Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP555807.RAFl4dDiweL3mQg9GjKP_dnZgoQ0KS_K7ofT_mIRCRKPQ130_assertion> ?p ?o ?g. }
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- NP555807.RAFl4dDiweL3mQg9GjKP_dnZgoQ0KS_K7ofT_mIRCRKPQ130_assertion type Assertion NP555807.RAFl4dDiweL3mQg9GjKP_dnZgoQ0KS_K7ofT_mIRCRKPQ130_head.
- NP555807.RAFl4dDiweL3mQg9GjKP_dnZgoQ0KS_K7ofT_mIRCRKPQ130_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." NP555807.RAFl4dDiweL3mQg9GjKP_dnZgoQ0KS_K7ofT_mIRCRKPQ130_provenance.
- NP555807.RAFl4dDiweL3mQg9GjKP_dnZgoQ0KS_K7ofT_mIRCRKPQ130_assertion evidence source_evidence_literature NP555807.RAFl4dDiweL3mQg9GjKP_dnZgoQ0KS_K7ofT_mIRCRKPQ130_provenance.
- NP555807.RAFl4dDiweL3mQg9GjKP_dnZgoQ0KS_K7ofT_mIRCRKPQ130_assertion SIO_000772 18663734 NP555807.RAFl4dDiweL3mQg9GjKP_dnZgoQ0KS_K7ofT_mIRCRKPQ130_provenance.
- NP555807.RAFl4dDiweL3mQg9GjKP_dnZgoQ0KS_K7ofT_mIRCRKPQ130_assertion wasDerivedFrom befree-20140225 NP555807.RAFl4dDiweL3mQg9GjKP_dnZgoQ0KS_K7ofT_mIRCRKPQ130_provenance.
- NP555807.RAFl4dDiweL3mQg9GjKP_dnZgoQ0KS_K7ofT_mIRCRKPQ130_assertion wasGeneratedBy ECO_0000203 NP555807.RAFl4dDiweL3mQg9GjKP_dnZgoQ0KS_K7ofT_mIRCRKPQ130_provenance.