@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP928252.RAqInoCLFU8N3a9B_5ln68k4PVbVHb6exrKJKzk7BfU50> .
@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:NP928252.RAqInoCLFU8N3a9B_5ln68k4PVbVHb6exrKJKzk7BfU50130_head {
  this: np:hasAssertion dgn-np:NP928252.RAqInoCLFU8N3a9B_5ln68k4PVbVHb6exrKJKzk7BfU50130_assertion;
    np:hasProvenance dgn-np:NP928252.RAqInoCLFU8N3a9B_5ln68k4PVbVHb6exrKJKzk7BfU50130_provenance;
    np:hasPublicationInfo dgn-np:NP928252.RAqInoCLFU8N3a9B_5ln68k4PVbVHb6exrKJKzk7BfU50130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP928252.RAqInoCLFU8N3a9B_5ln68k4PVbVHb6exrKJKzk7BfU50130_assertion a np:Assertion .
  
  dgn-np:NP928252.RAqInoCLFU8N3a9B_5ln68k4PVbVHb6exrKJKzk7BfU50130_provenance a np:Provenance .
  
  dgn-np:NP928252.RAqInoCLFU8N3a9B_5ln68k4PVbVHb6exrKJKzk7BfU50130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP928252.RAqInoCLFU8N3a9B_5ln68k4PVbVHb6exrKJKzk7BfU50130_assertion {
  miriam-gene:4582 a ncit:C16612 .
  
  lld:C0010674 a ncit:C7057 .
  
  dgn-gda:DGN631e22327cbb54e598a0e20acbb496fa sio:SIO_000628 miriam-gene:4582, lld:C0010674;
    a sio:SIO_001121 .
}

dgn-np:NP928252.RAqInoCLFU8N3a9B_5ln68k4PVbVHb6exrKJKzk7BfU50130_provenance {
  dgn-np:NP928252.RAqInoCLFU8N3a9B_5ln68k4PVbVHb6exrKJKzk7BfU50130_assertion dcterms:description
      "[The potentiator Kalydeco™ (also known as Ivacaftor or VX-770), developed by Vertex Pharmaceuticals, has been recently approved by the US FDA and the European Medicines Agency (EMA) for the treatment of CF patients carrying at least one CFTR allele with the p.Gly551Asp mutation (2-5 % of all patients).]. 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:23757197;
    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:NP928252.RAqInoCLFU8N3a9B_5ln68k4PVbVHb6exrKJKzk7BfU50130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:29+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" .
}