Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP537640.RA2MNWKJ9hCwPBj76uV0qiSN41eKy_KrE_wjJhbNvg6mc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP537640.RA2MNWKJ9hCwPBj76uV0qiSN41eKy_KrE_wjJhbNvg6mc130_assertion type Assertion NP537640.RA2MNWKJ9hCwPBj76uV0qiSN41eKy_KrE_wjJhbNvg6mc130_head.
- NP537640.RA2MNWKJ9hCwPBj76uV0qiSN41eKy_KrE_wjJhbNvg6mc130_assertion description "[In addition, the tail regions of A-type lamin variants that occur in Dunnigan-type familial partial lipodystrophy of (R482W) and Hutchison Gilford progeria syndrome (?607-656) bind to the SREBP1 polypeptide in vitro, and the corresponding FLAG-tagged full-length lamin variants co-immunoprecipitate the SREBP1 polypeptide in cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP537640.RA2MNWKJ9hCwPBj76uV0qiSN41eKy_KrE_wjJhbNvg6mc130_provenance.
- NP537640.RA2MNWKJ9hCwPBj76uV0qiSN41eKy_KrE_wjJhbNvg6mc130_assertion evidence source_evidence_literature NP537640.RA2MNWKJ9hCwPBj76uV0qiSN41eKy_KrE_wjJhbNvg6mc130_provenance.
- NP537640.RA2MNWKJ9hCwPBj76uV0qiSN41eKy_KrE_wjJhbNvg6mc130_assertion SIO_000772 21993218 NP537640.RA2MNWKJ9hCwPBj76uV0qiSN41eKy_KrE_wjJhbNvg6mc130_provenance.
- NP537640.RA2MNWKJ9hCwPBj76uV0qiSN41eKy_KrE_wjJhbNvg6mc130_assertion wasDerivedFrom befree-20150227 NP537640.RA2MNWKJ9hCwPBj76uV0qiSN41eKy_KrE_wjJhbNvg6mc130_provenance.
- NP537640.RA2MNWKJ9hCwPBj76uV0qiSN41eKy_KrE_wjJhbNvg6mc130_assertion wasGeneratedBy ECO_0000203 NP537640.RA2MNWKJ9hCwPBj76uV0qiSN41eKy_KrE_wjJhbNvg6mc130_provenance.