Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP666432.RAHigDKq8oWgf3hrTYHXYvFqFwL-c7A_zTBYv1HdsfNZ0130_assertion> ?p ?o ?g. }
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- NP666432.RAHigDKq8oWgf3hrTYHXYvFqFwL-c7A_zTBYv1HdsfNZ0130_assertion type Assertion NP666432.RAHigDKq8oWgf3hrTYHXYvFqFwL-c7A_zTBYv1HdsfNZ0130_head.
- NP666432.RAHigDKq8oWgf3hrTYHXYvFqFwL-c7A_zTBYv1HdsfNZ0130_assertion description "[Wolcott-Rallison syndrome (WRS) is a rare autosomal recessive disease, characterized by neonatal/early-onset non-autoimmune insulin-requiring diabetes associated with skeletal dysplasia and growth retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP666432.RAHigDKq8oWgf3hrTYHXYvFqFwL-c7A_zTBYv1HdsfNZ0130_provenance.
- NP666432.RAHigDKq8oWgf3hrTYHXYvFqFwL-c7A_zTBYv1HdsfNZ0130_assertion evidence source_evidence_literature NP666432.RAHigDKq8oWgf3hrTYHXYvFqFwL-c7A_zTBYv1HdsfNZ0130_provenance.
- NP666432.RAHigDKq8oWgf3hrTYHXYvFqFwL-c7A_zTBYv1HdsfNZ0130_assertion SIO_000772 21050479 NP666432.RAHigDKq8oWgf3hrTYHXYvFqFwL-c7A_zTBYv1HdsfNZ0130_provenance.
- NP666432.RAHigDKq8oWgf3hrTYHXYvFqFwL-c7A_zTBYv1HdsfNZ0130_assertion wasDerivedFrom befree-20140225 NP666432.RAHigDKq8oWgf3hrTYHXYvFqFwL-c7A_zTBYv1HdsfNZ0130_provenance.
- NP666432.RAHigDKq8oWgf3hrTYHXYvFqFwL-c7A_zTBYv1HdsfNZ0130_assertion wasGeneratedBy ECO_0000203 NP666432.RAHigDKq8oWgf3hrTYHXYvFqFwL-c7A_zTBYv1HdsfNZ0130_provenance.