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- NP789994.RADLy_NIACM-OPlYS85EzKIsifUc85ZRTQNAS3OYl2kEU130_assertion type Assertion NP789994.RADLy_NIACM-OPlYS85EzKIsifUc85ZRTQNAS3OYl2kEU130_head.
- NP789994.RADLy_NIACM-OPlYS85EzKIsifUc85ZRTQNAS3OYl2kEU130_assertion description "[Allelic mutations in each of these genes can result in a wide spectrum of clinical conditions, ranging from severe congenital onset with associated structural brain malformations (Walker Warburg syndrome; muscle-eye-brain disease; Fukuyama muscular dystrophy; congenital muscular dystrophy type 1D) to a relatively milder congenital variant with no brain involvement (congenital muscular dystrophy type 1C), and to limb-girdle muscular dystrophy (LGMD) type 2 variants with onset in childhood or adult life (LGMD2I, LGMD2L, and LGMD2N).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP789994.RADLy_NIACM-OPlYS85EzKIsifUc85ZRTQNAS3OYl2kEU130_provenance.
- NP789994.RADLy_NIACM-OPlYS85EzKIsifUc85ZRTQNAS3OYl2kEU130_assertion evidence source_evidence_literature NP789994.RADLy_NIACM-OPlYS85EzKIsifUc85ZRTQNAS3OYl2kEU130_provenance.
- NP789994.RADLy_NIACM-OPlYS85EzKIsifUc85ZRTQNAS3OYl2kEU130_assertion SIO_000772 19019316 NP789994.RADLy_NIACM-OPlYS85EzKIsifUc85ZRTQNAS3OYl2kEU130_provenance.
- NP789994.RADLy_NIACM-OPlYS85EzKIsifUc85ZRTQNAS3OYl2kEU130_assertion wasDerivedFrom befree-20140225 NP789994.RADLy_NIACM-OPlYS85EzKIsifUc85ZRTQNAS3OYl2kEU130_provenance.
- NP789994.RADLy_NIACM-OPlYS85EzKIsifUc85ZRTQNAS3OYl2kEU130_assertion wasGeneratedBy ECO_0000203 NP789994.RADLy_NIACM-OPlYS85EzKIsifUc85ZRTQNAS3OYl2kEU130_provenance.