Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP361729.RAAtSxpj1mo-t1-DrQxnsUmswakIMDMXZ8B1XcPAMylUo130_assertion> ?p ?o ?g. }
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- NP361729.RAAtSxpj1mo-t1-DrQxnsUmswakIMDMXZ8B1XcPAMylUo130_assertion type Assertion NP361729.RAAtSxpj1mo-t1-DrQxnsUmswakIMDMXZ8B1XcPAMylUo130_head.
- NP361729.RAAtSxpj1mo-t1-DrQxnsUmswakIMDMXZ8B1XcPAMylUo130_assertion wasGeneratedBy ECO_0000203 NP361729.RAAtSxpj1mo-t1-DrQxnsUmswakIMDMXZ8B1XcPAMylUo130_provenance.
- NP361729.RAAtSxpj1mo-t1-DrQxnsUmswakIMDMXZ8B1XcPAMylUo130_assertion wasDerivedFrom befree-20150227 NP361729.RAAtSxpj1mo-t1-DrQxnsUmswakIMDMXZ8B1XcPAMylUo130_provenance.
- NP361729.RAAtSxpj1mo-t1-DrQxnsUmswakIMDMXZ8B1XcPAMylUo130_assertion SIO_000772 11260246 NP361729.RAAtSxpj1mo-t1-DrQxnsUmswakIMDMXZ8B1XcPAMylUo130_provenance.
- NP361729.RAAtSxpj1mo-t1-DrQxnsUmswakIMDMXZ8B1XcPAMylUo130_assertion evidence source_evidence_literature NP361729.RAAtSxpj1mo-t1-DrQxnsUmswakIMDMXZ8B1XcPAMylUo130_provenance.
- NP361729.RAAtSxpj1mo-t1-DrQxnsUmswakIMDMXZ8B1XcPAMylUo130_assertion description "[Similarly, a mutation in desmoglein 3 underlies the balding mouse phenotype, although no human mutations in desmoglein 3 have been identified to date.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP361729.RAAtSxpj1mo-t1-DrQxnsUmswakIMDMXZ8B1XcPAMylUo130_provenance.