Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1239178.RAlbvZnfKGFizfWsu_XUBiZTDrXnWJejNRVp0pJG9QlTU130_assertion> ?p ?o ?g. }
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- NP1239178.RAlbvZnfKGFizfWsu_XUBiZTDrXnWJejNRVp0pJG9QlTU130_assertion type Assertion NP1239178.RAlbvZnfKGFizfWsu_XUBiZTDrXnWJejNRVp0pJG9QlTU130_head.
- NP1239178.RAlbvZnfKGFizfWsu_XUBiZTDrXnWJejNRVp0pJG9QlTU130_assertion description "[The neurologic phenotype of WWOX mutation includes seizures, ataxia, developmental delay, and spasticity of variable severity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1239178.RAlbvZnfKGFizfWsu_XUBiZTDrXnWJejNRVp0pJG9QlTU130_provenance.
- NP1239178.RAlbvZnfKGFizfWsu_XUBiZTDrXnWJejNRVp0pJG9QlTU130_assertion evidence source_evidence_literature NP1239178.RAlbvZnfKGFizfWsu_XUBiZTDrXnWJejNRVp0pJG9QlTU130_provenance.
- NP1239178.RAlbvZnfKGFizfWsu_XUBiZTDrXnWJejNRVp0pJG9QlTU130_assertion SIO_000772 25416187 NP1239178.RAlbvZnfKGFizfWsu_XUBiZTDrXnWJejNRVp0pJG9QlTU130_provenance.
- NP1239178.RAlbvZnfKGFizfWsu_XUBiZTDrXnWJejNRVp0pJG9QlTU130_assertion wasDerivedFrom befree-2016 NP1239178.RAlbvZnfKGFizfWsu_XUBiZTDrXnWJejNRVp0pJG9QlTU130_provenance.
- NP1239178.RAlbvZnfKGFizfWsu_XUBiZTDrXnWJejNRVp0pJG9QlTU130_assertion wasGeneratedBy ECO_0000203 NP1239178.RAlbvZnfKGFizfWsu_XUBiZTDrXnWJejNRVp0pJG9QlTU130_provenance.