@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP399811.RAafxGQ-yhZ8k98O0_B3y0hgcYNk9tJweX3iTNjST0b3g130_head { this: np:hasAssertion dgn-np:NP399811.RAafxGQ-yhZ8k98O0_B3y0hgcYNk9tJweX3iTNjST0b3g130_assertion; np:hasProvenance dgn-np:NP399811.RAafxGQ-yhZ8k98O0_B3y0hgcYNk9tJweX3iTNjST0b3g130_provenance; np:hasPublicationInfo dgn-np:NP399811.RAafxGQ-yhZ8k98O0_B3y0hgcYNk9tJweX3iTNjST0b3g130_publicationInfo; a np:Nanopublication . dgn-np:NP399811.RAafxGQ-yhZ8k98O0_B3y0hgcYNk9tJweX3iTNjST0b3g130_assertion a np:Assertion . dgn-np:NP399811.RAafxGQ-yhZ8k98O0_B3y0hgcYNk9tJweX3iTNjST0b3g130_provenance a np:Provenance . dgn-np:NP399811.RAafxGQ-yhZ8k98O0_B3y0hgcYNk9tJweX3iTNjST0b3g130_publicationInfo a np:PublicationInfo . } dgn-np:NP399811.RAafxGQ-yhZ8k98O0_B3y0hgcYNk9tJweX3iTNjST0b3g130_assertion { miriam-gene:1080 a ncit:C16612 . lld:C0010674 a ncit:C7057 . dgn-gda:DGNbe2f84fc94b87bd7123b0ac512f20278 sio:SIO_000628 miriam-gene:1080, lld:C0010674; a sio:SIO_001121 . } dgn-np:NP399811.RAafxGQ-yhZ8k98O0_B3y0hgcYNk9tJweX3iTNjST0b3g130_provenance { dgn-np:NP399811.RAafxGQ-yhZ8k98O0_B3y0hgcYNk9tJweX3iTNjST0b3g130_assertion dcterms:description "[German patients with cystic fibrosis (CF) were screened for molecular lesions in exon 13 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene by single strand conformation polymorphism (SSCP) and chemical cleavage of mismatch analyses.]. 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:1283149; 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; rdfs:label "DisGeNET evidence - LITERATURE"@en . } dgn-np:NP399811.RAafxGQ-yhZ8k98O0_B3y0hgcYNk9tJweX3iTNjST0b3g130_publicationInfo { this: dcterms:created "2016-05-13T12:44:46+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }