Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP636450.RABg9D7aPtOnBY9Gaqm4EAITFpUJHJtB_drKKZkNfai2U130_assertion> ?p ?o ?g. }
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- NP636450.RABg9D7aPtOnBY9Gaqm4EAITFpUJHJtB_drKKZkNfai2U130_assertion type Assertion NP636450.RABg9D7aPtOnBY9Gaqm4EAITFpUJHJtB_drKKZkNfai2U130_head.
- NP636450.RABg9D7aPtOnBY9Gaqm4EAITFpUJHJtB_drKKZkNfai2U130_assertion wasGeneratedBy ECO_0000203 NP636450.RABg9D7aPtOnBY9Gaqm4EAITFpUJHJtB_drKKZkNfai2U130_provenance.
- NP636450.RABg9D7aPtOnBY9Gaqm4EAITFpUJHJtB_drKKZkNfai2U130_assertion wasDerivedFrom befree-20150227 NP636450.RABg9D7aPtOnBY9Gaqm4EAITFpUJHJtB_drKKZkNfai2U130_provenance.
- NP636450.RABg9D7aPtOnBY9Gaqm4EAITFpUJHJtB_drKKZkNfai2U130_assertion SIO_000772 21877956 NP636450.RABg9D7aPtOnBY9Gaqm4EAITFpUJHJtB_drKKZkNfai2U130_provenance.
- NP636450.RABg9D7aPtOnBY9Gaqm4EAITFpUJHJtB_drKKZkNfai2U130_assertion evidence source_evidence_literature NP636450.RABg9D7aPtOnBY9Gaqm4EAITFpUJHJtB_drKKZkNfai2U130_provenance.
- NP636450.RABg9D7aPtOnBY9Gaqm4EAITFpUJHJtB_drKKZkNfai2U130_assertion description "[The rare g allele for L162V was found in 15% of patients free of any sign of lipodystrophy and 8% with at least one sign of lipodystrophy (p=0.04) and the rare t allele for H449H was found in 14% of patients free of any sign of lipodystrophy and 23% of patients with at least one sign of lipodystrophy (p=0.05).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP636450.RABg9D7aPtOnBY9Gaqm4EAITFpUJHJtB_drKKZkNfai2U130_provenance.