Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1008085.RA_QN0gClKxqn6qgBxw2xfQTVm3d2PsPSPwLfM3kf63Vo130_assertion> ?p ?o ?g. }
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- NP1008085.RA_QN0gClKxqn6qgBxw2xfQTVm3d2PsPSPwLfM3kf63Vo130_assertion type Assertion NP1008085.RA_QN0gClKxqn6qgBxw2xfQTVm3d2PsPSPwLfM3kf63Vo130_head.
- NP1008085.RA_QN0gClKxqn6qgBxw2xfQTVm3d2PsPSPwLfM3kf63Vo130_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." NP1008085.RA_QN0gClKxqn6qgBxw2xfQTVm3d2PsPSPwLfM3kf63Vo130_provenance.
- NP1008085.RA_QN0gClKxqn6qgBxw2xfQTVm3d2PsPSPwLfM3kf63Vo130_assertion evidence source_evidence_literature NP1008085.RA_QN0gClKxqn6qgBxw2xfQTVm3d2PsPSPwLfM3kf63Vo130_provenance.
- NP1008085.RA_QN0gClKxqn6qgBxw2xfQTVm3d2PsPSPwLfM3kf63Vo130_assertion SIO_000772 21050479 NP1008085.RA_QN0gClKxqn6qgBxw2xfQTVm3d2PsPSPwLfM3kf63Vo130_provenance.
- NP1008085.RA_QN0gClKxqn6qgBxw2xfQTVm3d2PsPSPwLfM3kf63Vo130_assertion wasDerivedFrom befree-20150227 NP1008085.RA_QN0gClKxqn6qgBxw2xfQTVm3d2PsPSPwLfM3kf63Vo130_provenance.
- NP1008085.RA_QN0gClKxqn6qgBxw2xfQTVm3d2PsPSPwLfM3kf63Vo130_assertion wasGeneratedBy ECO_0000203 NP1008085.RA_QN0gClKxqn6qgBxw2xfQTVm3d2PsPSPwLfM3kf63Vo130_provenance.