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- NP734733.RAdeXNkixHvph2IGNE-_Rps2xUcFjqQKgMMTCxZF03dIc130_assertion type Assertion NP734733.RAdeXNkixHvph2IGNE-_Rps2xUcFjqQKgMMTCxZF03dIc130_head.
- NP734733.RAdeXNkixHvph2IGNE-_Rps2xUcFjqQKgMMTCxZF03dIc130_assertion description "[Disorders of respiratory control are a prominent feature of Rett syndrome (RTT), a severely debilitating condition caused by mutations in the gene encoding methyl-CpG-binding protein 2 (MECP2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP734733.RAdeXNkixHvph2IGNE-_Rps2xUcFjqQKgMMTCxZF03dIc130_provenance.
- NP734733.RAdeXNkixHvph2IGNE-_Rps2xUcFjqQKgMMTCxZF03dIc130_assertion evidence source_evidence_literature NP734733.RAdeXNkixHvph2IGNE-_Rps2xUcFjqQKgMMTCxZF03dIc130_provenance.
- NP734733.RAdeXNkixHvph2IGNE-_Rps2xUcFjqQKgMMTCxZF03dIc130_assertion SIO_000772 19394452 NP734733.RAdeXNkixHvph2IGNE-_Rps2xUcFjqQKgMMTCxZF03dIc130_provenance.
- NP734733.RAdeXNkixHvph2IGNE-_Rps2xUcFjqQKgMMTCxZF03dIc130_assertion wasDerivedFrom befree-2016 NP734733.RAdeXNkixHvph2IGNE-_Rps2xUcFjqQKgMMTCxZF03dIc130_provenance.
- NP734733.RAdeXNkixHvph2IGNE-_Rps2xUcFjqQKgMMTCxZF03dIc130_assertion wasGeneratedBy ECO_0000203 NP734733.RAdeXNkixHvph2IGNE-_Rps2xUcFjqQKgMMTCxZF03dIc130_provenance.