Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP247900.RA9OKZ5i5iyCefwugGebjM8_Jft5oTaHRo8jye9Xre2Zc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP247900.RA9OKZ5i5iyCefwugGebjM8_Jft5oTaHRo8jye9Xre2Zc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP247900.RA9OKZ5i5iyCefwugGebjM8_Jft5oTaHRo8jye9Xre2Zc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP247900.RA9OKZ5i5iyCefwugGebjM8_Jft5oTaHRo8jye9Xre2Zc130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP247900.RA9OKZ5i5iyCefwugGebjM8_Jft5oTaHRo8jye9Xre2Zc130_provenance.