Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP697293.RAXjWo1ZrFgTHXaJ0KixBMyKDAj668VdNqu2eIILx-cUA130_assertion> ?p ?o ?g. }
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- NP697293.RAXjWo1ZrFgTHXaJ0KixBMyKDAj668VdNqu2eIILx-cUA130_assertion type Assertion NP697293.RAXjWo1ZrFgTHXaJ0KixBMyKDAj668VdNqu2eIILx-cUA130_head.
- NP697293.RAXjWo1ZrFgTHXaJ0KixBMyKDAj668VdNqu2eIILx-cUA130_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." NP697293.RAXjWo1ZrFgTHXaJ0KixBMyKDAj668VdNqu2eIILx-cUA130_provenance.
- NP697293.RAXjWo1ZrFgTHXaJ0KixBMyKDAj668VdNqu2eIILx-cUA130_assertion evidence source_evidence_literature NP697293.RAXjWo1ZrFgTHXaJ0KixBMyKDAj668VdNqu2eIILx-cUA130_provenance.
- NP697293.RAXjWo1ZrFgTHXaJ0KixBMyKDAj668VdNqu2eIILx-cUA130_assertion SIO_000772 18266205 NP697293.RAXjWo1ZrFgTHXaJ0KixBMyKDAj668VdNqu2eIILx-cUA130_provenance.
- NP697293.RAXjWo1ZrFgTHXaJ0KixBMyKDAj668VdNqu2eIILx-cUA130_assertion wasDerivedFrom befree-20150227 NP697293.RAXjWo1ZrFgTHXaJ0KixBMyKDAj668VdNqu2eIILx-cUA130_provenance.
- NP697293.RAXjWo1ZrFgTHXaJ0KixBMyKDAj668VdNqu2eIILx-cUA130_assertion wasGeneratedBy ECO_0000203 NP697293.RAXjWo1ZrFgTHXaJ0KixBMyKDAj668VdNqu2eIILx-cUA130_provenance.