Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP209323.RAEITlgbuahl-FiAeOZmLeVID0SN4a4JIxWHPEvFps0Wc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP209323.RAEITlgbuahl-FiAeOZmLeVID0SN4a4JIxWHPEvFps0Wc130_assertion type Assertion NP209323.RAEITlgbuahl-FiAeOZmLeVID0SN4a4JIxWHPEvFps0Wc130_head.
- NP209323.RAEITlgbuahl-FiAeOZmLeVID0SN4a4JIxWHPEvFps0Wc130_assertion wasGeneratedBy ECO_0000203 NP209323.RAEITlgbuahl-FiAeOZmLeVID0SN4a4JIxWHPEvFps0Wc130_provenance.
- NP209323.RAEITlgbuahl-FiAeOZmLeVID0SN4a4JIxWHPEvFps0Wc130_assertion wasDerivedFrom befree-20140225 NP209323.RAEITlgbuahl-FiAeOZmLeVID0SN4a4JIxWHPEvFps0Wc130_provenance.
- NP209323.RAEITlgbuahl-FiAeOZmLeVID0SN4a4JIxWHPEvFps0Wc130_assertion SIO_000772 7682883 NP209323.RAEITlgbuahl-FiAeOZmLeVID0SN4a4JIxWHPEvFps0Wc130_provenance.
- NP209323.RAEITlgbuahl-FiAeOZmLeVID0SN4a4JIxWHPEvFps0Wc130_assertion evidence source_evidence_literature NP209323.RAEITlgbuahl-FiAeOZmLeVID0SN4a4JIxWHPEvFps0Wc130_provenance.
- NP209323.RAEITlgbuahl-FiAeOZmLeVID0SN4a4JIxWHPEvFps0Wc130_assertion description "[A mutation (Met-->Arg) in the type I keratin (K14) gene responsible for autosomal dominant epidermolysis bullosa simplex.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP209323.RAEITlgbuahl-FiAeOZmLeVID0SN4a4JIxWHPEvFps0Wc130_provenance.