Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP276977.RAEB2-HkPLel0oD-S1iwwlvAOGo0pe6IyKtj-MxZy7RhY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP276977.RAEB2-HkPLel0oD-S1iwwlvAOGo0pe6IyKtj-MxZy7RhY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP276977.RAEB2-HkPLel0oD-S1iwwlvAOGo0pe6IyKtj-MxZy7RhY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP276977.RAEB2-HkPLel0oD-S1iwwlvAOGo0pe6IyKtj-MxZy7RhY130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP276977.RAEB2-HkPLel0oD-S1iwwlvAOGo0pe6IyKtj-MxZy7RhY130_provenance.