@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP635709.RA_Smf0KprYq7uaDaq1hY2630yI3uA2PKUNI2PVGBVq_I> .
@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:NP635709.RA_Smf0KprYq7uaDaq1hY2630yI3uA2PKUNI2PVGBVq_I130_head {
  this: np:hasAssertion dgn-np:NP635709.RA_Smf0KprYq7uaDaq1hY2630yI3uA2PKUNI2PVGBVq_I130_assertion ;
    np:hasProvenance dgn-np:NP635709.RA_Smf0KprYq7uaDaq1hY2630yI3uA2PKUNI2PVGBVq_I130_provenance ;
    np:hasPublicationInfo dgn-np:NP635709.RA_Smf0KprYq7uaDaq1hY2630yI3uA2PKUNI2PVGBVq_I130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP635709.RA_Smf0KprYq7uaDaq1hY2630yI3uA2PKUNI2PVGBVq_I130_assertion a np:Assertion .
  dgn-np:NP635709.RA_Smf0KprYq7uaDaq1hY2630yI3uA2PKUNI2PVGBVq_I130_provenance a np:Provenance .
  dgn-np:NP635709.RA_Smf0KprYq7uaDaq1hY2630yI3uA2PKUNI2PVGBVq_I130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP635709.RA_Smf0KprYq7uaDaq1hY2630yI3uA2PKUNI2PVGBVq_I130_assertion {
  miriam-gene:4843 a ncit:C16612 .
  lld:C0010674 a ncit:C7057 .
  dgn-gda:DGN10ab1cd0e934c48a0ea76bc2edc448d8 sio:SIO_000628 miriam-gene:4843 , lld:C0010674 ;
    a sio:SIO_001121 .
}
dgn-np:NP635709.RA_Smf0KprYq7uaDaq1hY2630yI3uA2PKUNI2PVGBVq_I130_provenance {
  dgn-np:NP635709.RA_Smf0KprYq7uaDaq1hY2630yI3uA2PKUNI2PVGBVq_I130_assertion dcterms:description "[These complexes effect partial correction of the chloride transport defect as assessed by in vivo nasal potential difference measurements, produce immunohistochemical staining for CFTR, and restore expression of nitric oxide synthase-2 (NOS-2), which is downregulated in the epithelium of mice and humans with cystic fibrosis.]. 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:11945068 ;
    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:NP635709.RA_Smf0KprYq7uaDaq1hY2630yI3uA2PKUNI2PVGBVq_I130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:23+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" .
}