Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP59229.RAEDIfriEZ78T78raoKUQOezhWYMeYd8rPhNf26U2OKR4130_assertion> ?p ?o ?g. }
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- NP59229.RAEDIfriEZ78T78raoKUQOezhWYMeYd8rPhNf26U2OKR4130_assertion type Assertion NP59229.RAEDIfriEZ78T78raoKUQOezhWYMeYd8rPhNf26U2OKR4130_head.
- NP59229.RAEDIfriEZ78T78raoKUQOezhWYMeYd8rPhNf26U2OKR4130_assertion wasGeneratedBy ECO_0000203 NP59229.RAEDIfriEZ78T78raoKUQOezhWYMeYd8rPhNf26U2OKR4130_provenance.
- NP59229.RAEDIfriEZ78T78raoKUQOezhWYMeYd8rPhNf26U2OKR4130_assertion wasDerivedFrom gad-20130706 NP59229.RAEDIfriEZ78T78raoKUQOezhWYMeYd8rPhNf26U2OKR4130_provenance.
- NP59229.RAEDIfriEZ78T78raoKUQOezhWYMeYd8rPhNf26U2OKR4130_assertion SIO_000772 14604959 NP59229.RAEDIfriEZ78T78raoKUQOezhWYMeYd8rPhNf26U2OKR4130_provenance.
- NP59229.RAEDIfriEZ78T78raoKUQOezhWYMeYd8rPhNf26U2OKR4130_assertion evidence source_evidence_literature NP59229.RAEDIfriEZ78T78raoKUQOezhWYMeYd8rPhNf26U2OKR4130_provenance.
- NP59229.RAEDIfriEZ78T78raoKUQOezhWYMeYd8rPhNf26U2OKR4130_assertion description "[We conclude that the VHL 598C>T mutation, the most common defect of congenital polycythemia yet found, was spread from a single founder 1,000 to 62,000 years ago.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59229.RAEDIfriEZ78T78raoKUQOezhWYMeYd8rPhNf26U2OKR4130_provenance.