@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP3035.RACZzruQGABCKat9Hs8HEEyctvrxaRS1jF83hQEO0abrA> .
@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 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:NP3035.RACZzruQGABCKat9Hs8HEEyctvrxaRS1jF83hQEO0abrA130_head {
  this: np:hasAssertion dgn-np:NP3035.RACZzruQGABCKat9Hs8HEEyctvrxaRS1jF83hQEO0abrA130_assertion;
    np:hasProvenance dgn-np:NP3035.RACZzruQGABCKat9Hs8HEEyctvrxaRS1jF83hQEO0abrA130_provenance;
    np:hasPublicationInfo dgn-np:NP3035.RACZzruQGABCKat9Hs8HEEyctvrxaRS1jF83hQEO0abrA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP3035.RACZzruQGABCKat9Hs8HEEyctvrxaRS1jF83hQEO0abrA130_assertion a np:Assertion .
  
  dgn-np:NP3035.RACZzruQGABCKat9Hs8HEEyctvrxaRS1jF83hQEO0abrA130_provenance a np:Provenance .
  
  dgn-np:NP3035.RACZzruQGABCKat9Hs8HEEyctvrxaRS1jF83hQEO0abrA130_publicationInfo a np:PublicationInfo .
}

dgn-np:NP3035.RACZzruQGABCKat9Hs8HEEyctvrxaRS1jF83hQEO0abrA130_assertion {
  miriam-gene:3145 a ncit:C16612 .
  
  lld:C0162565 a ncit:C7057 .
  
  dgn-gda:DGNde063e0ac9dc6d02c60c03b6c672a97e sio:SIO_000628 miriam-gene:3145, lld:C0162565;
    a sio:SIO_001122 .
}

dgn-np:NP3035.RACZzruQGABCKat9Hs8HEEyctvrxaRS1jF83hQEO0abrA130_provenance {
  dgn-np:NP3035.RACZzruQGABCKat9Hs8HEEyctvrxaRS1jF83hQEO0abrA130_assertion dcterms:description
      "[To study the origin of these common CpG mutations, eight intragenic single-nucleotide polymorphisms (SNPs) in the PBGD gene, as well as eight microsatellites flanking the gene in chromosome 11 were used to construct haplotypes in six AIP families of German, Polish and Swiss origins who carried either G111R (4707G>A) or R173Q (6391G>A) mutations.]. 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:15669678;
    prov:wasDerivedFrom dgn-void:uniprot-20130724;
    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-20130724 pav:importedOn "2013-07-24"^^xsd:date .
}

dgn-np:NP3035.RACZzruQGABCKat9Hs8HEEyctvrxaRS1jF83hQEO0abrA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:31:59+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" .
}