Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP951883.RA-IKQbgNY4m1VStCobne6epQK9-BuekWAvxyrLcR5F7U130_assertion> ?p ?o ?g. }
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- NP951883.RA-IKQbgNY4m1VStCobne6epQK9-BuekWAvxyrLcR5F7U130_assertion type Assertion NP951883.RA-IKQbgNY4m1VStCobne6epQK9-BuekWAvxyrLcR5F7U130_head.
- NP951883.RA-IKQbgNY4m1VStCobne6epQK9-BuekWAvxyrLcR5F7U130_assertion description "[This finding and the previous findings of a 45% frequency of phenotypic color vision defects in patients with AMN may suggest that the ALD/AMN gene lies 5' to the red pigment gene and that the frequent phenotypic color vision anomalies owe their origin to deleted DNA that includes regulatory genes for color vision.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP951883.RA-IKQbgNY4m1VStCobne6epQK9-BuekWAvxyrLcR5F7U130_provenance.
- NP951883.RA-IKQbgNY4m1VStCobne6epQK9-BuekWAvxyrLcR5F7U130_assertion evidence source_evidence_literature NP951883.RA-IKQbgNY4m1VStCobne6epQK9-BuekWAvxyrLcR5F7U130_provenance.
- NP951883.RA-IKQbgNY4m1VStCobne6epQK9-BuekWAvxyrLcR5F7U130_assertion SIO_000772 2309698 NP951883.RA-IKQbgNY4m1VStCobne6epQK9-BuekWAvxyrLcR5F7U130_provenance.
- NP951883.RA-IKQbgNY4m1VStCobne6epQK9-BuekWAvxyrLcR5F7U130_assertion wasDerivedFrom befree-20150227 NP951883.RA-IKQbgNY4m1VStCobne6epQK9-BuekWAvxyrLcR5F7U130_provenance.
- NP951883.RA-IKQbgNY4m1VStCobne6epQK9-BuekWAvxyrLcR5F7U130_assertion wasGeneratedBy ECO_0000203 NP951883.RA-IKQbgNY4m1VStCobne6epQK9-BuekWAvxyrLcR5F7U130_provenance.