Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP789154.RAC7iBiSep2tDLI9R-dxVDai3oogEyNbnIJ7sJ4z6S7uQ130_assertion> ?p ?o ?g. }
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- NP789154.RAC7iBiSep2tDLI9R-dxVDai3oogEyNbnIJ7sJ4z6S7uQ130_assertion type Assertion NP789154.RAC7iBiSep2tDLI9R-dxVDai3oogEyNbnIJ7sJ4z6S7uQ130_head.
- NP789154.RAC7iBiSep2tDLI9R-dxVDai3oogEyNbnIJ7sJ4z6S7uQ130_assertion description "[MECP2 mutations have also been identified in individuals with a variety of clinical syndromes, including mild learning-disability in females, neonatal encephalopathy in males, and psychiatric disorders, autism and X-linked mental retardation in both males and females.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP789154.RAC7iBiSep2tDLI9R-dxVDai3oogEyNbnIJ7sJ4z6S7uQ130_provenance.
- NP789154.RAC7iBiSep2tDLI9R-dxVDai3oogEyNbnIJ7sJ4z6S7uQ130_assertion evidence source_evidence_literature NP789154.RAC7iBiSep2tDLI9R-dxVDai3oogEyNbnIJ7sJ4z6S7uQ130_provenance.
- NP789154.RAC7iBiSep2tDLI9R-dxVDai3oogEyNbnIJ7sJ4z6S7uQ130_assertion SIO_000772 16647848 NP789154.RAC7iBiSep2tDLI9R-dxVDai3oogEyNbnIJ7sJ4z6S7uQ130_provenance.
- NP789154.RAC7iBiSep2tDLI9R-dxVDai3oogEyNbnIJ7sJ4z6S7uQ130_assertion wasDerivedFrom befree-20140225 NP789154.RAC7iBiSep2tDLI9R-dxVDai3oogEyNbnIJ7sJ4z6S7uQ130_provenance.
- NP789154.RAC7iBiSep2tDLI9R-dxVDai3oogEyNbnIJ7sJ4z6S7uQ130_assertion wasGeneratedBy ECO_0000203 NP789154.RAC7iBiSep2tDLI9R-dxVDai3oogEyNbnIJ7sJ4z6S7uQ130_provenance.