Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP832470.RAP8fCc_9VtWBPHDhoduglhV-j7knB9iaUMN1RLiBHwps130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP832470.RAP8fCc_9VtWBPHDhoduglhV-j7knB9iaUMN1RLiBHwps130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP832470.RAP8fCc_9VtWBPHDhoduglhV-j7knB9iaUMN1RLiBHwps130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP832470.RAP8fCc_9VtWBPHDhoduglhV-j7knB9iaUMN1RLiBHwps130_provenance.
- NP832470.RAP8fCc_9VtWBPHDhoduglhV-j7knB9iaUMN1RLiBHwps130_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." NP832470.RAP8fCc_9VtWBPHDhoduglhV-j7knB9iaUMN1RLiBHwps130_provenance.
- NP832470.RAP8fCc_9VtWBPHDhoduglhV-j7knB9iaUMN1RLiBHwps130_assertion evidence source_evidence_literature NP832470.RAP8fCc_9VtWBPHDhoduglhV-j7knB9iaUMN1RLiBHwps130_provenance.
- NP832470.RAP8fCc_9VtWBPHDhoduglhV-j7knB9iaUMN1RLiBHwps130_assertion SIO_000772 17215403 NP832470.RAP8fCc_9VtWBPHDhoduglhV-j7knB9iaUMN1RLiBHwps130_provenance.
- NP832470.RAP8fCc_9VtWBPHDhoduglhV-j7knB9iaUMN1RLiBHwps130_assertion wasDerivedFrom befree-20150227 NP832470.RAP8fCc_9VtWBPHDhoduglhV-j7knB9iaUMN1RLiBHwps130_provenance.
- NP832470.RAP8fCc_9VtWBPHDhoduglhV-j7knB9iaUMN1RLiBHwps130_assertion wasGeneratedBy ECO_0000203 NP832470.RAP8fCc_9VtWBPHDhoduglhV-j7knB9iaUMN1RLiBHwps130_provenance.
- befree-20150227 importedOn "2015-02-27" NP832470.RAP8fCc_9VtWBPHDhoduglhV-j7knB9iaUMN1RLiBHwps130_provenance.