Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP380764.RA3nPkrzi11ZvIht59X4azpbx-guz6sGctTYyKhYHkd8c130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP380764.RA3nPkrzi11ZvIht59X4azpbx-guz6sGctTYyKhYHkd8c130_assertion type Assertion NP380764.RA3nPkrzi11ZvIht59X4azpbx-guz6sGctTYyKhYHkd8c130_head.
- NP380764.RA3nPkrzi11ZvIht59X4azpbx-guz6sGctTYyKhYHkd8c130_assertion description "[This AIR pattern suggested a K(ATP) channel defect because it resembled that seen in children with recessive hyperinsulinism due to two common SUR1 mutations, g3992-9a and delPhe1388.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP380764.RA3nPkrzi11ZvIht59X4azpbx-guz6sGctTYyKhYHkd8c130_provenance.
- NP380764.RA3nPkrzi11ZvIht59X4azpbx-guz6sGctTYyKhYHkd8c130_assertion evidence source_evidence_literature NP380764.RA3nPkrzi11ZvIht59X4azpbx-guz6sGctTYyKhYHkd8c130_provenance.
- NP380764.RA3nPkrzi11ZvIht59X4azpbx-guz6sGctTYyKhYHkd8c130_assertion SIO_000772 12941782 NP380764.RA3nPkrzi11ZvIht59X4azpbx-guz6sGctTYyKhYHkd8c130_provenance.
- NP380764.RA3nPkrzi11ZvIht59X4azpbx-guz6sGctTYyKhYHkd8c130_assertion wasDerivedFrom befree-20140225 NP380764.RA3nPkrzi11ZvIht59X4azpbx-guz6sGctTYyKhYHkd8c130_provenance.
- NP380764.RA3nPkrzi11ZvIht59X4azpbx-guz6sGctTYyKhYHkd8c130_assertion wasGeneratedBy ECO_0000203 NP380764.RA3nPkrzi11ZvIht59X4azpbx-guz6sGctTYyKhYHkd8c130_provenance.