Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1038319.RASrX0udmHr0nC7lbDfrQtXrMoUJL1h41twGHq823FxAw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1038319.RASrX0udmHr0nC7lbDfrQtXrMoUJL1h41twGHq823FxAw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1038319.RASrX0udmHr0nC7lbDfrQtXrMoUJL1h41twGHq823FxAw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1038319.RASrX0udmHr0nC7lbDfrQtXrMoUJL1h41twGHq823FxAw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1038319.RASrX0udmHr0nC7lbDfrQtXrMoUJL1h41twGHq823FxAw130_provenance.
- NP1038319.RASrX0udmHr0nC7lbDfrQtXrMoUJL1h41twGHq823FxAw130_assertion wasGeneratedBy ECO_0000203 NP1038319.RASrX0udmHr0nC7lbDfrQtXrMoUJL1h41twGHq823FxAw130_provenance.
- NP1038319.RASrX0udmHr0nC7lbDfrQtXrMoUJL1h41twGHq823FxAw130_assertion wasDerivedFrom befree-2016 NP1038319.RASrX0udmHr0nC7lbDfrQtXrMoUJL1h41twGHq823FxAw130_provenance.
- NP1038319.RASrX0udmHr0nC7lbDfrQtXrMoUJL1h41twGHq823FxAw130_assertion SIO_000772 23264078 NP1038319.RASrX0udmHr0nC7lbDfrQtXrMoUJL1h41twGHq823FxAw130_provenance.
- NP1038319.RASrX0udmHr0nC7lbDfrQtXrMoUJL1h41twGHq823FxAw130_assertion evidence source_evidence_literature NP1038319.RASrX0udmHr0nC7lbDfrQtXrMoUJL1h41twGHq823FxAw130_provenance.
- NP1038319.RASrX0udmHr0nC7lbDfrQtXrMoUJL1h41twGHq823FxAw130_assertion description "[Birt-Hogg-Dubé syndrome (BHD) is an autosomal dominant condition due to germline FLCN (folliculin) mutations, characterized by skin fibrofolliculomas, lung cysts, pneumothorax and renal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1038319.RASrX0udmHr0nC7lbDfrQtXrMoUJL1h41twGHq823FxAw130_provenance.