Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP799807.RA6nmyAPjfAiXqf0wcIH4JOUItP8kyifOGg7ymE7LX8Wo130_assertion> ?p ?o ?g. }
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- NP799807.RA6nmyAPjfAiXqf0wcIH4JOUItP8kyifOGg7ymE7LX8Wo130_assertion type Assertion NP799807.RA6nmyAPjfAiXqf0wcIH4JOUItP8kyifOGg7ymE7LX8Wo130_head.
- NP799807.RA6nmyAPjfAiXqf0wcIH4JOUItP8kyifOGg7ymE7LX8Wo130_assertion description "[Mutations in the p63 gene have been identified in five human disorders characterized by varying degrees of limb anomalies, ectodermal dysplasia, and facial clefts.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP799807.RA6nmyAPjfAiXqf0wcIH4JOUItP8kyifOGg7ymE7LX8Wo130_provenance.
- NP799807.RA6nmyAPjfAiXqf0wcIH4JOUItP8kyifOGg7ymE7LX8Wo130_assertion evidence source_evidence_literature NP799807.RA6nmyAPjfAiXqf0wcIH4JOUItP8kyifOGg7ymE7LX8Wo130_provenance.
- NP799807.RA6nmyAPjfAiXqf0wcIH4JOUItP8kyifOGg7ymE7LX8Wo130_assertion SIO_000772 16190990 NP799807.RA6nmyAPjfAiXqf0wcIH4JOUItP8kyifOGg7ymE7LX8Wo130_provenance.
- NP799807.RA6nmyAPjfAiXqf0wcIH4JOUItP8kyifOGg7ymE7LX8Wo130_assertion wasDerivedFrom befree-20150227 NP799807.RA6nmyAPjfAiXqf0wcIH4JOUItP8kyifOGg7ymE7LX8Wo130_provenance.
- NP799807.RA6nmyAPjfAiXqf0wcIH4JOUItP8kyifOGg7ymE7LX8Wo130_assertion wasGeneratedBy ECO_0000203 NP799807.RA6nmyAPjfAiXqf0wcIH4JOUItP8kyifOGg7ymE7LX8Wo130_provenance.