Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP473696.RAAasbQuhcK_PcD3w6zhFs6SrtjIn-mrAvpRgTkBOUBXY130_assertion> ?p ?o ?g. }
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- NP473696.RAAasbQuhcK_PcD3w6zhFs6SrtjIn-mrAvpRgTkBOUBXY130_assertion type Assertion NP473696.RAAasbQuhcK_PcD3w6zhFs6SrtjIn-mrAvpRgTkBOUBXY130_head.
- NP473696.RAAasbQuhcK_PcD3w6zhFs6SrtjIn-mrAvpRgTkBOUBXY130_assertion description "[Three rare autosomal recessive disorders share the combination of congenital muscular dystrophy and brain malformations including a neuronal migration defect: muscle-eye-brain disease (MEB), Walker-Warburg syndrome (WWS), and Fukuyama congenital muscular dystrophy (FCMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP473696.RAAasbQuhcK_PcD3w6zhFs6SrtjIn-mrAvpRgTkBOUBXY130_provenance.
- NP473696.RAAasbQuhcK_PcD3w6zhFs6SrtjIn-mrAvpRgTkBOUBXY130_assertion evidence source_evidence_literature NP473696.RAAasbQuhcK_PcD3w6zhFs6SrtjIn-mrAvpRgTkBOUBXY130_provenance.
- NP473696.RAAasbQuhcK_PcD3w6zhFs6SrtjIn-mrAvpRgTkBOUBXY130_assertion SIO_000772 11320179 NP473696.RAAasbQuhcK_PcD3w6zhFs6SrtjIn-mrAvpRgTkBOUBXY130_provenance.
- NP473696.RAAasbQuhcK_PcD3w6zhFs6SrtjIn-mrAvpRgTkBOUBXY130_assertion wasDerivedFrom befree-20140225 NP473696.RAAasbQuhcK_PcD3w6zhFs6SrtjIn-mrAvpRgTkBOUBXY130_provenance.
- NP473696.RAAasbQuhcK_PcD3w6zhFs6SrtjIn-mrAvpRgTkBOUBXY130_assertion wasGeneratedBy ECO_0000203 NP473696.RAAasbQuhcK_PcD3w6zhFs6SrtjIn-mrAvpRgTkBOUBXY130_provenance.