Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP247899.RAJa6OsXJYYRX7hqzM8zr0Nu0E2P7wkneqIgjcywqUwa0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP247899.RAJa6OsXJYYRX7hqzM8zr0Nu0E2P7wkneqIgjcywqUwa0130_assertion type Assertion NP247899.RAJa6OsXJYYRX7hqzM8zr0Nu0E2P7wkneqIgjcywqUwa0130_head.
- NP247899.RAJa6OsXJYYRX7hqzM8zr0Nu0E2P7wkneqIgjcywqUwa0130_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." NP247899.RAJa6OsXJYYRX7hqzM8zr0Nu0E2P7wkneqIgjcywqUwa0130_provenance.
- NP247899.RAJa6OsXJYYRX7hqzM8zr0Nu0E2P7wkneqIgjcywqUwa0130_assertion evidence source_evidence_literature NP247899.RAJa6OsXJYYRX7hqzM8zr0Nu0E2P7wkneqIgjcywqUwa0130_provenance.
- NP247899.RAJa6OsXJYYRX7hqzM8zr0Nu0E2P7wkneqIgjcywqUwa0130_assertion SIO_000772 10080186 NP247899.RAJa6OsXJYYRX7hqzM8zr0Nu0E2P7wkneqIgjcywqUwa0130_provenance.
- NP247899.RAJa6OsXJYYRX7hqzM8zr0Nu0E2P7wkneqIgjcywqUwa0130_assertion wasDerivedFrom befree-2016 NP247899.RAJa6OsXJYYRX7hqzM8zr0Nu0E2P7wkneqIgjcywqUwa0130_provenance.
- NP247899.RAJa6OsXJYYRX7hqzM8zr0Nu0E2P7wkneqIgjcywqUwa0130_assertion wasGeneratedBy ECO_0000203 NP247899.RAJa6OsXJYYRX7hqzM8zr0Nu0E2P7wkneqIgjcywqUwa0130_provenance.