Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP208952.RADvfoJWK183EHNz3Y_vmAyUBmGLmZbd-7niia7TFIYFg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP208952.RADvfoJWK183EHNz3Y_vmAyUBmGLmZbd-7niia7TFIYFg130_assertion type Assertion NP208952.RADvfoJWK183EHNz3Y_vmAyUBmGLmZbd-7niia7TFIYFg130_head.
- NP208952.RADvfoJWK183EHNz3Y_vmAyUBmGLmZbd-7niia7TFIYFg130_assertion description "[Large deletions in Xq21 often are associated with contiguous gene syndromes consisting of X-linked deafness type 3 (DFN3), mental retardation (MRX), and choroideremia (CHM).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP208952.RADvfoJWK183EHNz3Y_vmAyUBmGLmZbd-7niia7TFIYFg130_provenance.
- NP208952.RADvfoJWK183EHNz3Y_vmAyUBmGLmZbd-7niia7TFIYFg130_assertion evidence source_evidence_literature NP208952.RADvfoJWK183EHNz3Y_vmAyUBmGLmZbd-7niia7TFIYFg130_provenance.
- NP208952.RADvfoJWK183EHNz3Y_vmAyUBmGLmZbd-7niia7TFIYFg130_assertion SIO_000772 10644430 NP208952.RADvfoJWK183EHNz3Y_vmAyUBmGLmZbd-7niia7TFIYFg130_provenance.
- NP208952.RADvfoJWK183EHNz3Y_vmAyUBmGLmZbd-7niia7TFIYFg130_assertion wasDerivedFrom befree-20140225 NP208952.RADvfoJWK183EHNz3Y_vmAyUBmGLmZbd-7niia7TFIYFg130_provenance.
- NP208952.RADvfoJWK183EHNz3Y_vmAyUBmGLmZbd-7niia7TFIYFg130_assertion wasGeneratedBy ECO_0000203 NP208952.RADvfoJWK183EHNz3Y_vmAyUBmGLmZbd-7niia7TFIYFg130_provenance.