Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP651309.RAa7Fp9rAJQLUcZfP2qKQDigE8N-iF7KRdruMJVoZeNcI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP651309.RAa7Fp9rAJQLUcZfP2qKQDigE8N-iF7KRdruMJVoZeNcI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP651309.RAa7Fp9rAJQLUcZfP2qKQDigE8N-iF7KRdruMJVoZeNcI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP651309.RAa7Fp9rAJQLUcZfP2qKQDigE8N-iF7KRdruMJVoZeNcI130_provenance.
- NP651309.RAa7Fp9rAJQLUcZfP2qKQDigE8N-iF7KRdruMJVoZeNcI130_assertion description "[Approximately 10% to 15% of paragangliomas are caused by mutations in the succinate dehydrogenase (SDH) genes B, C, or D. These are often multifocal as part of paraganglioma syndromes and hormone secreting, and malignant particularly associated with mutations in SDHB.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP651309.RAa7Fp9rAJQLUcZfP2qKQDigE8N-iF7KRdruMJVoZeNcI130_provenance.
- NP651309.RAa7Fp9rAJQLUcZfP2qKQDigE8N-iF7KRdruMJVoZeNcI130_assertion evidence source_evidence_literature NP651309.RAa7Fp9rAJQLUcZfP2qKQDigE8N-iF7KRdruMJVoZeNcI130_provenance.
- NP651309.RAa7Fp9rAJQLUcZfP2qKQDigE8N-iF7KRdruMJVoZeNcI130_assertion SIO_000772 18213727 NP651309.RAa7Fp9rAJQLUcZfP2qKQDigE8N-iF7KRdruMJVoZeNcI130_provenance.
- NP651309.RAa7Fp9rAJQLUcZfP2qKQDigE8N-iF7KRdruMJVoZeNcI130_assertion wasDerivedFrom befree-2016 NP651309.RAa7Fp9rAJQLUcZfP2qKQDigE8N-iF7KRdruMJVoZeNcI130_provenance.
- NP651309.RAa7Fp9rAJQLUcZfP2qKQDigE8N-iF7KRdruMJVoZeNcI130_assertion wasGeneratedBy ECO_0000203 NP651309.RAa7Fp9rAJQLUcZfP2qKQDigE8N-iF7KRdruMJVoZeNcI130_provenance.
- befree-2016 importedOn "2016-02-19" NP651309.RAa7Fp9rAJQLUcZfP2qKQDigE8N-iF7KRdruMJVoZeNcI130_provenance.