Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP831346.RArVeUafs0EkPwU3M8GzS2iVZhn1AM0AOx6fmhDbkiubM130_assertion> ?p ?o ?g. }
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- NP831346.RArVeUafs0EkPwU3M8GzS2iVZhn1AM0AOx6fmhDbkiubM130_assertion type Assertion NP831346.RArVeUafs0EkPwU3M8GzS2iVZhn1AM0AOx6fmhDbkiubM130_head.
- NP831346.RArVeUafs0EkPwU3M8GzS2iVZhn1AM0AOx6fmhDbkiubM130_assertion description "[Hemoglobin H disease due to a de novo mutation at the ?2-globin gene and an inherited common ?-thalassemia deletion found in a Chinese boy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP831346.RArVeUafs0EkPwU3M8GzS2iVZhn1AM0AOx6fmhDbkiubM130_provenance.
- NP831346.RArVeUafs0EkPwU3M8GzS2iVZhn1AM0AOx6fmhDbkiubM130_assertion evidence source_evidence_literature NP831346.RArVeUafs0EkPwU3M8GzS2iVZhn1AM0AOx6fmhDbkiubM130_provenance.
- NP831346.RArVeUafs0EkPwU3M8GzS2iVZhn1AM0AOx6fmhDbkiubM130_assertion SIO_000772 20691621 NP831346.RArVeUafs0EkPwU3M8GzS2iVZhn1AM0AOx6fmhDbkiubM130_provenance.
- NP831346.RArVeUafs0EkPwU3M8GzS2iVZhn1AM0AOx6fmhDbkiubM130_assertion wasDerivedFrom befree-2016 NP831346.RArVeUafs0EkPwU3M8GzS2iVZhn1AM0AOx6fmhDbkiubM130_provenance.
- NP831346.RArVeUafs0EkPwU3M8GzS2iVZhn1AM0AOx6fmhDbkiubM130_assertion wasGeneratedBy ECO_0000203 NP831346.RArVeUafs0EkPwU3M8GzS2iVZhn1AM0AOx6fmhDbkiubM130_provenance.