Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP806518.RA9E80sAXoayvM_cubLiBGUoa60fm5VX6eROCe5DOixZU130_assertion> ?p ?o ?g. }
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- NP806518.RA9E80sAXoayvM_cubLiBGUoa60fm5VX6eROCe5DOixZU130_assertion type Assertion NP806518.RA9E80sAXoayvM_cubLiBGUoa60fm5VX6eROCe5DOixZU130_head.
- NP806518.RA9E80sAXoayvM_cubLiBGUoa60fm5VX6eROCe5DOixZU130_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." NP806518.RA9E80sAXoayvM_cubLiBGUoa60fm5VX6eROCe5DOixZU130_provenance.
- NP806518.RA9E80sAXoayvM_cubLiBGUoa60fm5VX6eROCe5DOixZU130_assertion evidence source_evidence_literature NP806518.RA9E80sAXoayvM_cubLiBGUoa60fm5VX6eROCe5DOixZU130_provenance.
- NP806518.RA9E80sAXoayvM_cubLiBGUoa60fm5VX6eROCe5DOixZU130_assertion SIO_000772 11320179 NP806518.RA9E80sAXoayvM_cubLiBGUoa60fm5VX6eROCe5DOixZU130_provenance.
- NP806518.RA9E80sAXoayvM_cubLiBGUoa60fm5VX6eROCe5DOixZU130_assertion wasDerivedFrom befree-20140225 NP806518.RA9E80sAXoayvM_cubLiBGUoa60fm5VX6eROCe5DOixZU130_provenance.
- NP806518.RA9E80sAXoayvM_cubLiBGUoa60fm5VX6eROCe5DOixZU130_assertion wasGeneratedBy ECO_0000203 NP806518.RA9E80sAXoayvM_cubLiBGUoa60fm5VX6eROCe5DOixZU130_provenance.