Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP563502.RAvSbdbKTTQ5VcyOpNEOmUtOA9gyFLWMs2AtrE_7TzwzM130_assertion> ?p ?o ?g. }
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- NP563502.RAvSbdbKTTQ5VcyOpNEOmUtOA9gyFLWMs2AtrE_7TzwzM130_assertion type Assertion NP563502.RAvSbdbKTTQ5VcyOpNEOmUtOA9gyFLWMs2AtrE_7TzwzM130_head.
- NP563502.RAvSbdbKTTQ5VcyOpNEOmUtOA9gyFLWMs2AtrE_7TzwzM130_assertion wasGeneratedBy ECO_0000203 NP563502.RAvSbdbKTTQ5VcyOpNEOmUtOA9gyFLWMs2AtrE_7TzwzM130_provenance.
- NP563502.RAvSbdbKTTQ5VcyOpNEOmUtOA9gyFLWMs2AtrE_7TzwzM130_assertion wasDerivedFrom befree-20140225 NP563502.RAvSbdbKTTQ5VcyOpNEOmUtOA9gyFLWMs2AtrE_7TzwzM130_provenance.
- NP563502.RAvSbdbKTTQ5VcyOpNEOmUtOA9gyFLWMs2AtrE_7TzwzM130_assertion SIO_000772 1979048 NP563502.RAvSbdbKTTQ5VcyOpNEOmUtOA9gyFLWMs2AtrE_7TzwzM130_provenance.
- NP563502.RAvSbdbKTTQ5VcyOpNEOmUtOA9gyFLWMs2AtrE_7TzwzM130_assertion evidence source_evidence_literature NP563502.RAvSbdbKTTQ5VcyOpNEOmUtOA9gyFLWMs2AtrE_7TzwzM130_provenance.
- NP563502.RAvSbdbKTTQ5VcyOpNEOmUtOA9gyFLWMs2AtrE_7TzwzM130_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." NP563502.RAvSbdbKTTQ5VcyOpNEOmUtOA9gyFLWMs2AtrE_7TzwzM130_provenance.