Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP295853.RAIQhFI7rZ_kM-nt9FZF8y67Kc0Un6Q2hsOZMlIBQ2S0w130_assertion> ?p ?o ?g. }
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- NP295853.RAIQhFI7rZ_kM-nt9FZF8y67Kc0Un6Q2hsOZMlIBQ2S0w130_assertion type Assertion NP295853.RAIQhFI7rZ_kM-nt9FZF8y67Kc0Un6Q2hsOZMlIBQ2S0w130_head.
- NP295853.RAIQhFI7rZ_kM-nt9FZF8y67Kc0Un6Q2hsOZMlIBQ2S0w130_assertion description "[Mutations in the p63 gene have recently been delineated as the molecular basis for some cases of the ectrodactyly, ectodermal dysplasia and cleft lip/palate (EEC) syndrome, an autosomal dominant disorder (MIM 129900).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP295853.RAIQhFI7rZ_kM-nt9FZF8y67Kc0Un6Q2hsOZMlIBQ2S0w130_provenance.
- NP295853.RAIQhFI7rZ_kM-nt9FZF8y67Kc0Un6Q2hsOZMlIBQ2S0w130_assertion evidence source_evidence_literature NP295853.RAIQhFI7rZ_kM-nt9FZF8y67Kc0Un6Q2hsOZMlIBQ2S0w130_provenance.
- NP295853.RAIQhFI7rZ_kM-nt9FZF8y67Kc0Un6Q2hsOZMlIBQ2S0w130_assertion SIO_000772 11012604 NP295853.RAIQhFI7rZ_kM-nt9FZF8y67Kc0Un6Q2hsOZMlIBQ2S0w130_provenance.
- NP295853.RAIQhFI7rZ_kM-nt9FZF8y67Kc0Un6Q2hsOZMlIBQ2S0w130_assertion wasDerivedFrom befree-20140225 NP295853.RAIQhFI7rZ_kM-nt9FZF8y67Kc0Un6Q2hsOZMlIBQ2S0w130_provenance.
- NP295853.RAIQhFI7rZ_kM-nt9FZF8y67Kc0Un6Q2hsOZMlIBQ2S0w130_assertion wasGeneratedBy ECO_0000203 NP295853.RAIQhFI7rZ_kM-nt9FZF8y67Kc0Un6Q2hsOZMlIBQ2S0w130_provenance.