Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP583190.RA--8X_N7IGaXF7VxgbfoPswT6kzIvkiDeVNmDt0Zy65o130_assertion> ?p ?o ?g. }
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- NP583190.RA--8X_N7IGaXF7VxgbfoPswT6kzIvkiDeVNmDt0Zy65o130_assertion type Assertion NP583190.RA--8X_N7IGaXF7VxgbfoPswT6kzIvkiDeVNmDt0Zy65o130_head.
- NP583190.RA--8X_N7IGaXF7VxgbfoPswT6kzIvkiDeVNmDt0Zy65o130_assertion description "[We recently described a new autosomal dominant myopathy (OMIM #605637) associated with a missense mutation in the myosin heavy chain (MyHC) IIa gene ( MYH2), which encodes for the fast myosin isoform that is expressed in type 2A muscle fibers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583190.RA--8X_N7IGaXF7VxgbfoPswT6kzIvkiDeVNmDt0Zy65o130_provenance.
- NP583190.RA--8X_N7IGaXF7VxgbfoPswT6kzIvkiDeVNmDt0Zy65o130_assertion evidence source_evidence_literature NP583190.RA--8X_N7IGaXF7VxgbfoPswT6kzIvkiDeVNmDt0Zy65o130_provenance.
- NP583190.RA--8X_N7IGaXF7VxgbfoPswT6kzIvkiDeVNmDt0Zy65o130_assertion SIO_000772 14991352 NP583190.RA--8X_N7IGaXF7VxgbfoPswT6kzIvkiDeVNmDt0Zy65o130_provenance.
- NP583190.RA--8X_N7IGaXF7VxgbfoPswT6kzIvkiDeVNmDt0Zy65o130_assertion wasDerivedFrom befree-20150227 NP583190.RA--8X_N7IGaXF7VxgbfoPswT6kzIvkiDeVNmDt0Zy65o130_provenance.
- NP583190.RA--8X_N7IGaXF7VxgbfoPswT6kzIvkiDeVNmDt0Zy65o130_assertion wasGeneratedBy ECO_0000203 NP583190.RA--8X_N7IGaXF7VxgbfoPswT6kzIvkiDeVNmDt0Zy65o130_provenance.