Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP889717.RAXhB1vU2T6e7aAjqTArk74OAun5OmYfvFG-zywVWFGF8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP889717.RAXhB1vU2T6e7aAjqTArk74OAun5OmYfvFG-zywVWFGF8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP889717.RAXhB1vU2T6e7aAjqTArk74OAun5OmYfvFG-zywVWFGF8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP889717.RAXhB1vU2T6e7aAjqTArk74OAun5OmYfvFG-zywVWFGF8130_provenance.
- NP889717.RAXhB1vU2T6e7aAjqTArk74OAun5OmYfvFG-zywVWFGF8130_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." NP889717.RAXhB1vU2T6e7aAjqTArk74OAun5OmYfvFG-zywVWFGF8130_provenance.
- NP889717.RAXhB1vU2T6e7aAjqTArk74OAun5OmYfvFG-zywVWFGF8130_assertion evidence source_evidence_literature NP889717.RAXhB1vU2T6e7aAjqTArk74OAun5OmYfvFG-zywVWFGF8130_provenance.
- NP889717.RAXhB1vU2T6e7aAjqTArk74OAun5OmYfvFG-zywVWFGF8130_assertion SIO_000772 9642272 NP889717.RAXhB1vU2T6e7aAjqTArk74OAun5OmYfvFG-zywVWFGF8130_provenance.
- NP889717.RAXhB1vU2T6e7aAjqTArk74OAun5OmYfvFG-zywVWFGF8130_assertion wasDerivedFrom befree-20150227 NP889717.RAXhB1vU2T6e7aAjqTArk74OAun5OmYfvFG-zywVWFGF8130_provenance.
- NP889717.RAXhB1vU2T6e7aAjqTArk74OAun5OmYfvFG-zywVWFGF8130_assertion wasGeneratedBy ECO_0000203 NP889717.RAXhB1vU2T6e7aAjqTArk74OAun5OmYfvFG-zywVWFGF8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP889717.RAXhB1vU2T6e7aAjqTArk74OAun5OmYfvFG-zywVWFGF8130_provenance.