@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP592419.RAifSa9HhCC0hfL74r-tESfSy_TYVEPvYBeF03VoGlVe8> .
@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:NP592419.RAifSa9HhCC0hfL74r-tESfSy_TYVEPvYBeF03VoGlVe8130_head {
  this: np:hasAssertion dgn-np:NP592419.RAifSa9HhCC0hfL74r-tESfSy_TYVEPvYBeF03VoGlVe8130_assertion ;
    np:hasProvenance dgn-np:NP592419.RAifSa9HhCC0hfL74r-tESfSy_TYVEPvYBeF03VoGlVe8130_provenance ;
    np:hasPublicationInfo dgn-np:NP592419.RAifSa9HhCC0hfL74r-tESfSy_TYVEPvYBeF03VoGlVe8130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP592419.RAifSa9HhCC0hfL74r-tESfSy_TYVEPvYBeF03VoGlVe8130_assertion a np:Assertion .
  dgn-np:NP592419.RAifSa9HhCC0hfL74r-tESfSy_TYVEPvYBeF03VoGlVe8130_provenance a np:Provenance .
  dgn-np:NP592419.RAifSa9HhCC0hfL74r-tESfSy_TYVEPvYBeF03VoGlVe8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP592419.RAifSa9HhCC0hfL74r-tESfSy_TYVEPvYBeF03VoGlVe8130_assertion {
  miriam-gene:23771 a ncit:C16612 .
  lld:C0017668 a ncit:C7057 .
  dgn-gda:DGN1eae38ff1692a7b36549804d08154ee9 sio:SIO_000628 miriam-gene:23771 , lld:C0017668 ;
    a sio:SIO_001121 .
}
dgn-np:NP592419.RAifSa9HhCC0hfL74r-tESfSy_TYVEPvYBeF03VoGlVe8130_provenance {
  dgn-np:NP592419.RAifSa9HhCC0hfL74r-tESfSy_TYVEPvYBeF03VoGlVe8130_assertion dcterms:description "[Sera obtained from control patients or those with minimal change nephrotic syndrome or diabetic nephropathy that was processed in the same manner as FSGS samples had no effect NO synthesis or iNOS activity.]. 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:10198566 ;
    prov:wasDerivedFrom dgn-void:befree-20140225 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP592419.RAifSa9HhCC0hfL74r-tESfSy_TYVEPvYBeF03VoGlVe8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:56+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" .
}