Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP87392.RA7ofbjf91sikR-fDe3L-WOzFJj5jU3ajUVlWNQCErds4#assertion> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- assertion wasGeneratedBy ECO_0000203 provenance.
- assertion wasDerivedFrom BEFREE provenance.
- assertion SIO_000772 1979048 provenance.
- assertion evidence source_evidence_literature provenance.
- assertion description "[Two independent familial STS deletions, one of which is associated with a phenotype of ichthyosis plus ocular albinism (XI/OA1) and the other with nystagmus plus Rud syndrome, lack some but not all of the normal S232 PFGE fragments.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.