@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP355752.RAavPA8fPM2c20OZTBjS7wcVd257h2YHzCus37xYOxTXA> .
@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:NP355752.RAavPA8fPM2c20OZTBjS7wcVd257h2YHzCus37xYOxTXA130_head {
  this: np:hasAssertion dgn-np:NP355752.RAavPA8fPM2c20OZTBjS7wcVd257h2YHzCus37xYOxTXA130_assertion;
    np:hasProvenance dgn-np:NP355752.RAavPA8fPM2c20OZTBjS7wcVd257h2YHzCus37xYOxTXA130_provenance;
    np:hasPublicationInfo dgn-np:NP355752.RAavPA8fPM2c20OZTBjS7wcVd257h2YHzCus37xYOxTXA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP355752.RAavPA8fPM2c20OZTBjS7wcVd257h2YHzCus37xYOxTXA130_assertion a np:Assertion .
  
  dgn-np:NP355752.RAavPA8fPM2c20OZTBjS7wcVd257h2YHzCus37xYOxTXA130_provenance a np:Provenance .
  
  dgn-np:NP355752.RAavPA8fPM2c20OZTBjS7wcVd257h2YHzCus37xYOxTXA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP355752.RAavPA8fPM2c20OZTBjS7wcVd257h2YHzCus37xYOxTXA130_assertion {
  miriam-gene:2591 a ncit:C16612 .
  
  lld:C0085681 a ncit:C7057 .
  
  dgn-gda:DGN3476f157dea343cbb5f7f2fb87bce988 sio:SIO_000628 miriam-gene:2591, lld:C0085681;
    a sio:SIO_001121 .
}

dgn-np:NP355752.RAavPA8fPM2c20OZTBjS7wcVd257h2YHzCus37xYOxTXA130_provenance {
  dgn-np:NP355752.RAavPA8fPM2c20OZTBjS7wcVd257h2YHzCus37xYOxTXA130_assertion dcterms:description
      "[The elucidation of the molecular basis of HFTC shed new light upon the mechanisms regulating phosphate homeostasis, suggesting innovative therapeutic strategies for the management of hyperphosphatemia in common acquired conditions such as chronic renal failure.]. 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:19013236;
    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:NP355752.RAavPA8fPM2c20OZTBjS7wcVd257h2YHzCus37xYOxTXA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:28+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" .
}