Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP654048.RAc2pVkZhaPSCYHq0Gd_Y3i0AWPHfCmY93OMQLZ9TQWeI130_assertion> ?p ?o ?g. }
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- NP654048.RAc2pVkZhaPSCYHq0Gd_Y3i0AWPHfCmY93OMQLZ9TQWeI130_assertion type Assertion NP654048.RAc2pVkZhaPSCYHq0Gd_Y3i0AWPHfCmY93OMQLZ9TQWeI130_head.
- NP654048.RAc2pVkZhaPSCYHq0Gd_Y3i0AWPHfCmY93OMQLZ9TQWeI130_assertion description "[Deletions and inactivating mutations of FOXG1 have been associated with a Rett-like syndrome characterized by hypotonia, irritability, developmental delay, hand stereotypies, and deceleration of head growth.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP654048.RAc2pVkZhaPSCYHq0Gd_Y3i0AWPHfCmY93OMQLZ9TQWeI130_provenance.
- NP654048.RAc2pVkZhaPSCYHq0Gd_Y3i0AWPHfCmY93OMQLZ9TQWeI130_assertion evidence source_evidence_literature NP654048.RAc2pVkZhaPSCYHq0Gd_Y3i0AWPHfCmY93OMQLZ9TQWeI130_provenance.
- NP654048.RAc2pVkZhaPSCYHq0Gd_Y3i0AWPHfCmY93OMQLZ9TQWeI130_assertion SIO_000772 20736978 NP654048.RAc2pVkZhaPSCYHq0Gd_Y3i0AWPHfCmY93OMQLZ9TQWeI130_provenance.
- NP654048.RAc2pVkZhaPSCYHq0Gd_Y3i0AWPHfCmY93OMQLZ9TQWeI130_assertion wasDerivedFrom befree-20140225 NP654048.RAc2pVkZhaPSCYHq0Gd_Y3i0AWPHfCmY93OMQLZ9TQWeI130_provenance.
- NP654048.RAc2pVkZhaPSCYHq0Gd_Y3i0AWPHfCmY93OMQLZ9TQWeI130_assertion wasGeneratedBy ECO_0000203 NP654048.RAc2pVkZhaPSCYHq0Gd_Y3i0AWPHfCmY93OMQLZ9TQWeI130_provenance.