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- NP446224.RAUGEjSwr7BLtk_oB1Xx5hUJ8IVqS_BnOv5n2_jGxQduE130_assertion type Assertion NP446224.RAUGEjSwr7BLtk_oB1Xx5hUJ8IVqS_BnOv5n2_jGxQduE130_head.
- NP446224.RAUGEjSwr7BLtk_oB1Xx5hUJ8IVqS_BnOv5n2_jGxQduE130_assertion wasGeneratedBy ECO_0000203 NP446224.RAUGEjSwr7BLtk_oB1Xx5hUJ8IVqS_BnOv5n2_jGxQduE130_provenance.
- NP446224.RAUGEjSwr7BLtk_oB1Xx5hUJ8IVqS_BnOv5n2_jGxQduE130_assertion wasDerivedFrom befree-20140225 NP446224.RAUGEjSwr7BLtk_oB1Xx5hUJ8IVqS_BnOv5n2_jGxQduE130_provenance.
- NP446224.RAUGEjSwr7BLtk_oB1Xx5hUJ8IVqS_BnOv5n2_jGxQduE130_assertion SIO_000772 15466077 NP446224.RAUGEjSwr7BLtk_oB1Xx5hUJ8IVqS_BnOv5n2_jGxQduE130_provenance.
- NP446224.RAUGEjSwr7BLtk_oB1Xx5hUJ8IVqS_BnOv5n2_jGxQduE130_assertion evidence source_evidence_literature NP446224.RAUGEjSwr7BLtk_oB1Xx5hUJ8IVqS_BnOv5n2_jGxQduE130_provenance.
- NP446224.RAUGEjSwr7BLtk_oB1Xx5hUJ8IVqS_BnOv5n2_jGxQduE130_assertion description "[Deficiencies in fatty acid metabolism have been extensively studied in cases of SIDS, and by far the most well-investigated mutation is the A985G mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene, which is the most prevalent mutation causing MCAD deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP446224.RAUGEjSwr7BLtk_oB1Xx5hUJ8IVqS_BnOv5n2_jGxQduE130_provenance.