Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP883648.RA5y0R9qjnbHysHTREyQLRYeBwcsKLacAqg6NKl153l8Q130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP883648.RA5y0R9qjnbHysHTREyQLRYeBwcsKLacAqg6NKl153l8Q130_assertion type Assertion NP883648.RA5y0R9qjnbHysHTREyQLRYeBwcsKLacAqg6NKl153l8Q130_head.
- NP883648.RA5y0R9qjnbHysHTREyQLRYeBwcsKLacAqg6NKl153l8Q130_assertion description "[The frequencies of the host genetic factors in the whole group were 0.52 for blood group O, 0.13 for hemoglobin S, 0.16 for the G6PD A-deficient variant and 0.24 for alpha+-thalassemia (-alpha(3.7) deletion).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP883648.RA5y0R9qjnbHysHTREyQLRYeBwcsKLacAqg6NKl153l8Q130_provenance.
- NP883648.RA5y0R9qjnbHysHTREyQLRYeBwcsKLacAqg6NKl153l8Q130_assertion evidence source_evidence_literature NP883648.RA5y0R9qjnbHysHTREyQLRYeBwcsKLacAqg6NKl153l8Q130_provenance.
- NP883648.RA5y0R9qjnbHysHTREyQLRYeBwcsKLacAqg6NKl153l8Q130_assertion SIO_000772 16859949 NP883648.RA5y0R9qjnbHysHTREyQLRYeBwcsKLacAqg6NKl153l8Q130_provenance.
- NP883648.RA5y0R9qjnbHysHTREyQLRYeBwcsKLacAqg6NKl153l8Q130_assertion wasDerivedFrom befree-20140225 NP883648.RA5y0R9qjnbHysHTREyQLRYeBwcsKLacAqg6NKl153l8Q130_provenance.
- NP883648.RA5y0R9qjnbHysHTREyQLRYeBwcsKLacAqg6NKl153l8Q130_assertion wasGeneratedBy ECO_0000203 NP883648.RA5y0R9qjnbHysHTREyQLRYeBwcsKLacAqg6NKl153l8Q130_provenance.