Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1001516.RAa_BM_UJJ20aoHUIWqvQTmcce057JROkbQhKLMMXJNMw130_assertion> ?p ?o ?g. }
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- NP1001516.RAa_BM_UJJ20aoHUIWqvQTmcce057JROkbQhKLMMXJNMw130_assertion type Assertion NP1001516.RAa_BM_UJJ20aoHUIWqvQTmcce057JROkbQhKLMMXJNMw130_head.
- NP1001516.RAa_BM_UJJ20aoHUIWqvQTmcce057JROkbQhKLMMXJNMw130_assertion wasGeneratedBy ECO_0000203 NP1001516.RAa_BM_UJJ20aoHUIWqvQTmcce057JROkbQhKLMMXJNMw130_provenance.
- NP1001516.RAa_BM_UJJ20aoHUIWqvQTmcce057JROkbQhKLMMXJNMw130_assertion wasDerivedFrom befree-2016 NP1001516.RAa_BM_UJJ20aoHUIWqvQTmcce057JROkbQhKLMMXJNMw130_provenance.
- NP1001516.RAa_BM_UJJ20aoHUIWqvQTmcce057JROkbQhKLMMXJNMw130_assertion SIO_000772 22846739 NP1001516.RAa_BM_UJJ20aoHUIWqvQTmcce057JROkbQhKLMMXJNMw130_provenance.
- NP1001516.RAa_BM_UJJ20aoHUIWqvQTmcce057JROkbQhKLMMXJNMw130_assertion evidence source_evidence_literature NP1001516.RAa_BM_UJJ20aoHUIWqvQTmcce057JROkbQhKLMMXJNMw130_provenance.
- NP1001516.RAa_BM_UJJ20aoHUIWqvQTmcce057JROkbQhKLMMXJNMw130_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." NP1001516.RAa_BM_UJJ20aoHUIWqvQTmcce057JROkbQhKLMMXJNMw130_provenance.