Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP665718.RAuh_6bZUb0nGFxHC9W6Dw5U_93TpJwC-Oka2zWpb020U130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP665718.RAuh_6bZUb0nGFxHC9W6Dw5U_93TpJwC-Oka2zWpb020U130_assertion type Assertion NP665718.RAuh_6bZUb0nGFxHC9W6Dw5U_93TpJwC-Oka2zWpb020U130_head.
- NP665718.RAuh_6bZUb0nGFxHC9W6Dw5U_93TpJwC-Oka2zWpb020U130_assertion description "[Of these 12 patients, three had homozygous G701D/G701D and heterozygous Hb E; one compound heterozygous SAO/G701D and heterozygous alpha(+)-thalassemia; and one compound heterozygous G701D/A858D and heterozygous Hb E. Of 6 patients without SLC4A1 mutation, two each carried heterozygous or homozygous Hb E and one of the latter also had Hb H disease (--(SEA)/-alpha(4.2)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP665718.RAuh_6bZUb0nGFxHC9W6Dw5U_93TpJwC-Oka2zWpb020U130_provenance.
- NP665718.RAuh_6bZUb0nGFxHC9W6Dw5U_93TpJwC-Oka2zWpb020U130_assertion evidence source_evidence_literature NP665718.RAuh_6bZUb0nGFxHC9W6Dw5U_93TpJwC-Oka2zWpb020U130_provenance.
- NP665718.RAuh_6bZUb0nGFxHC9W6Dw5U_93TpJwC-Oka2zWpb020U130_assertion SIO_000772 18266205 NP665718.RAuh_6bZUb0nGFxHC9W6Dw5U_93TpJwC-Oka2zWpb020U130_provenance.
- NP665718.RAuh_6bZUb0nGFxHC9W6Dw5U_93TpJwC-Oka2zWpb020U130_assertion wasDerivedFrom befree-20140225 NP665718.RAuh_6bZUb0nGFxHC9W6Dw5U_93TpJwC-Oka2zWpb020U130_provenance.
- NP665718.RAuh_6bZUb0nGFxHC9W6Dw5U_93TpJwC-Oka2zWpb020U130_assertion wasGeneratedBy ECO_0000203 NP665718.RAuh_6bZUb0nGFxHC9W6Dw5U_93TpJwC-Oka2zWpb020U130_provenance.