Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP352607.RAWkpWoRy-MPtGYka-U-b_dfw3R59NOBHzwKcNCY1xqTY130_assertion> ?p ?o ?g. }
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- NP352607.RAWkpWoRy-MPtGYka-U-b_dfw3R59NOBHzwKcNCY1xqTY130_assertion type Assertion NP352607.RAWkpWoRy-MPtGYka-U-b_dfw3R59NOBHzwKcNCY1xqTY130_head.
- NP352607.RAWkpWoRy-MPtGYka-U-b_dfw3R59NOBHzwKcNCY1xqTY130_assertion description "[Mutations of the human desmin gene on chromosome 2q35 cause a familial or sporadic form of skeletal myopathy frequently associated with cardiac abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP352607.RAWkpWoRy-MPtGYka-U-b_dfw3R59NOBHzwKcNCY1xqTY130_provenance.
- NP352607.RAWkpWoRy-MPtGYka-U-b_dfw3R59NOBHzwKcNCY1xqTY130_assertion evidence source_evidence_literature NP352607.RAWkpWoRy-MPtGYka-U-b_dfw3R59NOBHzwKcNCY1xqTY130_provenance.
- NP352607.RAWkpWoRy-MPtGYka-U-b_dfw3R59NOBHzwKcNCY1xqTY130_assertion SIO_000772 17635637 NP352607.RAWkpWoRy-MPtGYka-U-b_dfw3R59NOBHzwKcNCY1xqTY130_provenance.
- NP352607.RAWkpWoRy-MPtGYka-U-b_dfw3R59NOBHzwKcNCY1xqTY130_assertion wasDerivedFrom befree-20150227 NP352607.RAWkpWoRy-MPtGYka-U-b_dfw3R59NOBHzwKcNCY1xqTY130_provenance.
- NP352607.RAWkpWoRy-MPtGYka-U-b_dfw3R59NOBHzwKcNCY1xqTY130_assertion wasGeneratedBy ECO_0000203 NP352607.RAWkpWoRy-MPtGYka-U-b_dfw3R59NOBHzwKcNCY1xqTY130_provenance.