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- NP835753.RAQjV8S-8yZVwRNuwTdxya0CK9J_zmkdo7gJIc2rK1sbo130_assertion type Assertion NP835753.RAQjV8S-8yZVwRNuwTdxya0CK9J_zmkdo7gJIc2rK1sbo130_head.
- NP835753.RAQjV8S-8yZVwRNuwTdxya0CK9J_zmkdo7gJIc2rK1sbo130_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." NP835753.RAQjV8S-8yZVwRNuwTdxya0CK9J_zmkdo7gJIc2rK1sbo130_provenance.
- NP835753.RAQjV8S-8yZVwRNuwTdxya0CK9J_zmkdo7gJIc2rK1sbo130_assertion evidence source_evidence_literature NP835753.RAQjV8S-8yZVwRNuwTdxya0CK9J_zmkdo7gJIc2rK1sbo130_provenance.
- NP835753.RAQjV8S-8yZVwRNuwTdxya0CK9J_zmkdo7gJIc2rK1sbo130_assertion SIO_000772 11320179 NP835753.RAQjV8S-8yZVwRNuwTdxya0CK9J_zmkdo7gJIc2rK1sbo130_provenance.
- NP835753.RAQjV8S-8yZVwRNuwTdxya0CK9J_zmkdo7gJIc2rK1sbo130_assertion wasDerivedFrom befree-20140225 NP835753.RAQjV8S-8yZVwRNuwTdxya0CK9J_zmkdo7gJIc2rK1sbo130_provenance.
- NP835753.RAQjV8S-8yZVwRNuwTdxya0CK9J_zmkdo7gJIc2rK1sbo130_assertion wasGeneratedBy ECO_0000203 NP835753.RAQjV8S-8yZVwRNuwTdxya0CK9J_zmkdo7gJIc2rK1sbo130_provenance.