Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP524860.RA-5J2uHqgFdC1uoxe4Le_mxN_6zIKunV4yWVhlHST2nM130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP524860.RA-5J2uHqgFdC1uoxe4Le_mxN_6zIKunV4yWVhlHST2nM130_assertion type Assertion NP524860.RA-5J2uHqgFdC1uoxe4Le_mxN_6zIKunV4yWVhlHST2nM130_head.
- NP524860.RA-5J2uHqgFdC1uoxe4Le_mxN_6zIKunV4yWVhlHST2nM130_assertion description "[Variability in clinical phenotype despite common chromosomal deletion in Smith-Magenis syndrome [del(17)(p11.2p11.2)].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP524860.RA-5J2uHqgFdC1uoxe4Le_mxN_6zIKunV4yWVhlHST2nM130_provenance.
- NP524860.RA-5J2uHqgFdC1uoxe4Le_mxN_6zIKunV4yWVhlHST2nM130_assertion evidence source_evidence_literature NP524860.RA-5J2uHqgFdC1uoxe4Le_mxN_6zIKunV4yWVhlHST2nM130_provenance.
- NP524860.RA-5J2uHqgFdC1uoxe4Le_mxN_6zIKunV4yWVhlHST2nM130_assertion SIO_000772 14614393 NP524860.RA-5J2uHqgFdC1uoxe4Le_mxN_6zIKunV4yWVhlHST2nM130_provenance.
- NP524860.RA-5J2uHqgFdC1uoxe4Le_mxN_6zIKunV4yWVhlHST2nM130_assertion wasDerivedFrom befree-20140225 NP524860.RA-5J2uHqgFdC1uoxe4Le_mxN_6zIKunV4yWVhlHST2nM130_provenance.
- NP524860.RA-5J2uHqgFdC1uoxe4Le_mxN_6zIKunV4yWVhlHST2nM130_assertion wasGeneratedBy ECO_0000203 NP524860.RA-5J2uHqgFdC1uoxe4Le_mxN_6zIKunV4yWVhlHST2nM130_provenance.