Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP373465.RAlMg9jCNhIR5iTnKunicNdr7WgiJoS0rflmLZHwXeUns130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP373465.RAlMg9jCNhIR5iTnKunicNdr7WgiJoS0rflmLZHwXeUns130_assertion type Assertion NP373465.RAlMg9jCNhIR5iTnKunicNdr7WgiJoS0rflmLZHwXeUns130_head.
- NP373465.RAlMg9jCNhIR5iTnKunicNdr7WgiJoS0rflmLZHwXeUns130_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." NP373465.RAlMg9jCNhIR5iTnKunicNdr7WgiJoS0rflmLZHwXeUns130_provenance.
- NP373465.RAlMg9jCNhIR5iTnKunicNdr7WgiJoS0rflmLZHwXeUns130_assertion evidence source_evidence_literature NP373465.RAlMg9jCNhIR5iTnKunicNdr7WgiJoS0rflmLZHwXeUns130_provenance.
- NP373465.RAlMg9jCNhIR5iTnKunicNdr7WgiJoS0rflmLZHwXeUns130_assertion SIO_000772 10080186 NP373465.RAlMg9jCNhIR5iTnKunicNdr7WgiJoS0rflmLZHwXeUns130_provenance.
- NP373465.RAlMg9jCNhIR5iTnKunicNdr7WgiJoS0rflmLZHwXeUns130_assertion wasDerivedFrom befree-20140225 NP373465.RAlMg9jCNhIR5iTnKunicNdr7WgiJoS0rflmLZHwXeUns130_provenance.
- NP373465.RAlMg9jCNhIR5iTnKunicNdr7WgiJoS0rflmLZHwXeUns130_assertion wasGeneratedBy ECO_0000203 NP373465.RAlMg9jCNhIR5iTnKunicNdr7WgiJoS0rflmLZHwXeUns130_provenance.