Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP786781.RAVgq9M9WGclG3pG4EaogDpUtXQIi6zj18fYBBwol-gMc130_assertion> ?p ?o ?g. }
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- NP786781.RAVgq9M9WGclG3pG4EaogDpUtXQIi6zj18fYBBwol-gMc130_assertion type Assertion NP786781.RAVgq9M9WGclG3pG4EaogDpUtXQIi6zj18fYBBwol-gMc130_head.
- NP786781.RAVgq9M9WGclG3pG4EaogDpUtXQIi6zj18fYBBwol-gMc130_assertion description "[Thiamine-responsive megaloblastic anemia (TRMA, also known as Rogers syndrome, OMIM 249270) is a rare autosomal recessive disorder characterized by a triad of megaloblastic anemia, diabetes mellitus, and sensorineural deafness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP786781.RAVgq9M9WGclG3pG4EaogDpUtXQIi6zj18fYBBwol-gMc130_provenance.
- NP786781.RAVgq9M9WGclG3pG4EaogDpUtXQIi6zj18fYBBwol-gMc130_assertion evidence source_evidence_literature NP786781.RAVgq9M9WGclG3pG4EaogDpUtXQIi6zj18fYBBwol-gMc130_provenance.
- NP786781.RAVgq9M9WGclG3pG4EaogDpUtXQIi6zj18fYBBwol-gMc130_assertion SIO_000772 9856490 NP786781.RAVgq9M9WGclG3pG4EaogDpUtXQIi6zj18fYBBwol-gMc130_provenance.
- NP786781.RAVgq9M9WGclG3pG4EaogDpUtXQIi6zj18fYBBwol-gMc130_assertion wasDerivedFrom befree-20140225 NP786781.RAVgq9M9WGclG3pG4EaogDpUtXQIi6zj18fYBBwol-gMc130_provenance.
- NP786781.RAVgq9M9WGclG3pG4EaogDpUtXQIi6zj18fYBBwol-gMc130_assertion wasGeneratedBy ECO_0000203 NP786781.RAVgq9M9WGclG3pG4EaogDpUtXQIi6zj18fYBBwol-gMc130_provenance.