Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP916898.RAk7rMegbV9ty-UVxQa3faRf_yYe5WyDSIdmvMw7mwqF0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP916898.RAk7rMegbV9ty-UVxQa3faRf_yYe5WyDSIdmvMw7mwqF0130_assertion type Assertion NP916898.RAk7rMegbV9ty-UVxQa3faRf_yYe5WyDSIdmvMw7mwqF0130_head.
- NP916898.RAk7rMegbV9ty-UVxQa3faRf_yYe5WyDSIdmvMw7mwqF0130_assertion description "[This is the second reported case of the modifying effects of FLG null alleles on XLI and strengthens the hypothesis that filaggrin defects can synergize with STS deficiency to exacerbate the ichthyosis phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP916898.RAk7rMegbV9ty-UVxQa3faRf_yYe5WyDSIdmvMw7mwqF0130_provenance.
- NP916898.RAk7rMegbV9ty-UVxQa3faRf_yYe5WyDSIdmvMw7mwqF0130_assertion evidence source_evidence_literature NP916898.RAk7rMegbV9ty-UVxQa3faRf_yYe5WyDSIdmvMw7mwqF0130_provenance.
- NP916898.RAk7rMegbV9ty-UVxQa3faRf_yYe5WyDSIdmvMw7mwqF0130_assertion SIO_000772 21945601 NP916898.RAk7rMegbV9ty-UVxQa3faRf_yYe5WyDSIdmvMw7mwqF0130_provenance.
- NP916898.RAk7rMegbV9ty-UVxQa3faRf_yYe5WyDSIdmvMw7mwqF0130_assertion wasDerivedFrom befree-20140225 NP916898.RAk7rMegbV9ty-UVxQa3faRf_yYe5WyDSIdmvMw7mwqF0130_provenance.
- NP916898.RAk7rMegbV9ty-UVxQa3faRf_yYe5WyDSIdmvMw7mwqF0130_assertion wasGeneratedBy ECO_0000203 NP916898.RAk7rMegbV9ty-UVxQa3faRf_yYe5WyDSIdmvMw7mwqF0130_provenance.