Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP924908.RAdzQQgX4C1J2qtU3-g0kR1hzRzRvzGNFIkbPFaKjyDnI130_assertion> ?p ?o ?g. }
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- NP924908.RAdzQQgX4C1J2qtU3-g0kR1hzRzRvzGNFIkbPFaKjyDnI130_assertion type Assertion NP924908.RAdzQQgX4C1J2qtU3-g0kR1hzRzRvzGNFIkbPFaKjyDnI130_head.
- NP924908.RAdzQQgX4C1J2qtU3-g0kR1hzRzRvzGNFIkbPFaKjyDnI130_assertion description "[Dystrophin expression and genotypic analysis of two cases of benign X linked myopathy (McLeod's syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP924908.RAdzQQgX4C1J2qtU3-g0kR1hzRzRvzGNFIkbPFaKjyDnI130_provenance.
- NP924908.RAdzQQgX4C1J2qtU3-g0kR1hzRzRvzGNFIkbPFaKjyDnI130_assertion evidence source_evidence_literature NP924908.RAdzQQgX4C1J2qtU3-g0kR1hzRzRvzGNFIkbPFaKjyDnI130_provenance.
- NP924908.RAdzQQgX4C1J2qtU3-g0kR1hzRzRvzGNFIkbPFaKjyDnI130_assertion SIO_000772 2193159 NP924908.RAdzQQgX4C1J2qtU3-g0kR1hzRzRvzGNFIkbPFaKjyDnI130_provenance.
- NP924908.RAdzQQgX4C1J2qtU3-g0kR1hzRzRvzGNFIkbPFaKjyDnI130_assertion wasDerivedFrom befree-2016 NP924908.RAdzQQgX4C1J2qtU3-g0kR1hzRzRvzGNFIkbPFaKjyDnI130_provenance.
- NP924908.RAdzQQgX4C1J2qtU3-g0kR1hzRzRvzGNFIkbPFaKjyDnI130_assertion wasGeneratedBy ECO_0000203 NP924908.RAdzQQgX4C1J2qtU3-g0kR1hzRzRvzGNFIkbPFaKjyDnI130_provenance.