Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1012259.RAy8Q4GbdvvnRYmp_uXYWrY6oIuR9U3Owst1nzeOzfAkU130_assertion> ?p ?o ?g. }
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- NP1012259.RAy8Q4GbdvvnRYmp_uXYWrY6oIuR9U3Owst1nzeOzfAkU130_assertion type Assertion NP1012259.RAy8Q4GbdvvnRYmp_uXYWrY6oIuR9U3Owst1nzeOzfAkU130_head.
- NP1012259.RAy8Q4GbdvvnRYmp_uXYWrY6oIuR9U3Owst1nzeOzfAkU130_assertion description "[The skin disease erythrokeratoderma variabilis (EKV) has been shown to be associated with mutations in GJB3 and GJB4 encoding connexin (Cx)31 and Cx30.3, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1012259.RAy8Q4GbdvvnRYmp_uXYWrY6oIuR9U3Owst1nzeOzfAkU130_provenance.
- NP1012259.RAy8Q4GbdvvnRYmp_uXYWrY6oIuR9U3Owst1nzeOzfAkU130_assertion evidence source_evidence_literature NP1012259.RAy8Q4GbdvvnRYmp_uXYWrY6oIuR9U3Owst1nzeOzfAkU130_provenance.
- NP1012259.RAy8Q4GbdvvnRYmp_uXYWrY6oIuR9U3Owst1nzeOzfAkU130_assertion SIO_000772 16297190 NP1012259.RAy8Q4GbdvvnRYmp_uXYWrY6oIuR9U3Owst1nzeOzfAkU130_provenance.
- NP1012259.RAy8Q4GbdvvnRYmp_uXYWrY6oIuR9U3Owst1nzeOzfAkU130_assertion wasDerivedFrom befree-20150227 NP1012259.RAy8Q4GbdvvnRYmp_uXYWrY6oIuR9U3Owst1nzeOzfAkU130_provenance.
- NP1012259.RAy8Q4GbdvvnRYmp_uXYWrY6oIuR9U3Owst1nzeOzfAkU130_assertion wasGeneratedBy ECO_0000203 NP1012259.RAy8Q4GbdvvnRYmp_uXYWrY6oIuR9U3Owst1nzeOzfAkU130_provenance.