Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP924037.RAVmyX7g8ym4CSBxB9ImdYz9xydaUoYVd9pLBuaoDfoXo130_assertion> ?p ?o ?g. }
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- NP924037.RAVmyX7g8ym4CSBxB9ImdYz9xydaUoYVd9pLBuaoDfoXo130_assertion type Assertion NP924037.RAVmyX7g8ym4CSBxB9ImdYz9xydaUoYVd9pLBuaoDfoXo130_head.
- NP924037.RAVmyX7g8ym4CSBxB9ImdYz9xydaUoYVd9pLBuaoDfoXo130_assertion description "[In Finland MES is effectively screened and relatively frequent with a birth prevalence of 1:9,000 and a disease gene frequency of 0.01 (ref.4) which is of the same order of magnitude as that of the most common recessive diseases belonging to the 'Finnish disease heritage', that is genetic disorders enriched or only encountered in Finland.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP924037.RAVmyX7g8ym4CSBxB9ImdYz9xydaUoYVd9pLBuaoDfoXo130_provenance.
- NP924037.RAVmyX7g8ym4CSBxB9ImdYz9xydaUoYVd9pLBuaoDfoXo130_assertion evidence source_evidence_literature NP924037.RAVmyX7g8ym4CSBxB9ImdYz9xydaUoYVd9pLBuaoDfoXo130_provenance.
- NP924037.RAVmyX7g8ym4CSBxB9ImdYz9xydaUoYVd9pLBuaoDfoXo130_assertion SIO_000772 7550354 NP924037.RAVmyX7g8ym4CSBxB9ImdYz9xydaUoYVd9pLBuaoDfoXo130_provenance.
- NP924037.RAVmyX7g8ym4CSBxB9ImdYz9xydaUoYVd9pLBuaoDfoXo130_assertion wasDerivedFrom befree-20140225 NP924037.RAVmyX7g8ym4CSBxB9ImdYz9xydaUoYVd9pLBuaoDfoXo130_provenance.
- NP924037.RAVmyX7g8ym4CSBxB9ImdYz9xydaUoYVd9pLBuaoDfoXo130_assertion wasGeneratedBy ECO_0000203 NP924037.RAVmyX7g8ym4CSBxB9ImdYz9xydaUoYVd9pLBuaoDfoXo130_provenance.