Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP985021.RAP3rURTZMKE7tksq9JPpN6tvBCdrxHBqiFFYVvo_3-as130_assertion> ?p ?o ?g. }
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- NP985021.RAP3rURTZMKE7tksq9JPpN6tvBCdrxHBqiFFYVvo_3-as130_assertion type Assertion NP985021.RAP3rURTZMKE7tksq9JPpN6tvBCdrxHBqiFFYVvo_3-as130_head.
- NP985021.RAP3rURTZMKE7tksq9JPpN6tvBCdrxHBqiFFYVvo_3-as130_assertion description "[Notably, H3K9me3-pocket mutants and ATR-X syndrome mutants are defective in both H3K9me3 binding and localization at pericentromeric heterochromatin; thus, we have discovered a unique histone-recognition mechanism underlying the ATR-X etiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP985021.RAP3rURTZMKE7tksq9JPpN6tvBCdrxHBqiFFYVvo_3-as130_provenance.
- NP985021.RAP3rURTZMKE7tksq9JPpN6tvBCdrxHBqiFFYVvo_3-as130_assertion evidence source_evidence_literature NP985021.RAP3rURTZMKE7tksq9JPpN6tvBCdrxHBqiFFYVvo_3-as130_provenance.
- NP985021.RAP3rURTZMKE7tksq9JPpN6tvBCdrxHBqiFFYVvo_3-as130_assertion SIO_000772 21666679 NP985021.RAP3rURTZMKE7tksq9JPpN6tvBCdrxHBqiFFYVvo_3-as130_provenance.
- NP985021.RAP3rURTZMKE7tksq9JPpN6tvBCdrxHBqiFFYVvo_3-as130_assertion wasDerivedFrom befree-20150227 NP985021.RAP3rURTZMKE7tksq9JPpN6tvBCdrxHBqiFFYVvo_3-as130_provenance.
- NP985021.RAP3rURTZMKE7tksq9JPpN6tvBCdrxHBqiFFYVvo_3-as130_assertion wasGeneratedBy ECO_0000203 NP985021.RAP3rURTZMKE7tksq9JPpN6tvBCdrxHBqiFFYVvo_3-as130_provenance.