Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP433512.RALrwXYqRbHYwb3jjV6jzCGgW04NxJqkRo_yjSpwj0TCY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP433512.RALrwXYqRbHYwb3jjV6jzCGgW04NxJqkRo_yjSpwj0TCY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP433512.RALrwXYqRbHYwb3jjV6jzCGgW04NxJqkRo_yjSpwj0TCY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP433512.RALrwXYqRbHYwb3jjV6jzCGgW04NxJqkRo_yjSpwj0TCY130_provenance.
- NP433512.RALrwXYqRbHYwb3jjV6jzCGgW04NxJqkRo_yjSpwj0TCY130_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." NP433512.RALrwXYqRbHYwb3jjV6jzCGgW04NxJqkRo_yjSpwj0TCY130_provenance.
- NP433512.RALrwXYqRbHYwb3jjV6jzCGgW04NxJqkRo_yjSpwj0TCY130_assertion evidence source_evidence_literature NP433512.RALrwXYqRbHYwb3jjV6jzCGgW04NxJqkRo_yjSpwj0TCY130_provenance.
- NP433512.RALrwXYqRbHYwb3jjV6jzCGgW04NxJqkRo_yjSpwj0TCY130_assertion SIO_000772 14991352 NP433512.RALrwXYqRbHYwb3jjV6jzCGgW04NxJqkRo_yjSpwj0TCY130_provenance.
- NP433512.RALrwXYqRbHYwb3jjV6jzCGgW04NxJqkRo_yjSpwj0TCY130_assertion wasDerivedFrom befree-2016 NP433512.RALrwXYqRbHYwb3jjV6jzCGgW04NxJqkRo_yjSpwj0TCY130_provenance.
- NP433512.RALrwXYqRbHYwb3jjV6jzCGgW04NxJqkRo_yjSpwj0TCY130_assertion wasGeneratedBy ECO_0000203 NP433512.RALrwXYqRbHYwb3jjV6jzCGgW04NxJqkRo_yjSpwj0TCY130_provenance.
- befree-2016 importedOn "2016-02-19" NP433512.RALrwXYqRbHYwb3jjV6jzCGgW04NxJqkRo_yjSpwj0TCY130_provenance.