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- source_evidence_literature type ECO_0000212 NP689117.RAbve5mHsVefMLE8pcGatlZV2hesfBoVD6CF-CvWwTZuM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP689117.RAbve5mHsVefMLE8pcGatlZV2hesfBoVD6CF-CvWwTZuM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP689117.RAbve5mHsVefMLE8pcGatlZV2hesfBoVD6CF-CvWwTZuM130_provenance.
- NP689117.RAbve5mHsVefMLE8pcGatlZV2hesfBoVD6CF-CvWwTZuM130_assertion description "[Up to 30% of pheochromocytomas and paragangliomas are associated with germline RET, Von Hippel-Lindau (VHL), neurofibromatosis type I (NF1), and succinate dehydrogenase subunits (SDHB, SDHC, and SDHD) mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP689117.RAbve5mHsVefMLE8pcGatlZV2hesfBoVD6CF-CvWwTZuM130_provenance.
- NP689117.RAbve5mHsVefMLE8pcGatlZV2hesfBoVD6CF-CvWwTZuM130_assertion evidence source_evidence_literature NP689117.RAbve5mHsVefMLE8pcGatlZV2hesfBoVD6CF-CvWwTZuM130_provenance.
- NP689117.RAbve5mHsVefMLE8pcGatlZV2hesfBoVD6CF-CvWwTZuM130_assertion SIO_000772 20236688 NP689117.RAbve5mHsVefMLE8pcGatlZV2hesfBoVD6CF-CvWwTZuM130_provenance.
- NP689117.RAbve5mHsVefMLE8pcGatlZV2hesfBoVD6CF-CvWwTZuM130_assertion wasDerivedFrom befree-20150227 NP689117.RAbve5mHsVefMLE8pcGatlZV2hesfBoVD6CF-CvWwTZuM130_provenance.
- NP689117.RAbve5mHsVefMLE8pcGatlZV2hesfBoVD6CF-CvWwTZuM130_assertion wasGeneratedBy ECO_0000203 NP689117.RAbve5mHsVefMLE8pcGatlZV2hesfBoVD6CF-CvWwTZuM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP689117.RAbve5mHsVefMLE8pcGatlZV2hesfBoVD6CF-CvWwTZuM130_provenance.