Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP797475.RACd98UYnr4mn6Irc7kIT6SVtM4N7_VTsp7WbiUP9CphU130_assertion> ?p ?o ?g. }
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- NP797475.RACd98UYnr4mn6Irc7kIT6SVtM4N7_VTsp7WbiUP9CphU130_assertion type Assertion NP797475.RACd98UYnr4mn6Irc7kIT6SVtM4N7_VTsp7WbiUP9CphU130_head.
- NP797475.RACd98UYnr4mn6Irc7kIT6SVtM4N7_VTsp7WbiUP9CphU130_assertion wasGeneratedBy ECO_0000203 NP797475.RACd98UYnr4mn6Irc7kIT6SVtM4N7_VTsp7WbiUP9CphU130_provenance.
- NP797475.RACd98UYnr4mn6Irc7kIT6SVtM4N7_VTsp7WbiUP9CphU130_assertion wasDerivedFrom befree-20150227 NP797475.RACd98UYnr4mn6Irc7kIT6SVtM4N7_VTsp7WbiUP9CphU130_provenance.
- NP797475.RACd98UYnr4mn6Irc7kIT6SVtM4N7_VTsp7WbiUP9CphU130_assertion SIO_000772 21734245 NP797475.RACd98UYnr4mn6Irc7kIT6SVtM4N7_VTsp7WbiUP9CphU130_provenance.
- NP797475.RACd98UYnr4mn6Irc7kIT6SVtM4N7_VTsp7WbiUP9CphU130_assertion evidence source_evidence_literature NP797475.RACd98UYnr4mn6Irc7kIT6SVtM4N7_VTsp7WbiUP9CphU130_provenance.
- NP797475.RACd98UYnr4mn6Irc7kIT6SVtM4N7_VTsp7WbiUP9CphU130_assertion description "[Hypomorphic mutations in the X-linked NEMO gene and hypermorphic mutations in the autosomal IKBA gene cause X-linked recessive and autosomal dominant anhidrotic ectodermal dysplasia with immunodeficiency (EDA-ID) syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP797475.RACd98UYnr4mn6Irc7kIT6SVtM4N7_VTsp7WbiUP9CphU130_provenance.