Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP443829.RA8sLEkwQumfVWQ3-1Uz1vusU56aSHjZAgeobqqB0bxc0130_assertion> ?p ?o ?g. }
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- NP443829.RA8sLEkwQumfVWQ3-1Uz1vusU56aSHjZAgeobqqB0bxc0130_assertion type Assertion NP443829.RA8sLEkwQumfVWQ3-1Uz1vusU56aSHjZAgeobqqB0bxc0130_head.
- NP443829.RA8sLEkwQumfVWQ3-1Uz1vusU56aSHjZAgeobqqB0bxc0130_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." NP443829.RA8sLEkwQumfVWQ3-1Uz1vusU56aSHjZAgeobqqB0bxc0130_provenance.
- NP443829.RA8sLEkwQumfVWQ3-1Uz1vusU56aSHjZAgeobqqB0bxc0130_assertion evidence source_evidence_literature NP443829.RA8sLEkwQumfVWQ3-1Uz1vusU56aSHjZAgeobqqB0bxc0130_provenance.
- NP443829.RA8sLEkwQumfVWQ3-1Uz1vusU56aSHjZAgeobqqB0bxc0130_assertion SIO_000772 20691621 NP443829.RA8sLEkwQumfVWQ3-1Uz1vusU56aSHjZAgeobqqB0bxc0130_provenance.
- NP443829.RA8sLEkwQumfVWQ3-1Uz1vusU56aSHjZAgeobqqB0bxc0130_assertion wasDerivedFrom befree-20150227 NP443829.RA8sLEkwQumfVWQ3-1Uz1vusU56aSHjZAgeobqqB0bxc0130_provenance.
- NP443829.RA8sLEkwQumfVWQ3-1Uz1vusU56aSHjZAgeobqqB0bxc0130_assertion wasGeneratedBy ECO_0000203 NP443829.RA8sLEkwQumfVWQ3-1Uz1vusU56aSHjZAgeobqqB0bxc0130_provenance.