Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP247900.RA9OKZ5i5iyCefwugGebjM8_Jft5oTaHRo8jye9Xre2Zc130_assertion> ?p ?o ?g. }
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- NP247900.RA9OKZ5i5iyCefwugGebjM8_Jft5oTaHRo8jye9Xre2Zc130_assertion type Assertion NP247900.RA9OKZ5i5iyCefwugGebjM8_Jft5oTaHRo8jye9Xre2Zc130_head.
- NP247900.RA9OKZ5i5iyCefwugGebjM8_Jft5oTaHRo8jye9Xre2Zc130_assertion description "[Megaloblastic anaemia 1 (MGA1, OMIM 261100) is a rare, autosomal recessive disorder characterized by juvenile megaloblastic anaemia, as well as neurological symptoms that may be the only manifestations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP247900.RA9OKZ5i5iyCefwugGebjM8_Jft5oTaHRo8jye9Xre2Zc130_provenance.
- NP247900.RA9OKZ5i5iyCefwugGebjM8_Jft5oTaHRo8jye9Xre2Zc130_assertion evidence source_evidence_literature NP247900.RA9OKZ5i5iyCefwugGebjM8_Jft5oTaHRo8jye9Xre2Zc130_provenance.
- NP247900.RA9OKZ5i5iyCefwugGebjM8_Jft5oTaHRo8jye9Xre2Zc130_assertion SIO_000772 10080186 NP247900.RA9OKZ5i5iyCefwugGebjM8_Jft5oTaHRo8jye9Xre2Zc130_provenance.
- NP247900.RA9OKZ5i5iyCefwugGebjM8_Jft5oTaHRo8jye9Xre2Zc130_assertion wasDerivedFrom befree-2016 NP247900.RA9OKZ5i5iyCefwugGebjM8_Jft5oTaHRo8jye9Xre2Zc130_provenance.
- NP247900.RA9OKZ5i5iyCefwugGebjM8_Jft5oTaHRo8jye9Xre2Zc130_assertion wasGeneratedBy ECO_0000203 NP247900.RA9OKZ5i5iyCefwugGebjM8_Jft5oTaHRo8jye9Xre2Zc130_provenance.