@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP50647.RAePmQyfpbhhg7BcfG0UNV4RVNjWTas-NsbOcXri4l_pA> .
@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:NP50647.RAePmQyfpbhhg7BcfG0UNV4RVNjWTas-NsbOcXri4l_pA130_head {
  this: np:hasAssertion dgn-np:NP50647.RAePmQyfpbhhg7BcfG0UNV4RVNjWTas-NsbOcXri4l_pA130_assertion;
    np:hasProvenance dgn-np:NP50647.RAePmQyfpbhhg7BcfG0UNV4RVNjWTas-NsbOcXri4l_pA130_provenance;
    np:hasPublicationInfo dgn-np:NP50647.RAePmQyfpbhhg7BcfG0UNV4RVNjWTas-NsbOcXri4l_pA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP50647.RAePmQyfpbhhg7BcfG0UNV4RVNjWTas-NsbOcXri4l_pA130_assertion a np:Assertion .
  
  dgn-np:NP50647.RAePmQyfpbhhg7BcfG0UNV4RVNjWTas-NsbOcXri4l_pA130_provenance a np:Provenance .
  
  dgn-np:NP50647.RAePmQyfpbhhg7BcfG0UNV4RVNjWTas-NsbOcXri4l_pA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP50647.RAePmQyfpbhhg7BcfG0UNV4RVNjWTas-NsbOcXri4l_pA130_assertion {
  miriam-gene:7040 a ncit:C16612 .
  
  lld:C0022658 a ncit:C7057 .
  
  dgn-gda:DGN8112217179ae40dd1d621de0fe989516 sio:SIO_000628 miriam-gene:7040, lld:C0022658;
    a sio:SIO_001122 .
}

dgn-np:NP50647.RAePmQyfpbhhg7BcfG0UNV4RVNjWTas-NsbOcXri4l_pA130_provenance {
  dgn-np:NP50647.RAePmQyfpbhhg7BcfG0UNV4RVNjWTas-NsbOcXri4l_pA130_assertion dcterms:description
      "[ Our study suggests that the haplotype reconstruction of TGF-beta1 gene polymorphisms could be more informative than the investigation of single nucleotide polymorphisms for defining the associated risk of developing IgAN. Further research is needed on larger cohorts to confirm TGF-beta1 involvement and test other TGF-beta1 variants with possible additive or synergistic effects.]. 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:15593052;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP50647.RAePmQyfpbhhg7BcfG0UNV4RVNjWTas-NsbOcXri4l_pA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:23+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" .
}