Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP418862.RA2jrcbv7g9daHd1E170MMq4jDswSbFzIXvKvKjG7oh7U130_assertion> ?p ?o ?g. }
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- NP418862.RA2jrcbv7g9daHd1E170MMq4jDswSbFzIXvKvKjG7oh7U130_assertion type Assertion NP418862.RA2jrcbv7g9daHd1E170MMq4jDswSbFzIXvKvKjG7oh7U130_head.
- NP418862.RA2jrcbv7g9daHd1E170MMq4jDswSbFzIXvKvKjG7oh7U130_assertion description "[Acquired somatic mutations in ATRX, an X-linked gene encoding a chromatin-associated protein, were recently identified in 4 patients with the rare subtype of myelodysplastic syndrome (MDS) associated with thalassemia (ATMDS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418862.RA2jrcbv7g9daHd1E170MMq4jDswSbFzIXvKvKjG7oh7U130_provenance.
- NP418862.RA2jrcbv7g9daHd1E170MMq4jDswSbFzIXvKvKjG7oh7U130_assertion evidence source_evidence_literature NP418862.RA2jrcbv7g9daHd1E170MMq4jDswSbFzIXvKvKjG7oh7U130_provenance.
- NP418862.RA2jrcbv7g9daHd1E170MMq4jDswSbFzIXvKvKjG7oh7U130_assertion SIO_000772 14592816 NP418862.RA2jrcbv7g9daHd1E170MMq4jDswSbFzIXvKvKjG7oh7U130_provenance.
- NP418862.RA2jrcbv7g9daHd1E170MMq4jDswSbFzIXvKvKjG7oh7U130_assertion wasDerivedFrom befree-2016 NP418862.RA2jrcbv7g9daHd1E170MMq4jDswSbFzIXvKvKjG7oh7U130_provenance.
- NP418862.RA2jrcbv7g9daHd1E170MMq4jDswSbFzIXvKvKjG7oh7U130_assertion wasGeneratedBy ECO_0000203 NP418862.RA2jrcbv7g9daHd1E170MMq4jDswSbFzIXvKvKjG7oh7U130_provenance.