@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP860459.RAmf3oNpEOx30P-JDxko_hugAOv7Zx0Ufa1eq9EXqK0HQ> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP860459.RAmf3oNpEOx30P-JDxko_hugAOv7Zx0Ufa1eq9EXqK0HQ130_head {
  this: np:hasAssertion dgn-np:NP860459.RAmf3oNpEOx30P-JDxko_hugAOv7Zx0Ufa1eq9EXqK0HQ130_assertion;
    np:hasProvenance dgn-np:NP860459.RAmf3oNpEOx30P-JDxko_hugAOv7Zx0Ufa1eq9EXqK0HQ130_provenance;
    np:hasPublicationInfo dgn-np:NP860459.RAmf3oNpEOx30P-JDxko_hugAOv7Zx0Ufa1eq9EXqK0HQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP860459.RAmf3oNpEOx30P-JDxko_hugAOv7Zx0Ufa1eq9EXqK0HQ130_assertion a np:Assertion .
  
  dgn-np:NP860459.RAmf3oNpEOx30P-JDxko_hugAOv7Zx0Ufa1eq9EXqK0HQ130_provenance a np:Provenance .
  
  dgn-np:NP860459.RAmf3oNpEOx30P-JDxko_hugAOv7Zx0Ufa1eq9EXqK0HQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP860459.RAmf3oNpEOx30P-JDxko_hugAOv7Zx0Ufa1eq9EXqK0HQ130_assertion {
  miriam-gene:11136 a ncit:C16612 .
  
  lld:C0018609 a ncit:C7057 .
  
  dgn-gda:DGN8e752de6c6e034fea5b93362f53992e0 sio:SIO_000628 miriam-gene:11136, lld:C0018609;
    a sio:SIO_001122 .
}

dgn-np:NP860459.RAmf3oNpEOx30P-JDxko_hugAOv7Zx0Ufa1eq9EXqK0HQ130_provenance {
  dgn-np:NP860459.RAmf3oNpEOx30P-JDxko_hugAOv7Zx0Ufa1eq9EXqK0HQ130_assertion dcterms:description
      "[We thus show that ACE2 is necessary for the expression of the Hartnup transporter in intestine and suggest that the differential functional association of mutant B(0)AT1 transporters with ACE2 and collectrin in intestine and kidney, respectively, participates in the phenotypic heterogeneity of human Hartnup disorder.]. 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:19185582;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP860459.RAmf3oNpEOx30P-JDxko_hugAOv7Zx0Ufa1eq9EXqK0HQ130_publicationInfo {
  this: dcterms:created "2015-08-25T14:46:22+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}