Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP687749.RAhqOgn9moGTnaZeE8F8wk81rdWYMf_ycOGIQCXy8RoTU130_assertion> ?p ?o ?g. }
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- NP687749.RAhqOgn9moGTnaZeE8F8wk81rdWYMf_ycOGIQCXy8RoTU130_assertion type Assertion NP687749.RAhqOgn9moGTnaZeE8F8wk81rdWYMf_ycOGIQCXy8RoTU130_head.
- NP687749.RAhqOgn9moGTnaZeE8F8wk81rdWYMf_ycOGIQCXy8RoTU130_assertion wasGeneratedBy ECO_0000203 NP687749.RAhqOgn9moGTnaZeE8F8wk81rdWYMf_ycOGIQCXy8RoTU130_provenance.
- NP687749.RAhqOgn9moGTnaZeE8F8wk81rdWYMf_ycOGIQCXy8RoTU130_assertion wasDerivedFrom befree-20140225 NP687749.RAhqOgn9moGTnaZeE8F8wk81rdWYMf_ycOGIQCXy8RoTU130_provenance.
- NP687749.RAhqOgn9moGTnaZeE8F8wk81rdWYMf_ycOGIQCXy8RoTU130_assertion SIO_000772 20516677 NP687749.RAhqOgn9moGTnaZeE8F8wk81rdWYMf_ycOGIQCXy8RoTU130_provenance.
- NP687749.RAhqOgn9moGTnaZeE8F8wk81rdWYMf_ycOGIQCXy8RoTU130_assertion evidence source_evidence_literature NP687749.RAhqOgn9moGTnaZeE8F8wk81rdWYMf_ycOGIQCXy8RoTU130_provenance.
- NP687749.RAhqOgn9moGTnaZeE8F8wk81rdWYMf_ycOGIQCXy8RoTU130_assertion description "[Nondeletional hemoglobin (Hb) H disease is caused by a deletion of both alpha-globin genes on one chromosome 16 and of an alpha(+)-thalassemia point mutation on the other chromosome 16.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP687749.RAhqOgn9moGTnaZeE8F8wk81rdWYMf_ycOGIQCXy8RoTU130_provenance.