Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP4198.RARxk-Gb93YuugosFEJcCpS_BeYrOWp-_wZMvn5GCQKqo130_assertion> ?p ?o ?g. }
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- NP4198.RARxk-Gb93YuugosFEJcCpS_BeYrOWp-_wZMvn5GCQKqo130_assertion type Assertion NP4198.RARxk-Gb93YuugosFEJcCpS_BeYrOWp-_wZMvn5GCQKqo130_head.
- NP4198.RARxk-Gb93YuugosFEJcCpS_BeYrOWp-_wZMvn5GCQKqo130_assertion wasGeneratedBy ECO_0000218 NP4198.RARxk-Gb93YuugosFEJcCpS_BeYrOWp-_wZMvn5GCQKqo130_provenance.
- NP4198.RARxk-Gb93YuugosFEJcCpS_BeYrOWp-_wZMvn5GCQKqo130_assertion wasDerivedFrom uniprot-20130724 NP4198.RARxk-Gb93YuugosFEJcCpS_BeYrOWp-_wZMvn5GCQKqo130_provenance.
- NP4198.RARxk-Gb93YuugosFEJcCpS_BeYrOWp-_wZMvn5GCQKqo130_assertion SIO_000772 17005396 NP4198.RARxk-Gb93YuugosFEJcCpS_BeYrOWp-_wZMvn5GCQKqo130_provenance.
- NP4198.RARxk-Gb93YuugosFEJcCpS_BeYrOWp-_wZMvn5GCQKqo130_assertion evidence source_evidence_curated NP4198.RARxk-Gb93YuugosFEJcCpS_BeYrOWp-_wZMvn5GCQKqo130_provenance.
- NP4198.RARxk-Gb93YuugosFEJcCpS_BeYrOWp-_wZMvn5GCQKqo130_assertion description "[Extreme phenotypic variability in a German family with X-linked myotubular myopathy associated with E404K mutation in MTM1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4198.RARxk-Gb93YuugosFEJcCpS_BeYrOWp-_wZMvn5GCQKqo130_provenance.