Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP469876.RA0Co32g3st7vLmeltT-EhR0zNGddoARPxnyczSrNisOE130_assertion> ?p ?o ?g. }
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- NP469876.RA0Co32g3st7vLmeltT-EhR0zNGddoARPxnyczSrNisOE130_assertion type Assertion NP469876.RA0Co32g3st7vLmeltT-EhR0zNGddoARPxnyczSrNisOE130_head.
- NP469876.RA0Co32g3st7vLmeltT-EhR0zNGddoARPxnyczSrNisOE130_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." NP469876.RA0Co32g3st7vLmeltT-EhR0zNGddoARPxnyczSrNisOE130_provenance.
- NP469876.RA0Co32g3st7vLmeltT-EhR0zNGddoARPxnyczSrNisOE130_assertion evidence source_evidence_literature NP469876.RA0Co32g3st7vLmeltT-EhR0zNGddoARPxnyczSrNisOE130_provenance.
- NP469876.RA0Co32g3st7vLmeltT-EhR0zNGddoARPxnyczSrNisOE130_assertion SIO_000772 18663734 NP469876.RA0Co32g3st7vLmeltT-EhR0zNGddoARPxnyczSrNisOE130_provenance.
- NP469876.RA0Co32g3st7vLmeltT-EhR0zNGddoARPxnyczSrNisOE130_assertion wasDerivedFrom befree-20140225 NP469876.RA0Co32g3st7vLmeltT-EhR0zNGddoARPxnyczSrNisOE130_provenance.
- NP469876.RA0Co32g3st7vLmeltT-EhR0zNGddoARPxnyczSrNisOE130_assertion wasGeneratedBy ECO_0000203 NP469876.RA0Co32g3st7vLmeltT-EhR0zNGddoARPxnyczSrNisOE130_provenance.