Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP618352.RAXHZmqV7eBEgPklTl14-ixuRYt-h-Tw1_kPhT5K5fQWI130_assertion> ?p ?o ?g. }
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- NP618352.RAXHZmqV7eBEgPklTl14-ixuRYt-h-Tw1_kPhT5K5fQWI130_assertion type Assertion NP618352.RAXHZmqV7eBEgPklTl14-ixuRYt-h-Tw1_kPhT5K5fQWI130_head.
- NP618352.RAXHZmqV7eBEgPklTl14-ixuRYt-h-Tw1_kPhT5K5fQWI130_assertion description "[The chromatin-associated protein ATRX was originally identified because mutations in the ATRX gene cause a severe form of syndromal X-linked mental retardation associated with alpha-thalassemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP618352.RAXHZmqV7eBEgPklTl14-ixuRYt-h-Tw1_kPhT5K5fQWI130_provenance.
- NP618352.RAXHZmqV7eBEgPklTl14-ixuRYt-h-Tw1_kPhT5K5fQWI130_assertion evidence source_evidence_literature NP618352.RAXHZmqV7eBEgPklTl14-ixuRYt-h-Tw1_kPhT5K5fQWI130_provenance.
- NP618352.RAXHZmqV7eBEgPklTl14-ixuRYt-h-Tw1_kPhT5K5fQWI130_assertion SIO_000772 17609377 NP618352.RAXHZmqV7eBEgPklTl14-ixuRYt-h-Tw1_kPhT5K5fQWI130_provenance.
- NP618352.RAXHZmqV7eBEgPklTl14-ixuRYt-h-Tw1_kPhT5K5fQWI130_assertion wasDerivedFrom befree-2016 NP618352.RAXHZmqV7eBEgPklTl14-ixuRYt-h-Tw1_kPhT5K5fQWI130_provenance.
- NP618352.RAXHZmqV7eBEgPklTl14-ixuRYt-h-Tw1_kPhT5K5fQWI130_assertion wasGeneratedBy ECO_0000203 NP618352.RAXHZmqV7eBEgPklTl14-ixuRYt-h-Tw1_kPhT5K5fQWI130_provenance.