Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1398193.RAq2pm1q-Kl_URwaVhjdou7vib4I40H03wBGuVXt1rTyI130_assertion> ?p ?o ?g. }
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- NP1398193.RAq2pm1q-Kl_URwaVhjdou7vib4I40H03wBGuVXt1rTyI130_assertion type Assertion NP1398193.RAq2pm1q-Kl_URwaVhjdou7vib4I40H03wBGuVXt1rTyI130_head.
- NP1398193.RAq2pm1q-Kl_URwaVhjdou7vib4I40H03wBGuVXt1rTyI130_assertion description "[p94 (calpain3), a muscle-specific member of the calpain family, has been shown to be responsible for limb-girdle muscular dystrophy type 2A (LGMD2A), a form of autosomal recessive and progressive neuromuscular disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1398193.RAq2pm1q-Kl_URwaVhjdou7vib4I40H03wBGuVXt1rTyI130_provenance.
- NP1398193.RAq2pm1q-Kl_URwaVhjdou7vib4I40H03wBGuVXt1rTyI130_assertion evidence source_evidence_literature NP1398193.RAq2pm1q-Kl_URwaVhjdou7vib4I40H03wBGuVXt1rTyI130_provenance.
- NP1398193.RAq2pm1q-Kl_URwaVhjdou7vib4I40H03wBGuVXt1rTyI130_assertion SIO_000772 9642272 NP1398193.RAq2pm1q-Kl_URwaVhjdou7vib4I40H03wBGuVXt1rTyI130_provenance.
- NP1398193.RAq2pm1q-Kl_URwaVhjdou7vib4I40H03wBGuVXt1rTyI130_assertion wasDerivedFrom befree-2016 NP1398193.RAq2pm1q-Kl_URwaVhjdou7vib4I40H03wBGuVXt1rTyI130_provenance.
- NP1398193.RAq2pm1q-Kl_URwaVhjdou7vib4I40H03wBGuVXt1rTyI130_assertion wasGeneratedBy ECO_0000203 NP1398193.RAq2pm1q-Kl_URwaVhjdou7vib4I40H03wBGuVXt1rTyI130_provenance.