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- NP128495.RAq3y2lUz8DRx5BMEQgGvN831w9vfa4Rqi9ATNkFwYAR4130_assertion type Assertion NP128495.RAq3y2lUz8DRx5BMEQgGvN831w9vfa4Rqi9ATNkFwYAR4130_head.
- NP128495.RAq3y2lUz8DRx5BMEQgGvN831w9vfa4Rqi9ATNkFwYAR4130_assertion description "[All patients with POMT1 and POMT2 mutations had evidence of either structural or functional central nervous system involvement including four patients with mental retardation and a LGMD phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP128495.RAq3y2lUz8DRx5BMEQgGvN831w9vfa4Rqi9ATNkFwYAR4130_provenance.
- NP128495.RAq3y2lUz8DRx5BMEQgGvN831w9vfa4Rqi9ATNkFwYAR4130_assertion evidence source_evidence_literature NP128495.RAq3y2lUz8DRx5BMEQgGvN831w9vfa4Rqi9ATNkFwYAR4130_provenance.
- NP128495.RAq3y2lUz8DRx5BMEQgGvN831w9vfa4Rqi9ATNkFwYAR4130_assertion SIO_000772 17878207 NP128495.RAq3y2lUz8DRx5BMEQgGvN831w9vfa4Rqi9ATNkFwYAR4130_provenance.
- NP128495.RAq3y2lUz8DRx5BMEQgGvN831w9vfa4Rqi9ATNkFwYAR4130_assertion wasDerivedFrom gad-20150221 NP128495.RAq3y2lUz8DRx5BMEQgGvN831w9vfa4Rqi9ATNkFwYAR4130_provenance.
- NP128495.RAq3y2lUz8DRx5BMEQgGvN831w9vfa4Rqi9ATNkFwYAR4130_assertion wasGeneratedBy ECO_0000203 NP128495.RAq3y2lUz8DRx5BMEQgGvN831w9vfa4Rqi9ATNkFwYAR4130_provenance.