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- NP835514.RAp0YKz5Gf6YEfBXk3NbmuP3AgnHkOfgEGoAJXp79EO5g130_assertion type Assertion NP835514.RAp0YKz5Gf6YEfBXk3NbmuP3AgnHkOfgEGoAJXp79EO5g130_head.
- NP835514.RAp0YKz5Gf6YEfBXk3NbmuP3AgnHkOfgEGoAJXp79EO5g130_assertion description "[ARX mutation testing should be undertaken in children aged less than 1 year with Ohtahara syndrome and a movement disorder, and in infants with unexplained neurodegeneration, progressive white matter loss, and cortical atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP835514.RAp0YKz5Gf6YEfBXk3NbmuP3AgnHkOfgEGoAJXp79EO5g130_provenance.
- NP835514.RAp0YKz5Gf6YEfBXk3NbmuP3AgnHkOfgEGoAJXp79EO5g130_assertion evidence source_evidence_literature NP835514.RAp0YKz5Gf6YEfBXk3NbmuP3AgnHkOfgEGoAJXp79EO5g130_provenance.
- NP835514.RAp0YKz5Gf6YEfBXk3NbmuP3AgnHkOfgEGoAJXp79EO5g130_assertion SIO_000772 19747203 NP835514.RAp0YKz5Gf6YEfBXk3NbmuP3AgnHkOfgEGoAJXp79EO5g130_provenance.
- NP835514.RAp0YKz5Gf6YEfBXk3NbmuP3AgnHkOfgEGoAJXp79EO5g130_assertion wasDerivedFrom befree-20150227 NP835514.RAp0YKz5Gf6YEfBXk3NbmuP3AgnHkOfgEGoAJXp79EO5g130_provenance.
- NP835514.RAp0YKz5Gf6YEfBXk3NbmuP3AgnHkOfgEGoAJXp79EO5g130_assertion wasGeneratedBy ECO_0000203 NP835514.RAp0YKz5Gf6YEfBXk3NbmuP3AgnHkOfgEGoAJXp79EO5g130_provenance.