Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP88363.RABohPkUilFjqIhdLH7gVidx9IVLVSvt6e8SUW7HmCHro130_assertion> ?p ?o ?g. }
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- NP88363.RABohPkUilFjqIhdLH7gVidx9IVLVSvt6e8SUW7HmCHro130_assertion type Assertion NP88363.RABohPkUilFjqIhdLH7gVidx9IVLVSvt6e8SUW7HmCHro130_head.
- NP88363.RABohPkUilFjqIhdLH7gVidx9IVLVSvt6e8SUW7HmCHro130_assertion description "[The only POR missense polymorphism found in atypical 21OHD patients was A503V.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP88363.RABohPkUilFjqIhdLH7gVidx9IVLVSvt6e8SUW7HmCHro130_provenance.
- NP88363.RABohPkUilFjqIhdLH7gVidx9IVLVSvt6e8SUW7HmCHro130_assertion evidence source_evidence_literature NP88363.RABohPkUilFjqIhdLH7gVidx9IVLVSvt6e8SUW7HmCHro130_provenance.
- NP88363.RABohPkUilFjqIhdLH7gVidx9IVLVSvt6e8SUW7HmCHro130_assertion SIO_000772 18397975 NP88363.RABohPkUilFjqIhdLH7gVidx9IVLVSvt6e8SUW7HmCHro130_provenance.
- NP88363.RABohPkUilFjqIhdLH7gVidx9IVLVSvt6e8SUW7HmCHro130_assertion wasDerivedFrom gad-20150221 NP88363.RABohPkUilFjqIhdLH7gVidx9IVLVSvt6e8SUW7HmCHro130_provenance.
- NP88363.RABohPkUilFjqIhdLH7gVidx9IVLVSvt6e8SUW7HmCHro130_assertion wasGeneratedBy ECO_0000203 NP88363.RABohPkUilFjqIhdLH7gVidx9IVLVSvt6e8SUW7HmCHro130_provenance.