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- source_evidence_literature type ECO_0000212 NP684837.RAtABTDGGIFpmkGRxzB3TsyV7MNW-r545zO91ymQUJRlI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP684837.RAtABTDGGIFpmkGRxzB3TsyV7MNW-r545zO91ymQUJRlI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP684837.RAtABTDGGIFpmkGRxzB3TsyV7MNW-r545zO91ymQUJRlI130_provenance.
- NP684837.RAtABTDGGIFpmkGRxzB3TsyV7MNW-r545zO91ymQUJRlI130_assertion description "[Therefore, such MPZ gene mutations should be searched for in cases of demyelinating neuropathy with acute nerve compression as well as in cases of the HNPP phenotype associated with normal the PMP22 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP684837.RAtABTDGGIFpmkGRxzB3TsyV7MNW-r545zO91ymQUJRlI130_provenance.
- NP684837.RAtABTDGGIFpmkGRxzB3TsyV7MNW-r545zO91ymQUJRlI130_assertion evidence source_evidence_literature NP684837.RAtABTDGGIFpmkGRxzB3TsyV7MNW-r545zO91ymQUJRlI130_provenance.
- NP684837.RAtABTDGGIFpmkGRxzB3TsyV7MNW-r545zO91ymQUJRlI130_assertion SIO_000772 18663734 NP684837.RAtABTDGGIFpmkGRxzB3TsyV7MNW-r545zO91ymQUJRlI130_provenance.
- NP684837.RAtABTDGGIFpmkGRxzB3TsyV7MNW-r545zO91ymQUJRlI130_assertion wasDerivedFrom befree-2016 NP684837.RAtABTDGGIFpmkGRxzB3TsyV7MNW-r545zO91ymQUJRlI130_provenance.
- NP684837.RAtABTDGGIFpmkGRxzB3TsyV7MNW-r545zO91ymQUJRlI130_assertion wasGeneratedBy ECO_0000203 NP684837.RAtABTDGGIFpmkGRxzB3TsyV7MNW-r545zO91ymQUJRlI130_provenance.
- befree-2016 importedOn "2016-02-19" NP684837.RAtABTDGGIFpmkGRxzB3TsyV7MNW-r545zO91ymQUJRlI130_provenance.