Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP834896.RAcgfTOuRltC9D-EeQH71KadcP-lkgLtBXYa5965Ypzho130_assertion> ?p ?o ?g. }
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- NP834896.RAcgfTOuRltC9D-EeQH71KadcP-lkgLtBXYa5965Ypzho130_assertion type Assertion NP834896.RAcgfTOuRltC9D-EeQH71KadcP-lkgLtBXYa5965Ypzho130_head.
- NP834896.RAcgfTOuRltC9D-EeQH71KadcP-lkgLtBXYa5965Ypzho130_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." NP834896.RAcgfTOuRltC9D-EeQH71KadcP-lkgLtBXYa5965Ypzho130_provenance.
- NP834896.RAcgfTOuRltC9D-EeQH71KadcP-lkgLtBXYa5965Ypzho130_assertion evidence source_evidence_literature NP834896.RAcgfTOuRltC9D-EeQH71KadcP-lkgLtBXYa5965Ypzho130_provenance.
- NP834896.RAcgfTOuRltC9D-EeQH71KadcP-lkgLtBXYa5965Ypzho130_assertion SIO_000772 20736978 NP834896.RAcgfTOuRltC9D-EeQH71KadcP-lkgLtBXYa5965Ypzho130_provenance.
- NP834896.RAcgfTOuRltC9D-EeQH71KadcP-lkgLtBXYa5965Ypzho130_assertion wasDerivedFrom befree-2016 NP834896.RAcgfTOuRltC9D-EeQH71KadcP-lkgLtBXYa5965Ypzho130_provenance.
- NP834896.RAcgfTOuRltC9D-EeQH71KadcP-lkgLtBXYa5965Ypzho130_assertion wasGeneratedBy ECO_0000203 NP834896.RAcgfTOuRltC9D-EeQH71KadcP-lkgLtBXYa5965Ypzho130_provenance.