Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP632468.RAgMPdN8t_m1tvy5ueIwEG8k6SDYWYiwDL14EdIvmmbaM130_assertion> ?p ?o ?g. }
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- NP632468.RAgMPdN8t_m1tvy5ueIwEG8k6SDYWYiwDL14EdIvmmbaM130_assertion type Assertion NP632468.RAgMPdN8t_m1tvy5ueIwEG8k6SDYWYiwDL14EdIvmmbaM130_head.
- NP632468.RAgMPdN8t_m1tvy5ueIwEG8k6SDYWYiwDL14EdIvmmbaM130_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." NP632468.RAgMPdN8t_m1tvy5ueIwEG8k6SDYWYiwDL14EdIvmmbaM130_provenance.
- NP632468.RAgMPdN8t_m1tvy5ueIwEG8k6SDYWYiwDL14EdIvmmbaM130_assertion evidence source_evidence_literature NP632468.RAgMPdN8t_m1tvy5ueIwEG8k6SDYWYiwDL14EdIvmmbaM130_provenance.
- NP632468.RAgMPdN8t_m1tvy5ueIwEG8k6SDYWYiwDL14EdIvmmbaM130_assertion SIO_000772 18663734 NP632468.RAgMPdN8t_m1tvy5ueIwEG8k6SDYWYiwDL14EdIvmmbaM130_provenance.
- NP632468.RAgMPdN8t_m1tvy5ueIwEG8k6SDYWYiwDL14EdIvmmbaM130_assertion wasDerivedFrom befree-20150227 NP632468.RAgMPdN8t_m1tvy5ueIwEG8k6SDYWYiwDL14EdIvmmbaM130_provenance.
- NP632468.RAgMPdN8t_m1tvy5ueIwEG8k6SDYWYiwDL14EdIvmmbaM130_assertion wasGeneratedBy ECO_0000203 NP632468.RAgMPdN8t_m1tvy5ueIwEG8k6SDYWYiwDL14EdIvmmbaM130_provenance.