Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP742171.RAHarCmhfbaTZL5Mrt6k-flmH7eZwA9j5u2A_Oh2jlQAE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP742171.RAHarCmhfbaTZL5Mrt6k-flmH7eZwA9j5u2A_Oh2jlQAE130_assertion type Assertion NP742171.RAHarCmhfbaTZL5Mrt6k-flmH7eZwA9j5u2A_Oh2jlQAE130_head.
- NP742171.RAHarCmhfbaTZL5Mrt6k-flmH7eZwA9j5u2A_Oh2jlQAE130_assertion description "[Heterozygous mutations in the Berardinelli-Seip congenital lipodystrophy (BSCL2) gene have been associated with different clinical phenotypes including Silver syndrome/spastic paraplegia 17, distal hereditary motor neuropathy type V, and Charcot-Marie-Tooth disease type 2 (CMT2) with predominant hand involvement.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP742171.RAHarCmhfbaTZL5Mrt6k-flmH7eZwA9j5u2A_Oh2jlQAE130_provenance.
- NP742171.RAHarCmhfbaTZL5Mrt6k-flmH7eZwA9j5u2A_Oh2jlQAE130_assertion evidence source_evidence_literature NP742171.RAHarCmhfbaTZL5Mrt6k-flmH7eZwA9j5u2A_Oh2jlQAE130_provenance.
- NP742171.RAHarCmhfbaTZL5Mrt6k-flmH7eZwA9j5u2A_Oh2jlQAE130_assertion SIO_000772 20806400 NP742171.RAHarCmhfbaTZL5Mrt6k-flmH7eZwA9j5u2A_Oh2jlQAE130_provenance.
- NP742171.RAHarCmhfbaTZL5Mrt6k-flmH7eZwA9j5u2A_Oh2jlQAE130_assertion wasDerivedFrom befree-20140225 NP742171.RAHarCmhfbaTZL5Mrt6k-flmH7eZwA9j5u2A_Oh2jlQAE130_provenance.
- NP742171.RAHarCmhfbaTZL5Mrt6k-flmH7eZwA9j5u2A_Oh2jlQAE130_assertion wasGeneratedBy ECO_0000203 NP742171.RAHarCmhfbaTZL5Mrt6k-flmH7eZwA9j5u2A_Oh2jlQAE130_provenance.