Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP293773.RAQkOEz0r5tObvLYUe6OCNOTD8xxFuqvBW_jAmjL6f5WA130_assertion> ?p ?o ?g. }
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- NP293773.RAQkOEz0r5tObvLYUe6OCNOTD8xxFuqvBW_jAmjL6f5WA130_assertion type Assertion NP293773.RAQkOEz0r5tObvLYUe6OCNOTD8xxFuqvBW_jAmjL6f5WA130_head.
- NP293773.RAQkOEz0r5tObvLYUe6OCNOTD8xxFuqvBW_jAmjL6f5WA130_assertion description "[Sequence analysis of candidate ACADs revealed heterozygosity for the common short-chain ACAD A625 variant allele and no mutations in ACAD-8 but a 100-bp deletion in short/branched-chain ACAD (SBCAD) cDNA from the patient.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP293773.RAQkOEz0r5tObvLYUe6OCNOTD8xxFuqvBW_jAmjL6f5WA130_provenance.
- NP293773.RAQkOEz0r5tObvLYUe6OCNOTD8xxFuqvBW_jAmjL6f5WA130_assertion evidence source_evidence_literature NP293773.RAQkOEz0r5tObvLYUe6OCNOTD8xxFuqvBW_jAmjL6f5WA130_provenance.
- NP293773.RAQkOEz0r5tObvLYUe6OCNOTD8xxFuqvBW_jAmjL6f5WA130_assertion SIO_000772 11013134 NP293773.RAQkOEz0r5tObvLYUe6OCNOTD8xxFuqvBW_jAmjL6f5WA130_provenance.
- NP293773.RAQkOEz0r5tObvLYUe6OCNOTD8xxFuqvBW_jAmjL6f5WA130_assertion wasDerivedFrom befree-20140225 NP293773.RAQkOEz0r5tObvLYUe6OCNOTD8xxFuqvBW_jAmjL6f5WA130_provenance.
- NP293773.RAQkOEz0r5tObvLYUe6OCNOTD8xxFuqvBW_jAmjL6f5WA130_assertion wasGeneratedBy ECO_0000203 NP293773.RAQkOEz0r5tObvLYUe6OCNOTD8xxFuqvBW_jAmjL6f5WA130_provenance.