Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP979946.RAYSoaFtb2j_xoQLTN_79SQK0gYJISmewKhN3GzwT8WEM130_assertion> ?p ?o ?g. }
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- NP979946.RAYSoaFtb2j_xoQLTN_79SQK0gYJISmewKhN3GzwT8WEM130_assertion type Assertion NP979946.RAYSoaFtb2j_xoQLTN_79SQK0gYJISmewKhN3GzwT8WEM130_head.
- NP979946.RAYSoaFtb2j_xoQLTN_79SQK0gYJISmewKhN3GzwT8WEM130_assertion description "[Here, we report a case of diabetes in a 7-mo old child with compound heterozygous mutations in ABCC8 (SUR1[A30V] and SUR1[G296R]).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP979946.RAYSoaFtb2j_xoQLTN_79SQK0gYJISmewKhN3GzwT8WEM130_provenance.
- NP979946.RAYSoaFtb2j_xoQLTN_79SQK0gYJISmewKhN3GzwT8WEM130_assertion evidence source_evidence_literature NP979946.RAYSoaFtb2j_xoQLTN_79SQK0gYJISmewKhN3GzwT8WEM130_provenance.
- NP979946.RAYSoaFtb2j_xoQLTN_79SQK0gYJISmewKhN3GzwT8WEM130_assertion SIO_000772 22562119 NP979946.RAYSoaFtb2j_xoQLTN_79SQK0gYJISmewKhN3GzwT8WEM130_provenance.
- NP979946.RAYSoaFtb2j_xoQLTN_79SQK0gYJISmewKhN3GzwT8WEM130_assertion wasDerivedFrom befree-2016 NP979946.RAYSoaFtb2j_xoQLTN_79SQK0gYJISmewKhN3GzwT8WEM130_provenance.
- NP979946.RAYSoaFtb2j_xoQLTN_79SQK0gYJISmewKhN3GzwT8WEM130_assertion wasGeneratedBy ECO_0000203 NP979946.RAYSoaFtb2j_xoQLTN_79SQK0gYJISmewKhN3GzwT8WEM130_provenance.