kIxp9ZBQ6gnNVD9xtOAiV_M0qniImdsZxvD9TDeZiE130_assertion;
    np:hasProvenance dgn-np:NP25764.RA7kIxp9ZBQ6gnNVD9xtOAiV_M0qniImdsZxvD9TDeZiE130_provenance;
    np:hasPublicationInfo dgn-np:NP25764.RA7kIxp9ZBQ6gnNVD9xtOAiV_M0qniImdsZxvD9TDeZiE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP25764.RA7kIxp9ZBQ6gnNVD9xtOAiV_M0qniImdsZxvD9TDeZiE130_assertion a np:Assertion .
  
  dgn-np:NP25764.RA7kIxp9ZBQ6gnNVD9xtOAiV_M0qniImdsZxvD9TDeZiE130_provenance a np:Provenance .
  
  dgn-np:NP25764.RA7kIxp9ZBQ6gnNVD9xtOAiV_M0qniImdsZxvD9TDeZiE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP25764.RA7kIxp9ZBQ6gnNVD9xtOAiV_M0qniImdsZxvD9TDeZiE130_assertion {
  miriam-gene:5194 a ncit:C16612 .
  
  lld:C1832200 a ncit:C7057 .
  
  dgn-gda:DGN92c084fde051c017a7263fc050e0433e sio:SIO_000628 miriam-gene:5194, lld:C1832200;
    a sio:SIO_001121 .
}

dgn-np:NP25764.RA7kIxp9ZBQ6gnNVD9xtOAiV_M0qniImdsZxvD9TDeZiE130_provenance {
  dgn-np:NP25764.RA7kIxp9ZBQ6gnNVD9xtOAiV_M0qniImdsZxvD9TDeZiE130_assertion dcterms:description
      "[We now have evidence that the complete human cDNA encoding Pex13p, an SH3 protein of a docking factor for the peroxisome targeting signal 1 receptor (Pex5p), rescues peroxisomal matrix protein import and its assembly in fibroblasts from PBD patients of complementation group H. In addition, we detected mutations on the human PEX13 cDNA in two patients of group H. A severe phenotype of a ZS patient (H-02) was homozygous for a nonsense mutation, W234ter, which results in the loss of not only the SH3 domain but also the putative transmembrane domain of Pex13p.]. 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:10332040;
    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:NP25764.RA7kIxp9ZBQ6gnNVD9xtOAiV_M0qniImdsZxvD9TDeZiE130_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" .
}