Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP658026.RA9Hs5ddVwUx4W1-GbNuFatKg13_C-YEcz8WDu-vKstcY130_assertion> ?p ?o ?g. }
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- NP658026.RA9Hs5ddVwUx4W1-GbNuFatKg13_C-YEcz8WDu-vKstcY130_assertion type Assertion NP658026.RA9Hs5ddVwUx4W1-GbNuFatKg13_C-YEcz8WDu-vKstcY130_head.
- NP658026.RA9Hs5ddVwUx4W1-GbNuFatKg13_C-YEcz8WDu-vKstcY130_assertion description "[Other vitreoretinal degenerations including a number of chondrodysplasias in addition to STL1 and STL2, enhanced S-cone syndrome caused by mutations in NR2E3, and autosomal dominant vitreoretinochoroidopathy caused by mutations in VMD2 are discussed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP658026.RA9Hs5ddVwUx4W1-GbNuFatKg13_C-YEcz8WDu-vKstcY130_provenance.
- NP658026.RA9Hs5ddVwUx4W1-GbNuFatKg13_C-YEcz8WDu-vKstcY130_assertion evidence source_evidence_literature NP658026.RA9Hs5ddVwUx4W1-GbNuFatKg13_C-YEcz8WDu-vKstcY130_provenance.
- NP658026.RA9Hs5ddVwUx4W1-GbNuFatKg13_C-YEcz8WDu-vKstcY130_assertion SIO_000772 18309337 NP658026.RA9Hs5ddVwUx4W1-GbNuFatKg13_C-YEcz8WDu-vKstcY130_provenance.
- NP658026.RA9Hs5ddVwUx4W1-GbNuFatKg13_C-YEcz8WDu-vKstcY130_assertion wasDerivedFrom befree-2016 NP658026.RA9Hs5ddVwUx4W1-GbNuFatKg13_C-YEcz8WDu-vKstcY130_provenance.
- NP658026.RA9Hs5ddVwUx4W1-GbNuFatKg13_C-YEcz8WDu-vKstcY130_assertion wasGeneratedBy ECO_0000203 NP658026.RA9Hs5ddVwUx4W1-GbNuFatKg13_C-YEcz8WDu-vKstcY130_provenance.