Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP643395.RAk01BFYQv1caYqoQ2ysjgxENfo7c5rcdyOGEi1sEqXmM130_assertion> ?p ?o ?g. }
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- NP643395.RAk01BFYQv1caYqoQ2ysjgxENfo7c5rcdyOGEi1sEqXmM130_assertion type Assertion NP643395.RAk01BFYQv1caYqoQ2ysjgxENfo7c5rcdyOGEi1sEqXmM130_head.
- NP643395.RAk01BFYQv1caYqoQ2ysjgxENfo7c5rcdyOGEi1sEqXmM130_assertion description "[Although a rare disorder, the frequency of FXI deficiency is high in certain populations, notably persons of Ashkenazi descent and the Basque population of Southern France.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP643395.RAk01BFYQv1caYqoQ2ysjgxENfo7c5rcdyOGEi1sEqXmM130_provenance.
- NP643395.RAk01BFYQv1caYqoQ2ysjgxENfo7c5rcdyOGEi1sEqXmM130_assertion evidence source_evidence_literature NP643395.RAk01BFYQv1caYqoQ2ysjgxENfo7c5rcdyOGEi1sEqXmM130_provenance.
- NP643395.RAk01BFYQv1caYqoQ2ysjgxENfo7c5rcdyOGEi1sEqXmM130_assertion SIO_000772 14872426 NP643395.RAk01BFYQv1caYqoQ2ysjgxENfo7c5rcdyOGEi1sEqXmM130_provenance.
- NP643395.RAk01BFYQv1caYqoQ2ysjgxENfo7c5rcdyOGEi1sEqXmM130_assertion wasDerivedFrom befree-20140225 NP643395.RAk01BFYQv1caYqoQ2ysjgxENfo7c5rcdyOGEi1sEqXmM130_provenance.
- NP643395.RAk01BFYQv1caYqoQ2ysjgxENfo7c5rcdyOGEi1sEqXmM130_assertion wasGeneratedBy ECO_0000203 NP643395.RAk01BFYQv1caYqoQ2ysjgxENfo7c5rcdyOGEi1sEqXmM130_provenance.