Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1347030.RAFpGPOdWmPRPRjfi1mYc7LPLc0hb2XIr419Bl9lJvWvk130_assertion> ?p ?o ?g. }
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- NP1347030.RAFpGPOdWmPRPRjfi1mYc7LPLc0hb2XIr419Bl9lJvWvk130_assertion type Assertion NP1347030.RAFpGPOdWmPRPRjfi1mYc7LPLc0hb2XIr419Bl9lJvWvk130_head.
- NP1347030.RAFpGPOdWmPRPRjfi1mYc7LPLc0hb2XIr419Bl9lJvWvk130_assertion description "[More recently, FBN1 has also been shown to harbor mutations related to a spectrum of conditions phenotypically related to MFS and many mutations will have to be accumulated before genotype/phenotype relationships emerge.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1347030.RAFpGPOdWmPRPRjfi1mYc7LPLc0hb2XIr419Bl9lJvWvk130_provenance.
- NP1347030.RAFpGPOdWmPRPRjfi1mYc7LPLc0hb2XIr419Bl9lJvWvk130_assertion evidence source_evidence_literature NP1347030.RAFpGPOdWmPRPRjfi1mYc7LPLc0hb2XIr419Bl9lJvWvk130_provenance.
- NP1347030.RAFpGPOdWmPRPRjfi1mYc7LPLc0hb2XIr419Bl9lJvWvk130_assertion SIO_000772 8594563 NP1347030.RAFpGPOdWmPRPRjfi1mYc7LPLc0hb2XIr419Bl9lJvWvk130_provenance.
- NP1347030.RAFpGPOdWmPRPRjfi1mYc7LPLc0hb2XIr419Bl9lJvWvk130_assertion wasDerivedFrom befree-2016 NP1347030.RAFpGPOdWmPRPRjfi1mYc7LPLc0hb2XIr419Bl9lJvWvk130_provenance.
- NP1347030.RAFpGPOdWmPRPRjfi1mYc7LPLc0hb2XIr419Bl9lJvWvk130_assertion wasGeneratedBy ECO_0000203 NP1347030.RAFpGPOdWmPRPRjfi1mYc7LPLc0hb2XIr419Bl9lJvWvk130_provenance.