@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP601747.RAuTqJ9Qa7K3aUNn8UEYAEo34gMxKj_Jc82EqnGmKISQc> .
@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/v4.0.0/void/> .
dgn-np:NP601747.RAuTqJ9Qa7K3aUNn8UEYAEo34gMxKj_Jc82EqnGmKISQc130_head {
  this: np:hasAssertion dgn-np:NP601747.RAuTqJ9Qa7K3aUNn8UEYAEo34gMxKj_Jc82EqnGmKISQc130_assertion ;
    np:hasProvenance dgn-np:NP601747.RAuTqJ9Qa7K3aUNn8UEYAEo34gMxKj_Jc82EqnGmKISQc130_provenance ;
    np:hasPublicationInfo dgn-np:NP601747.RAuTqJ9Qa7K3aUNn8UEYAEo34gMxKj_Jc82EqnGmKISQc130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP601747.RAuTqJ9Qa7K3aUNn8UEYAEo34gMxKj_Jc82EqnGmKISQc130_provenance a np:Provenance .
  dgn-np:NP601747.RAuTqJ9Qa7K3aUNn8UEYAEo34gMxKj_Jc82EqnGmKISQc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP601747.RAuTqJ9Qa7K3aUNn8UEYAEo34gMxKj_Jc82EqnGmKISQc130_assertion {
  miriam-gene:1080 a ncit:C16612 .
  lld:C0403814 a ncit:C7057 .
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}
dgn-np:NP601747.RAuTqJ9Qa7K3aUNn8UEYAEo34gMxKj_Jc82EqnGmKISQc130_provenance {
  dgn-np:NP601747.RAuTqJ9Qa7K3aUNn8UEYAEo34gMxKj_Jc82EqnGmKISQc130_assertion dcterms:description "[This manuscript reviews the frequencies, symptoms, testing, and reporting of genotypes with the 5T polythymidine tract which reduces splicing efficiency in the cystic fibrosis transmembrane conductance regulator (CFTR) gene in congenital bilateral absence of the vas deferens (CBAVD) patients and in patients and fetuses with cystic fibrosis-like symptoms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^xsd:date .
  dgn-void:source_evidence_literature a eco:ECO_0000212 ;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
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}
dgn-np:NP601747.RAuTqJ9Qa7K3aUNn8UEYAEo34gMxKj_Jc82EqnGmKISQc130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:18+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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    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> ;
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}