Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1242287.RA6SirmDEX3dYV4SA84EBCJwk_e-WSzBDoKzPwghT0iic130_assertion> ?p ?o ?g. }
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- NP1242287.RA6SirmDEX3dYV4SA84EBCJwk_e-WSzBDoKzPwghT0iic130_assertion type Assertion NP1242287.RA6SirmDEX3dYV4SA84EBCJwk_e-WSzBDoKzPwghT0iic130_head.
- NP1242287.RA6SirmDEX3dYV4SA84EBCJwk_e-WSzBDoKzPwghT0iic130_assertion description "[The phenotypic spectrum of ATP1A3-related neurological disorders continues to expand beyond the distinct yet overlapping phenotypes in patients with AHC, RDP, and CAPOS syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1242287.RA6SirmDEX3dYV4SA84EBCJwk_e-WSzBDoKzPwghT0iic130_provenance.
- NP1242287.RA6SirmDEX3dYV4SA84EBCJwk_e-WSzBDoKzPwghT0iic130_assertion evidence source_evidence_literature NP1242287.RA6SirmDEX3dYV4SA84EBCJwk_e-WSzBDoKzPwghT0iic130_provenance.
- NP1242287.RA6SirmDEX3dYV4SA84EBCJwk_e-WSzBDoKzPwghT0iic130_assertion SIO_000772 25447930 NP1242287.RA6SirmDEX3dYV4SA84EBCJwk_e-WSzBDoKzPwghT0iic130_provenance.
- NP1242287.RA6SirmDEX3dYV4SA84EBCJwk_e-WSzBDoKzPwghT0iic130_assertion wasDerivedFrom befree-2016 NP1242287.RA6SirmDEX3dYV4SA84EBCJwk_e-WSzBDoKzPwghT0iic130_provenance.
- NP1242287.RA6SirmDEX3dYV4SA84EBCJwk_e-WSzBDoKzPwghT0iic130_assertion wasGeneratedBy ECO_0000203 NP1242287.RA6SirmDEX3dYV4SA84EBCJwk_e-WSzBDoKzPwghT0iic130_provenance.