Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP300492.RAAKT8CXB5Ei0gx3NPW92Dy4RtfK40E_VFxnlwdslO9rU130_assertion> ?p ?o ?g. }
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- NP300492.RAAKT8CXB5Ei0gx3NPW92Dy4RtfK40E_VFxnlwdslO9rU130_assertion type Assertion NP300492.RAAKT8CXB5Ei0gx3NPW92Dy4RtfK40E_VFxnlwdslO9rU130_head.
- NP300492.RAAKT8CXB5Ei0gx3NPW92Dy4RtfK40E_VFxnlwdslO9rU130_assertion wasGeneratedBy ECO_0000203 NP300492.RAAKT8CXB5Ei0gx3NPW92Dy4RtfK40E_VFxnlwdslO9rU130_provenance.
- NP300492.RAAKT8CXB5Ei0gx3NPW92Dy4RtfK40E_VFxnlwdslO9rU130_assertion wasDerivedFrom befree-20150227 NP300492.RAAKT8CXB5Ei0gx3NPW92Dy4RtfK40E_VFxnlwdslO9rU130_provenance.
- NP300492.RAAKT8CXB5Ei0gx3NPW92Dy4RtfK40E_VFxnlwdslO9rU130_assertion SIO_000772 8840534 NP300492.RAAKT8CXB5Ei0gx3NPW92Dy4RtfK40E_VFxnlwdslO9rU130_provenance.
- NP300492.RAAKT8CXB5Ei0gx3NPW92Dy4RtfK40E_VFxnlwdslO9rU130_assertion evidence source_evidence_literature NP300492.RAAKT8CXB5Ei0gx3NPW92Dy4RtfK40E_VFxnlwdslO9rU130_provenance.
- NP300492.RAAKT8CXB5Ei0gx3NPW92Dy4RtfK40E_VFxnlwdslO9rU130_assertion description "[The prevalence of the 985A-to-G mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene among Japanese patients with sudden infant death syndrome, Reye syndrome, unknown fatty acid oxidation disorders and severe motor and intellectual disabilities was studied using the PCR/Nco-I method for molecular diagnosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP300492.RAAKT8CXB5Ei0gx3NPW92Dy4RtfK40E_VFxnlwdslO9rU130_provenance.