Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP51624.RABLtH-ROILi7nYy0Ij2L3MHesNCw8E86u_kyhe4rjYgo130_assertion> ?p ?o ?g. }
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- NP51624.RABLtH-ROILi7nYy0Ij2L3MHesNCw8E86u_kyhe4rjYgo130_assertion type Assertion NP51624.RABLtH-ROILi7nYy0Ij2L3MHesNCw8E86u_kyhe4rjYgo130_head.
- NP51624.RABLtH-ROILi7nYy0Ij2L3MHesNCw8E86u_kyhe4rjYgo130_assertion description "[We conclude that mutations of the GLUT4 coding sequence are very uncommon in this population of subjects with typical NIDDM. Determining whether the Ile383 GLUT4 variant present in 3 diabetic subjects contributes in any way to their disease will require further study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51624.RABLtH-ROILi7nYy0Ij2L3MHesNCw8E86u_kyhe4rjYgo130_provenance.
- NP51624.RABLtH-ROILi7nYy0Ij2L3MHesNCw8E86u_kyhe4rjYgo130_assertion evidence source_evidence_literature NP51624.RABLtH-ROILi7nYy0Ij2L3MHesNCw8E86u_kyhe4rjYgo130_provenance.
- NP51624.RABLtH-ROILi7nYy0Ij2L3MHesNCw8E86u_kyhe4rjYgo130_assertion SIO_000772 1756912 NP51624.RABLtH-ROILi7nYy0Ij2L3MHesNCw8E86u_kyhe4rjYgo130_provenance.
- NP51624.RABLtH-ROILi7nYy0Ij2L3MHesNCw8E86u_kyhe4rjYgo130_assertion wasDerivedFrom gad-20130706 NP51624.RABLtH-ROILi7nYy0Ij2L3MHesNCw8E86u_kyhe4rjYgo130_provenance.
- NP51624.RABLtH-ROILi7nYy0Ij2L3MHesNCw8E86u_kyhe4rjYgo130_assertion wasGeneratedBy ECO_0000203 NP51624.RABLtH-ROILi7nYy0Ij2L3MHesNCw8E86u_kyhe4rjYgo130_provenance.