Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP816061.RAFDMdwdkfT7rqZ_bZTjqfqQ-Q6IZsus7TNerT7048W7U130_assertion> ?p ?o ?g. }
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- NP816061.RAFDMdwdkfT7rqZ_bZTjqfqQ-Q6IZsus7TNerT7048W7U130_assertion type Assertion NP816061.RAFDMdwdkfT7rqZ_bZTjqfqQ-Q6IZsus7TNerT7048W7U130_head.
- NP816061.RAFDMdwdkfT7rqZ_bZTjqfqQ-Q6IZsus7TNerT7048W7U130_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." NP816061.RAFDMdwdkfT7rqZ_bZTjqfqQ-Q6IZsus7TNerT7048W7U130_provenance.
- NP816061.RAFDMdwdkfT7rqZ_bZTjqfqQ-Q6IZsus7TNerT7048W7U130_assertion evidence source_evidence_literature NP816061.RAFDMdwdkfT7rqZ_bZTjqfqQ-Q6IZsus7TNerT7048W7U130_provenance.
- NP816061.RAFDMdwdkfT7rqZ_bZTjqfqQ-Q6IZsus7TNerT7048W7U130_assertion SIO_000772 20516677 NP816061.RAFDMdwdkfT7rqZ_bZTjqfqQ-Q6IZsus7TNerT7048W7U130_provenance.
- NP816061.RAFDMdwdkfT7rqZ_bZTjqfqQ-Q6IZsus7TNerT7048W7U130_assertion wasDerivedFrom befree-2016 NP816061.RAFDMdwdkfT7rqZ_bZTjqfqQ-Q6IZsus7TNerT7048W7U130_provenance.
- NP816061.RAFDMdwdkfT7rqZ_bZTjqfqQ-Q6IZsus7TNerT7048W7U130_assertion wasGeneratedBy ECO_0000203 NP816061.RAFDMdwdkfT7rqZ_bZTjqfqQ-Q6IZsus7TNerT7048W7U130_provenance.