Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP588171.RAaC6l3R50U2ZNAs0Pn6T3zK03WQ6pe-HCqfLPmn00Ge8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP588171.RAaC6l3R50U2ZNAs0Pn6T3zK03WQ6pe-HCqfLPmn00Ge8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP588171.RAaC6l3R50U2ZNAs0Pn6T3zK03WQ6pe-HCqfLPmn00Ge8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP588171.RAaC6l3R50U2ZNAs0Pn6T3zK03WQ6pe-HCqfLPmn00Ge8130_provenance.
- NP588171.RAaC6l3R50U2ZNAs0Pn6T3zK03WQ6pe-HCqfLPmn00Ge8130_assertion description "[To explore how MFN2 mutations lead to degeneration of peripheral axons, we expressed neuropathy-associated forms of MFN2 in cultured dorsal root ganglion neurons, cells preferentially affected in CMT2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP588171.RAaC6l3R50U2ZNAs0Pn6T3zK03WQ6pe-HCqfLPmn00Ge8130_provenance.
- NP588171.RAaC6l3R50U2ZNAs0Pn6T3zK03WQ6pe-HCqfLPmn00Ge8130_assertion evidence source_evidence_literature NP588171.RAaC6l3R50U2ZNAs0Pn6T3zK03WQ6pe-HCqfLPmn00Ge8130_provenance.
- NP588171.RAaC6l3R50U2ZNAs0Pn6T3zK03WQ6pe-HCqfLPmn00Ge8130_assertion SIO_000772 17215403 NP588171.RAaC6l3R50U2ZNAs0Pn6T3zK03WQ6pe-HCqfLPmn00Ge8130_provenance.
- NP588171.RAaC6l3R50U2ZNAs0Pn6T3zK03WQ6pe-HCqfLPmn00Ge8130_assertion wasDerivedFrom befree-2016 NP588171.RAaC6l3R50U2ZNAs0Pn6T3zK03WQ6pe-HCqfLPmn00Ge8130_provenance.
- NP588171.RAaC6l3R50U2ZNAs0Pn6T3zK03WQ6pe-HCqfLPmn00Ge8130_assertion wasGeneratedBy ECO_0000203 NP588171.RAaC6l3R50U2ZNAs0Pn6T3zK03WQ6pe-HCqfLPmn00Ge8130_provenance.
- befree-2016 importedOn "2016-02-19" NP588171.RAaC6l3R50U2ZNAs0Pn6T3zK03WQ6pe-HCqfLPmn00Ge8130_provenance.