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- NP553195.RAfmt8v6cUQMwdMLu_CatH34tuORwubNLkqD27_OaJLFM130_assertion type Assertion NP553195.RAfmt8v6cUQMwdMLu_CatH34tuORwubNLkqD27_OaJLFM130_head.
- NP553195.RAfmt8v6cUQMwdMLu_CatH34tuORwubNLkqD27_OaJLFM130_assertion wasGeneratedBy ECO_0000203 NP553195.RAfmt8v6cUQMwdMLu_CatH34tuORwubNLkqD27_OaJLFM130_provenance.
- NP553195.RAfmt8v6cUQMwdMLu_CatH34tuORwubNLkqD27_OaJLFM130_assertion wasDerivedFrom befree-20150227 NP553195.RAfmt8v6cUQMwdMLu_CatH34tuORwubNLkqD27_OaJLFM130_provenance.
- NP553195.RAfmt8v6cUQMwdMLu_CatH34tuORwubNLkqD27_OaJLFM130_assertion SIO_000772 22846739 NP553195.RAfmt8v6cUQMwdMLu_CatH34tuORwubNLkqD27_OaJLFM130_provenance.
- NP553195.RAfmt8v6cUQMwdMLu_CatH34tuORwubNLkqD27_OaJLFM130_assertion evidence source_evidence_literature NP553195.RAfmt8v6cUQMwdMLu_CatH34tuORwubNLkqD27_OaJLFM130_provenance.
- NP553195.RAfmt8v6cUQMwdMLu_CatH34tuORwubNLkqD27_OaJLFM130_assertion description "[The primary syndromes (and genes) addressed here include multiple endocrine neoplasia types 1 and 2 (MEN1 and RET genes), Cowden syndrome (PTEN), hereditary pheochromocytoma/paraganglioma syndromes (multiple genes), and von Hippel-Lindau disease (VHL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP553195.RAfmt8v6cUQMwdMLu_CatH34tuORwubNLkqD27_OaJLFM130_provenance.