Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP329151.RA5q9OOwyUOr2hwSWoaJVXea9eppt2OvH8a-_9ZQM61KQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP329151.RA5q9OOwyUOr2hwSWoaJVXea9eppt2OvH8a-_9ZQM61KQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP329151.RA5q9OOwyUOr2hwSWoaJVXea9eppt2OvH8a-_9ZQM61KQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP329151.RA5q9OOwyUOr2hwSWoaJVXea9eppt2OvH8a-_9ZQM61KQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP329151.RA5q9OOwyUOr2hwSWoaJVXea9eppt2OvH8a-_9ZQM61KQ130_provenance.
- NP329151.RA5q9OOwyUOr2hwSWoaJVXea9eppt2OvH8a-_9ZQM61KQ130_assertion wasGeneratedBy ECO_0000203 NP329151.RA5q9OOwyUOr2hwSWoaJVXea9eppt2OvH8a-_9ZQM61KQ130_provenance.
- NP329151.RA5q9OOwyUOr2hwSWoaJVXea9eppt2OvH8a-_9ZQM61KQ130_assertion wasDerivedFrom befree-2016 NP329151.RA5q9OOwyUOr2hwSWoaJVXea9eppt2OvH8a-_9ZQM61KQ130_provenance.
- NP329151.RA5q9OOwyUOr2hwSWoaJVXea9eppt2OvH8a-_9ZQM61KQ130_assertion SIO_000772 11535114 NP329151.RA5q9OOwyUOr2hwSWoaJVXea9eppt2OvH8a-_9ZQM61KQ130_provenance.
- NP329151.RA5q9OOwyUOr2hwSWoaJVXea9eppt2OvH8a-_9ZQM61KQ130_assertion evidence source_evidence_literature NP329151.RA5q9OOwyUOr2hwSWoaJVXea9eppt2OvH8a-_9ZQM61KQ130_provenance.
- NP329151.RA5q9OOwyUOr2hwSWoaJVXea9eppt2OvH8a-_9ZQM61KQ130_assertion description "[Similarities are drawn with the peripheral neuropathies Charcot-Marie-Tooth disease Type 1 (CMT1A) and hereditary neuropathy with liability to pressure palsies (HNPP) that are also caused by dosage effects and mutations in a single myelin protein gene (peripheral myelin protein 22, PMP-22).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP329151.RA5q9OOwyUOr2hwSWoaJVXea9eppt2OvH8a-_9ZQM61KQ130_provenance.