Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP276977.RAEB2-HkPLel0oD-S1iwwlvAOGo0pe6IyKtj-MxZy7RhY130_assertion> ?p ?o ?g. }
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- NP276977.RAEB2-HkPLel0oD-S1iwwlvAOGo0pe6IyKtj-MxZy7RhY130_assertion type Assertion NP276977.RAEB2-HkPLel0oD-S1iwwlvAOGo0pe6IyKtj-MxZy7RhY130_head.
- NP276977.RAEB2-HkPLel0oD-S1iwwlvAOGo0pe6IyKtj-MxZy7RhY130_assertion description "[The classical form of severe spinal muscular atrophy (SMA type 1; Werdnig-Hoffmann disease) has a very consistent clinical phenotype that is well recognized by paediatricians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP276977.RAEB2-HkPLel0oD-S1iwwlvAOGo0pe6IyKtj-MxZy7RhY130_provenance.
- NP276977.RAEB2-HkPLel0oD-S1iwwlvAOGo0pe6IyKtj-MxZy7RhY130_assertion evidence source_evidence_literature NP276977.RAEB2-HkPLel0oD-S1iwwlvAOGo0pe6IyKtj-MxZy7RhY130_provenance.
- NP276977.RAEB2-HkPLel0oD-S1iwwlvAOGo0pe6IyKtj-MxZy7RhY130_assertion SIO_000772 10700538 NP276977.RAEB2-HkPLel0oD-S1iwwlvAOGo0pe6IyKtj-MxZy7RhY130_provenance.
- NP276977.RAEB2-HkPLel0oD-S1iwwlvAOGo0pe6IyKtj-MxZy7RhY130_assertion wasDerivedFrom befree-2016 NP276977.RAEB2-HkPLel0oD-S1iwwlvAOGo0pe6IyKtj-MxZy7RhY130_provenance.
- NP276977.RAEB2-HkPLel0oD-S1iwwlvAOGo0pe6IyKtj-MxZy7RhY130_assertion wasGeneratedBy ECO_0000203 NP276977.RAEB2-HkPLel0oD-S1iwwlvAOGo0pe6IyKtj-MxZy7RhY130_provenance.