Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP684840.RA4i5tjAF3zc6gPf01s3MwHZiRQr1BQtpUBMZDbCYwEAs130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP684840.RA4i5tjAF3zc6gPf01s3MwHZiRQr1BQtpUBMZDbCYwEAs130_assertion type Assertion NP684840.RA4i5tjAF3zc6gPf01s3MwHZiRQr1BQtpUBMZDbCYwEAs130_head.
- NP684840.RA4i5tjAF3zc6gPf01s3MwHZiRQr1BQtpUBMZDbCYwEAs130_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." NP684840.RA4i5tjAF3zc6gPf01s3MwHZiRQr1BQtpUBMZDbCYwEAs130_provenance.
- NP684840.RA4i5tjAF3zc6gPf01s3MwHZiRQr1BQtpUBMZDbCYwEAs130_assertion evidence source_evidence_literature NP684840.RA4i5tjAF3zc6gPf01s3MwHZiRQr1BQtpUBMZDbCYwEAs130_provenance.
- NP684840.RA4i5tjAF3zc6gPf01s3MwHZiRQr1BQtpUBMZDbCYwEAs130_assertion SIO_000772 18663734 NP684840.RA4i5tjAF3zc6gPf01s3MwHZiRQr1BQtpUBMZDbCYwEAs130_provenance.
- NP684840.RA4i5tjAF3zc6gPf01s3MwHZiRQr1BQtpUBMZDbCYwEAs130_assertion wasDerivedFrom befree-2016 NP684840.RA4i5tjAF3zc6gPf01s3MwHZiRQr1BQtpUBMZDbCYwEAs130_provenance.
- NP684840.RA4i5tjAF3zc6gPf01s3MwHZiRQr1BQtpUBMZDbCYwEAs130_assertion wasGeneratedBy ECO_0000203 NP684840.RA4i5tjAF3zc6gPf01s3MwHZiRQr1BQtpUBMZDbCYwEAs130_provenance.