Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP943927.RADmV-LpoOTlalT9dhwc3jKWGRCn4lFii7JIt9d6yGwHM130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP943927.RADmV-LpoOTlalT9dhwc3jKWGRCn4lFii7JIt9d6yGwHM130_assertion type Assertion NP943927.RADmV-LpoOTlalT9dhwc3jKWGRCn4lFii7JIt9d6yGwHM130_head.
- NP943927.RADmV-LpoOTlalT9dhwc3jKWGRCn4lFii7JIt9d6yGwHM130_assertion wasGeneratedBy ECO_0000203 NP943927.RADmV-LpoOTlalT9dhwc3jKWGRCn4lFii7JIt9d6yGwHM130_provenance.
- NP943927.RADmV-LpoOTlalT9dhwc3jKWGRCn4lFii7JIt9d6yGwHM130_assertion wasDerivedFrom befree-2016 NP943927.RADmV-LpoOTlalT9dhwc3jKWGRCn4lFii7JIt9d6yGwHM130_provenance.
- NP943927.RADmV-LpoOTlalT9dhwc3jKWGRCn4lFii7JIt9d6yGwHM130_assertion SIO_000772 22140011 NP943927.RADmV-LpoOTlalT9dhwc3jKWGRCn4lFii7JIt9d6yGwHM130_provenance.
- NP943927.RADmV-LpoOTlalT9dhwc3jKWGRCn4lFii7JIt9d6yGwHM130_assertion evidence source_evidence_literature NP943927.RADmV-LpoOTlalT9dhwc3jKWGRCn4lFii7JIt9d6yGwHM130_provenance.
- NP943927.RADmV-LpoOTlalT9dhwc3jKWGRCn4lFii7JIt9d6yGwHM130_assertion description "[To date, 26 distinct SMC1A mutations have been identified in patients with Cornelia de Lange syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP943927.RADmV-LpoOTlalT9dhwc3jKWGRCn4lFii7JIt9d6yGwHM130_provenance.