Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP424419.RAAPj39GXOImH8xvHbk2LYKj3B-tvoCIVC7_wTSFvjat0130_assertion> ?p ?o ?g. }
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- NP424419.RAAPj39GXOImH8xvHbk2LYKj3B-tvoCIVC7_wTSFvjat0130_assertion type Assertion NP424419.RAAPj39GXOImH8xvHbk2LYKj3B-tvoCIVC7_wTSFvjat0130_head.
- NP424419.RAAPj39GXOImH8xvHbk2LYKj3B-tvoCIVC7_wTSFvjat0130_assertion description "[These results indicate a significant modification of the phenotype of FH with defective LDLR allele by EPHX2-287Arg variation in our studied kindred.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP424419.RAAPj39GXOImH8xvHbk2LYKj3B-tvoCIVC7_wTSFvjat0130_provenance.
- NP424419.RAAPj39GXOImH8xvHbk2LYKj3B-tvoCIVC7_wTSFvjat0130_assertion evidence source_evidence_literature NP424419.RAAPj39GXOImH8xvHbk2LYKj3B-tvoCIVC7_wTSFvjat0130_provenance.
- NP424419.RAAPj39GXOImH8xvHbk2LYKj3B-tvoCIVC7_wTSFvjat0130_assertion SIO_000772 14673705 NP424419.RAAPj39GXOImH8xvHbk2LYKj3B-tvoCIVC7_wTSFvjat0130_provenance.
- NP424419.RAAPj39GXOImH8xvHbk2LYKj3B-tvoCIVC7_wTSFvjat0130_assertion wasDerivedFrom befree-2016 NP424419.RAAPj39GXOImH8xvHbk2LYKj3B-tvoCIVC7_wTSFvjat0130_provenance.
- NP424419.RAAPj39GXOImH8xvHbk2LYKj3B-tvoCIVC7_wTSFvjat0130_assertion wasGeneratedBy ECO_0000203 NP424419.RAAPj39GXOImH8xvHbk2LYKj3B-tvoCIVC7_wTSFvjat0130_provenance.