Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP775853.RAGLSXGPWz10nWuXk9_Z-UAR_42m55TuvzcgUNr5iEt8A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP775853.RAGLSXGPWz10nWuXk9_Z-UAR_42m55TuvzcgUNr5iEt8A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP775853.RAGLSXGPWz10nWuXk9_Z-UAR_42m55TuvzcgUNr5iEt8A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP775853.RAGLSXGPWz10nWuXk9_Z-UAR_42m55TuvzcgUNr5iEt8A130_provenance.
- NP775853.RAGLSXGPWz10nWuXk9_Z-UAR_42m55TuvzcgUNr5iEt8A130_assertion description "[The paraganglioma-pheochromocytoma syndrome is caused by germline-inactivating mutations in the mitochondrial succinate dehydrogenase (SDH) genes SDHB, SDHC, SDHD, or SDHAF2, and VHL is the result of inactivating VHL gene mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP775853.RAGLSXGPWz10nWuXk9_Z-UAR_42m55TuvzcgUNr5iEt8A130_provenance.
- NP775853.RAGLSXGPWz10nWuXk9_Z-UAR_42m55TuvzcgUNr5iEt8A130_assertion evidence source_evidence_literature NP775853.RAGLSXGPWz10nWuXk9_Z-UAR_42m55TuvzcgUNr5iEt8A130_provenance.
- NP775853.RAGLSXGPWz10nWuXk9_Z-UAR_42m55TuvzcgUNr5iEt8A130_assertion SIO_000772 19915015 NP775853.RAGLSXGPWz10nWuXk9_Z-UAR_42m55TuvzcgUNr5iEt8A130_provenance.
- NP775853.RAGLSXGPWz10nWuXk9_Z-UAR_42m55TuvzcgUNr5iEt8A130_assertion wasDerivedFrom befree-2016 NP775853.RAGLSXGPWz10nWuXk9_Z-UAR_42m55TuvzcgUNr5iEt8A130_provenance.
- NP775853.RAGLSXGPWz10nWuXk9_Z-UAR_42m55TuvzcgUNr5iEt8A130_assertion wasGeneratedBy ECO_0000203 NP775853.RAGLSXGPWz10nWuXk9_Z-UAR_42m55TuvzcgUNr5iEt8A130_provenance.
- befree-2016 importedOn "2016-02-19" NP775853.RAGLSXGPWz10nWuXk9_Z-UAR_42m55TuvzcgUNr5iEt8A130_provenance.