Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP442206.RAPodYSmVhymh0DUjjjCdCUXpWIFSpzEmylToxtSV3vhQ130_assertion> ?p ?o ?g. }
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- NP442206.RAPodYSmVhymh0DUjjjCdCUXpWIFSpzEmylToxtSV3vhQ130_assertion type Assertion NP442206.RAPodYSmVhymh0DUjjjCdCUXpWIFSpzEmylToxtSV3vhQ130_head.
- NP442206.RAPodYSmVhymh0DUjjjCdCUXpWIFSpzEmylToxtSV3vhQ130_assertion description "[A comparison of several statistical methods and measures (gene frequency, haplotype frequency, and linkage disequilibrium estimation) using the Centre d'Etude du Polymorphisme Humain data will be provided using KIR haplotypes that have been determined by segregation analysis, noting the strengths and weaknesses of the methods when only the presence/absence data is considered.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP442206.RAPodYSmVhymh0DUjjjCdCUXpWIFSpzEmylToxtSV3vhQ130_provenance.
- NP442206.RAPodYSmVhymh0DUjjjCdCUXpWIFSpzEmylToxtSV3vhQ130_assertion evidence source_evidence_literature NP442206.RAPodYSmVhymh0DUjjjCdCUXpWIFSpzEmylToxtSV3vhQ130_provenance.
- NP442206.RAPodYSmVhymh0DUjjjCdCUXpWIFSpzEmylToxtSV3vhQ130_assertion SIO_000772 18797862 NP442206.RAPodYSmVhymh0DUjjjCdCUXpWIFSpzEmylToxtSV3vhQ130_provenance.
- NP442206.RAPodYSmVhymh0DUjjjCdCUXpWIFSpzEmylToxtSV3vhQ130_assertion wasDerivedFrom befree-20140225 NP442206.RAPodYSmVhymh0DUjjjCdCUXpWIFSpzEmylToxtSV3vhQ130_provenance.
- NP442206.RAPodYSmVhymh0DUjjjCdCUXpWIFSpzEmylToxtSV3vhQ130_assertion wasGeneratedBy ECO_0000203 NP442206.RAPodYSmVhymh0DUjjjCdCUXpWIFSpzEmylToxtSV3vhQ130_provenance.