Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP184015.RApp9XuTowhWxv52WsyrdN4sLBrF7Cfuw0S7r2QIez1wI130_assertion> ?p ?o ?g. }
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- NP184015.RApp9XuTowhWxv52WsyrdN4sLBrF7Cfuw0S7r2QIez1wI130_assertion type Assertion NP184015.RApp9XuTowhWxv52WsyrdN4sLBrF7Cfuw0S7r2QIez1wI130_head.
- NP184015.RApp9XuTowhWxv52WsyrdN4sLBrF7Cfuw0S7r2QIez1wI130_assertion wasGeneratedBy ECO_0000203 NP184015.RApp9XuTowhWxv52WsyrdN4sLBrF7Cfuw0S7r2QIez1wI130_provenance.
- NP184015.RApp9XuTowhWxv52WsyrdN4sLBrF7Cfuw0S7r2QIez1wI130_assertion wasDerivedFrom lhgdn-20090331 NP184015.RApp9XuTowhWxv52WsyrdN4sLBrF7Cfuw0S7r2QIez1wI130_provenance.
- NP184015.RApp9XuTowhWxv52WsyrdN4sLBrF7Cfuw0S7r2QIez1wI130_assertion SIO_000772 15580558 NP184015.RApp9XuTowhWxv52WsyrdN4sLBrF7Cfuw0S7r2QIez1wI130_provenance.
- NP184015.RApp9XuTowhWxv52WsyrdN4sLBrF7Cfuw0S7r2QIez1wI130_assertion evidence source_evidence_literature NP184015.RApp9XuTowhWxv52WsyrdN4sLBrF7Cfuw0S7r2QIez1wI130_provenance.
- NP184015.RApp9XuTowhWxv52WsyrdN4sLBrF7Cfuw0S7r2QIez1wI130_assertion description "[KCNJ11 mutations are a common cause of permanent neonatal diabetes mellitus either in isolation or associated with developmental delay]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184015.RApp9XuTowhWxv52WsyrdN4sLBrF7Cfuw0S7r2QIez1wI130_provenance.