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- source_evidence_literature type ECO_0000212 NP588172.RAJ01_CT2HcswlEKBSeExBgkdrdI7ypP8RNDaEyKcoZfg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP588172.RAJ01_CT2HcswlEKBSeExBgkdrdI7ypP8RNDaEyKcoZfg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP588172.RAJ01_CT2HcswlEKBSeExBgkdrdI7ypP8RNDaEyKcoZfg130_provenance.
- NP588172.RAJ01_CT2HcswlEKBSeExBgkdrdI7ypP8RNDaEyKcoZfg130_assertion description "[Mutations in the mitochondrial fusion protein mitofusin 2 (MFN2) are the most commonly identified cause of Charcot-Marie-Tooth type 2 (CMT2), a dominantly inherited disease characterized by degeneration of peripheral sensory and motor axons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP588172.RAJ01_CT2HcswlEKBSeExBgkdrdI7ypP8RNDaEyKcoZfg130_provenance.
- NP588172.RAJ01_CT2HcswlEKBSeExBgkdrdI7ypP8RNDaEyKcoZfg130_assertion evidence source_evidence_literature NP588172.RAJ01_CT2HcswlEKBSeExBgkdrdI7ypP8RNDaEyKcoZfg130_provenance.
- NP588172.RAJ01_CT2HcswlEKBSeExBgkdrdI7ypP8RNDaEyKcoZfg130_assertion SIO_000772 17215403 NP588172.RAJ01_CT2HcswlEKBSeExBgkdrdI7ypP8RNDaEyKcoZfg130_provenance.
- NP588172.RAJ01_CT2HcswlEKBSeExBgkdrdI7ypP8RNDaEyKcoZfg130_assertion wasDerivedFrom befree-2016 NP588172.RAJ01_CT2HcswlEKBSeExBgkdrdI7ypP8RNDaEyKcoZfg130_provenance.
- NP588172.RAJ01_CT2HcswlEKBSeExBgkdrdI7ypP8RNDaEyKcoZfg130_assertion wasGeneratedBy ECO_0000203 NP588172.RAJ01_CT2HcswlEKBSeExBgkdrdI7ypP8RNDaEyKcoZfg130_provenance.
- befree-2016 importedOn "2016-02-19" NP588172.RAJ01_CT2HcswlEKBSeExBgkdrdI7ypP8RNDaEyKcoZfg130_provenance.