Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1077074.RA0XbPwK8K9C9kNTnkH306_pt4sXmcdKqwnVnaQlmUbEA130_assertion> ?p ?o ?g. }
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- NP1077074.RA0XbPwK8K9C9kNTnkH306_pt4sXmcdKqwnVnaQlmUbEA130_assertion type Assertion NP1077074.RA0XbPwK8K9C9kNTnkH306_pt4sXmcdKqwnVnaQlmUbEA130_head.
- NP1077074.RA0XbPwK8K9C9kNTnkH306_pt4sXmcdKqwnVnaQlmUbEA130_assertion description "[These results reveal that mutations in ADAM10 are a cause of RAK and that RAK is an independent clinical entity distinct from DDD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1077074.RA0XbPwK8K9C9kNTnkH306_pt4sXmcdKqwnVnaQlmUbEA130_provenance.
- NP1077074.RA0XbPwK8K9C9kNTnkH306_pt4sXmcdKqwnVnaQlmUbEA130_assertion evidence source_evidence_literature NP1077074.RA0XbPwK8K9C9kNTnkH306_pt4sXmcdKqwnVnaQlmUbEA130_provenance.
- NP1077074.RA0XbPwK8K9C9kNTnkH306_pt4sXmcdKqwnVnaQlmUbEA130_assertion SIO_000772 23666529 NP1077074.RA0XbPwK8K9C9kNTnkH306_pt4sXmcdKqwnVnaQlmUbEA130_provenance.
- NP1077074.RA0XbPwK8K9C9kNTnkH306_pt4sXmcdKqwnVnaQlmUbEA130_assertion wasDerivedFrom befree-2016 NP1077074.RA0XbPwK8K9C9kNTnkH306_pt4sXmcdKqwnVnaQlmUbEA130_provenance.
- NP1077074.RA0XbPwK8K9C9kNTnkH306_pt4sXmcdKqwnVnaQlmUbEA130_assertion wasGeneratedBy ECO_0000203 NP1077074.RA0XbPwK8K9C9kNTnkH306_pt4sXmcdKqwnVnaQlmUbEA130_provenance.