Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP317020.RA-7rpeBvfpUAi_bLdq8-WuMh-kN4IDmxWpASj2VR4IIo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP317020.RA-7rpeBvfpUAi_bLdq8-WuMh-kN4IDmxWpASj2VR4IIo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP317020.RA-7rpeBvfpUAi_bLdq8-WuMh-kN4IDmxWpASj2VR4IIo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP317020.RA-7rpeBvfpUAi_bLdq8-WuMh-kN4IDmxWpASj2VR4IIo130_provenance.
- NP317020.RA-7rpeBvfpUAi_bLdq8-WuMh-kN4IDmxWpASj2VR4IIo130_assertion description "[Calpain 3 is the muscle-specific member of the calcium activated neutral protease family and primary mutations in the CAPN3 gene cause limb girdle muscular dystrophy type 2A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP317020.RA-7rpeBvfpUAi_bLdq8-WuMh-kN4IDmxWpASj2VR4IIo130_provenance.
- NP317020.RA-7rpeBvfpUAi_bLdq8-WuMh-kN4IDmxWpASj2VR4IIo130_assertion evidence source_evidence_literature NP317020.RA-7rpeBvfpUAi_bLdq8-WuMh-kN4IDmxWpASj2VR4IIo130_provenance.
- NP317020.RA-7rpeBvfpUAi_bLdq8-WuMh-kN4IDmxWpASj2VR4IIo130_assertion SIO_000772 11053681 NP317020.RA-7rpeBvfpUAi_bLdq8-WuMh-kN4IDmxWpASj2VR4IIo130_provenance.
- NP317020.RA-7rpeBvfpUAi_bLdq8-WuMh-kN4IDmxWpASj2VR4IIo130_assertion wasDerivedFrom befree-20140225 NP317020.RA-7rpeBvfpUAi_bLdq8-WuMh-kN4IDmxWpASj2VR4IIo130_provenance.
- NP317020.RA-7rpeBvfpUAi_bLdq8-WuMh-kN4IDmxWpASj2VR4IIo130_assertion wasGeneratedBy ECO_0000203 NP317020.RA-7rpeBvfpUAi_bLdq8-WuMh-kN4IDmxWpASj2VR4IIo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP317020.RA-7rpeBvfpUAi_bLdq8-WuMh-kN4IDmxWpASj2VR4IIo130_provenance.