Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP202153.RAEp17WSyAROQDll_zfkUVUT7ZS-F5DGA6N4XzicTATt8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP202153.RAEp17WSyAROQDll_zfkUVUT7ZS-F5DGA6N4XzicTATt8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP202153.RAEp17WSyAROQDll_zfkUVUT7ZS-F5DGA6N4XzicTATt8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP202153.RAEp17WSyAROQDll_zfkUVUT7ZS-F5DGA6N4XzicTATt8130_provenance.
- NP202153.RAEp17WSyAROQDll_zfkUVUT7ZS-F5DGA6N4XzicTATt8130_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." NP202153.RAEp17WSyAROQDll_zfkUVUT7ZS-F5DGA6N4XzicTATt8130_provenance.
- NP202153.RAEp17WSyAROQDll_zfkUVUT7ZS-F5DGA6N4XzicTATt8130_assertion evidence source_evidence_literature NP202153.RAEp17WSyAROQDll_zfkUVUT7ZS-F5DGA6N4XzicTATt8130_provenance.
- NP202153.RAEp17WSyAROQDll_zfkUVUT7ZS-F5DGA6N4XzicTATt8130_assertion SIO_000772 18213727 NP202153.RAEp17WSyAROQDll_zfkUVUT7ZS-F5DGA6N4XzicTATt8130_provenance.
- NP202153.RAEp17WSyAROQDll_zfkUVUT7ZS-F5DGA6N4XzicTATt8130_assertion wasDerivedFrom befree-20140225 NP202153.RAEp17WSyAROQDll_zfkUVUT7ZS-F5DGA6N4XzicTATt8130_provenance.
- NP202153.RAEp17WSyAROQDll_zfkUVUT7ZS-F5DGA6N4XzicTATt8130_assertion wasGeneratedBy ECO_0000203 NP202153.RAEp17WSyAROQDll_zfkUVUT7ZS-F5DGA6N4XzicTATt8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP202153.RAEp17WSyAROQDll_zfkUVUT7ZS-F5DGA6N4XzicTATt8130_provenance.