Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP431627.RAE4oyOfeczF2nMnO6U1mHxJYjR-Xfl8IR2uZnNppFXNw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP431627.RAE4oyOfeczF2nMnO6U1mHxJYjR-Xfl8IR2uZnNppFXNw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP431627.RAE4oyOfeczF2nMnO6U1mHxJYjR-Xfl8IR2uZnNppFXNw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP431627.RAE4oyOfeczF2nMnO6U1mHxJYjR-Xfl8IR2uZnNppFXNw130_provenance.
- NP431627.RAE4oyOfeczF2nMnO6U1mHxJYjR-Xfl8IR2uZnNppFXNw130_assertion wasGeneratedBy ECO_0000203 NP431627.RAE4oyOfeczF2nMnO6U1mHxJYjR-Xfl8IR2uZnNppFXNw130_provenance.
- NP431627.RAE4oyOfeczF2nMnO6U1mHxJYjR-Xfl8IR2uZnNppFXNw130_assertion wasDerivedFrom befree-20140225 NP431627.RAE4oyOfeczF2nMnO6U1mHxJYjR-Xfl8IR2uZnNppFXNw130_provenance.
- NP431627.RAE4oyOfeczF2nMnO6U1mHxJYjR-Xfl8IR2uZnNppFXNw130_assertion SIO_000772 23206616 NP431627.RAE4oyOfeczF2nMnO6U1mHxJYjR-Xfl8IR2uZnNppFXNw130_provenance.
- NP431627.RAE4oyOfeczF2nMnO6U1mHxJYjR-Xfl8IR2uZnNppFXNw130_assertion evidence source_evidence_literature NP431627.RAE4oyOfeczF2nMnO6U1mHxJYjR-Xfl8IR2uZnNppFXNw130_provenance.
- NP431627.RAE4oyOfeczF2nMnO6U1mHxJYjR-Xfl8IR2uZnNppFXNw130_assertion description "[Genetic studies showed a deletion of exon 1 in the FLCN gene in the index case as well as nine other individuals, including two with clinical phenotypes of pneumothorax and seven who are symptom-free to date.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP431627.RAE4oyOfeczF2nMnO6U1mHxJYjR-Xfl8IR2uZnNppFXNw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP431627.RAE4oyOfeczF2nMnO6U1mHxJYjR-Xfl8IR2uZnNppFXNw130_provenance.