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- NP552018.RAtZX8R-tsBTLCZxkflSsrhWzSwJ0UsimqeF8FJFrdDjk130_assertion type Assertion NP552018.RAtZX8R-tsBTLCZxkflSsrhWzSwJ0UsimqeF8FJFrdDjk130_head.
- NP552018.RAtZX8R-tsBTLCZxkflSsrhWzSwJ0UsimqeF8FJFrdDjk130_assertion description "[Although the phenotype of CDKL5 mutation is similar to Rett syndrome caused by MECP2 mutation, the former is characterized by early-onset seizures and association with West syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP552018.RAtZX8R-tsBTLCZxkflSsrhWzSwJ0UsimqeF8FJFrdDjk130_provenance.
- NP552018.RAtZX8R-tsBTLCZxkflSsrhWzSwJ0UsimqeF8FJFrdDjk130_assertion evidence source_evidence_literature NP552018.RAtZX8R-tsBTLCZxkflSsrhWzSwJ0UsimqeF8FJFrdDjk130_provenance.
- NP552018.RAtZX8R-tsBTLCZxkflSsrhWzSwJ0UsimqeF8FJFrdDjk130_assertion SIO_000772 16806828 NP552018.RAtZX8R-tsBTLCZxkflSsrhWzSwJ0UsimqeF8FJFrdDjk130_provenance.
- NP552018.RAtZX8R-tsBTLCZxkflSsrhWzSwJ0UsimqeF8FJFrdDjk130_assertion wasDerivedFrom befree-20150227 NP552018.RAtZX8R-tsBTLCZxkflSsrhWzSwJ0UsimqeF8FJFrdDjk130_provenance.
- NP552018.RAtZX8R-tsBTLCZxkflSsrhWzSwJ0UsimqeF8FJFrdDjk130_assertion wasGeneratedBy ECO_0000203 NP552018.RAtZX8R-tsBTLCZxkflSsrhWzSwJ0UsimqeF8FJFrdDjk130_provenance.