Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP477943.RAbCQgz-VD01C_OMeDK69FYxiGJalFLqT8LOLNkS3zbIw130_assertion> ?p ?o ?g. }
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- NP477943.RAbCQgz-VD01C_OMeDK69FYxiGJalFLqT8LOLNkS3zbIw130_assertion type Assertion NP477943.RAbCQgz-VD01C_OMeDK69FYxiGJalFLqT8LOLNkS3zbIw130_head.
- NP477943.RAbCQgz-VD01C_OMeDK69FYxiGJalFLqT8LOLNkS3zbIw130_assertion description "[These have recently included those that encode skeletal muscle alpha-actin in autosomal dominant and autosomal recessive nemaline myopathy, nebulin and slow alpha-tropomyosin in autosomal recessive nemaline myopathy, and desmin and alpha B-crystallin in desminopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP477943.RAbCQgz-VD01C_OMeDK69FYxiGJalFLqT8LOLNkS3zbIw130_provenance.
- NP477943.RAbCQgz-VD01C_OMeDK69FYxiGJalFLqT8LOLNkS3zbIw130_assertion evidence source_evidence_literature NP477943.RAbCQgz-VD01C_OMeDK69FYxiGJalFLqT8LOLNkS3zbIw130_provenance.
- NP477943.RAbCQgz-VD01C_OMeDK69FYxiGJalFLqT8LOLNkS3zbIw130_assertion SIO_000772 10590887 NP477943.RAbCQgz-VD01C_OMeDK69FYxiGJalFLqT8LOLNkS3zbIw130_provenance.
- NP477943.RAbCQgz-VD01C_OMeDK69FYxiGJalFLqT8LOLNkS3zbIw130_assertion wasDerivedFrom befree-20140225 NP477943.RAbCQgz-VD01C_OMeDK69FYxiGJalFLqT8LOLNkS3zbIw130_provenance.
- NP477943.RAbCQgz-VD01C_OMeDK69FYxiGJalFLqT8LOLNkS3zbIw130_assertion wasGeneratedBy ECO_0000203 NP477943.RAbCQgz-VD01C_OMeDK69FYxiGJalFLqT8LOLNkS3zbIw130_provenance.