@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP147430.RAARMa2KcFaD2RwJ7aqrM-PLwLMJ1IJTCeQv7aHhfr18Y> .
@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:NP147430.RAARMa2KcFaD2RwJ7aqrM-PLwLMJ1IJTCeQv7aHhfr18Y130_head {
  this: np:hasAssertion dgn-np:NP147430.RAARMa2KcFaD2RwJ7aqrM-PLwLMJ1IJTCeQv7aHhfr18Y130_assertion;
    np:hasProvenance dgn-np:NP147430.RAARMa2KcFaD2RwJ7aqrM-PLwLMJ1IJTCeQv7aHhfr18Y130_provenance;
    np:hasPublicationInfo dgn-np:NP147430.RAARMa2KcFaD2RwJ7aqrM-PLwLMJ1IJTCeQv7aHhfr18Y130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP147430.RAARMa2KcFaD2RwJ7aqrM-PLwLMJ1IJTCeQv7aHhfr18Y130_assertion a np:Assertion .
  
  dgn-np:NP147430.RAARMa2KcFaD2RwJ7aqrM-PLwLMJ1IJTCeQv7aHhfr18Y130_provenance a np:Provenance .
  
  dgn-np:NP147430.RAARMa2KcFaD2RwJ7aqrM-PLwLMJ1IJTCeQv7aHhfr18Y130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP147430.RAARMa2KcFaD2RwJ7aqrM-PLwLMJ1IJTCeQv7aHhfr18Y130_assertion {
  miriam-gene:7356 a ncit:C16612 .
  
  lld:C0017661 a ncit:C7057 .
  
  dgn-gda:DGNbdb6c6f3ddc5f83a186d59c8ac5644d8 sio:SIO_000628 miriam-gene:7356, lld:C0017661;
    a sio:SIO_001122 .
}

dgn-np:NP147430.RAARMa2KcFaD2RwJ7aqrM-PLwLMJ1IJTCeQv7aHhfr18Y130_provenance {
  dgn-np:NP147430.RAARMa2KcFaD2RwJ7aqrM-PLwLMJ1IJTCeQv7aHhfr18Y130_assertion dcterms:description
      "[The effect of G38A may be apparent under stimulation as sex steroids or infections, and homozygotes of the G38A mutation cannot produce sufficient UG in response to stimulation and may be predisposed to IgA nephropathy, especially in childhood.]. 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:11774099;
    prov:wasDerivedFrom dgn-void:lhgdn-20090331;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:lhgdn-20090331 pav:importedOn "2009-03-31"^^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:NP147430.RAARMa2KcFaD2RwJ7aqrM-PLwLMJ1IJTCeQv7aHhfr18Y130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:17+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" .
}