Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP343256.RA3MIFUVMKnzX4KEO9FDQqr42d0W-TFD75dZsrJO2aJus130_assertion> ?p ?o ?g. }
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- NP343256.RA3MIFUVMKnzX4KEO9FDQqr42d0W-TFD75dZsrJO2aJus130_assertion type Assertion NP343256.RA3MIFUVMKnzX4KEO9FDQqr42d0W-TFD75dZsrJO2aJus130_head.
- NP343256.RA3MIFUVMKnzX4KEO9FDQqr42d0W-TFD75dZsrJO2aJus130_assertion description "[Thus, our results confirm that mutations of SLC2A2 are the basic defect in patients with FBS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP343256.RA3MIFUVMKnzX4KEO9FDQqr42d0W-TFD75dZsrJO2aJus130_provenance.
- NP343256.RA3MIFUVMKnzX4KEO9FDQqr42d0W-TFD75dZsrJO2aJus130_assertion evidence source_evidence_literature NP343256.RA3MIFUVMKnzX4KEO9FDQqr42d0W-TFD75dZsrJO2aJus130_provenance.
- NP343256.RA3MIFUVMKnzX4KEO9FDQqr42d0W-TFD75dZsrJO2aJus130_assertion SIO_000772 11810292 NP343256.RA3MIFUVMKnzX4KEO9FDQqr42d0W-TFD75dZsrJO2aJus130_provenance.
- NP343256.RA3MIFUVMKnzX4KEO9FDQqr42d0W-TFD75dZsrJO2aJus130_assertion wasDerivedFrom befree-2016 NP343256.RA3MIFUVMKnzX4KEO9FDQqr42d0W-TFD75dZsrJO2aJus130_provenance.
- NP343256.RA3MIFUVMKnzX4KEO9FDQqr42d0W-TFD75dZsrJO2aJus130_assertion wasGeneratedBy ECO_0000203 NP343256.RA3MIFUVMKnzX4KEO9FDQqr42d0W-TFD75dZsrJO2aJus130_provenance.