Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1235327.RACNgG7f8CuCfRXR_S24tWRLdH_WjltqqNFIOlXsbnrFA130_assertion> ?p ?o ?g. }
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- NP1235327.RACNgG7f8CuCfRXR_S24tWRLdH_WjltqqNFIOlXsbnrFA130_assertion type Assertion NP1235327.RACNgG7f8CuCfRXR_S24tWRLdH_WjltqqNFIOlXsbnrFA130_head.
- NP1235327.RACNgG7f8CuCfRXR_S24tWRLdH_WjltqqNFIOlXsbnrFA130_assertion description "[Further studies, including reassessing family history in patients of primary CoQ10 deficiency for the possible occurrence of MSA, are now warranted to resolve the role of COQ2 variation in MSA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1235327.RACNgG7f8CuCfRXR_S24tWRLdH_WjltqqNFIOlXsbnrFA130_provenance.
- NP1235327.RACNgG7f8CuCfRXR_S24tWRLdH_WjltqqNFIOlXsbnrFA130_assertion evidence source_evidence_literature NP1235327.RACNgG7f8CuCfRXR_S24tWRLdH_WjltqqNFIOlXsbnrFA130_provenance.
- NP1235327.RACNgG7f8CuCfRXR_S24tWRLdH_WjltqqNFIOlXsbnrFA130_assertion SIO_000772 25373618 NP1235327.RACNgG7f8CuCfRXR_S24tWRLdH_WjltqqNFIOlXsbnrFA130_provenance.
- NP1235327.RACNgG7f8CuCfRXR_S24tWRLdH_WjltqqNFIOlXsbnrFA130_assertion wasDerivedFrom befree-2016 NP1235327.RACNgG7f8CuCfRXR_S24tWRLdH_WjltqqNFIOlXsbnrFA130_provenance.
- NP1235327.RACNgG7f8CuCfRXR_S24tWRLdH_WjltqqNFIOlXsbnrFA130_assertion wasGeneratedBy ECO_0000203 NP1235327.RACNgG7f8CuCfRXR_S24tWRLdH_WjltqqNFIOlXsbnrFA130_provenance.