Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1322377.RAVVOG9JBqcR-xgZAl1S6cO-k3AsJtQz4y6CPWK9jfHzo130_assertion> ?p ?o ?g. }
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- NP1322377.RAVVOG9JBqcR-xgZAl1S6cO-k3AsJtQz4y6CPWK9jfHzo130_assertion type Assertion NP1322377.RAVVOG9JBqcR-xgZAl1S6cO-k3AsJtQz4y6CPWK9jfHzo130_head.
- NP1322377.RAVVOG9JBqcR-xgZAl1S6cO-k3AsJtQz4y6CPWK9jfHzo130_assertion description "[Dejerine-Sottas disease is a severe, infantile-onset demyelinating polyneuropathy that may be associated with point mutations in either the PMP22 gene or the P0 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1322377.RAVVOG9JBqcR-xgZAl1S6cO-k3AsJtQz4y6CPWK9jfHzo130_provenance.
- NP1322377.RAVVOG9JBqcR-xgZAl1S6cO-k3AsJtQz4y6CPWK9jfHzo130_assertion evidence source_evidence_literature NP1322377.RAVVOG9JBqcR-xgZAl1S6cO-k3AsJtQz4y6CPWK9jfHzo130_provenance.
- NP1322377.RAVVOG9JBqcR-xgZAl1S6cO-k3AsJtQz4y6CPWK9jfHzo130_assertion SIO_000772 7804455 NP1322377.RAVVOG9JBqcR-xgZAl1S6cO-k3AsJtQz4y6CPWK9jfHzo130_provenance.
- NP1322377.RAVVOG9JBqcR-xgZAl1S6cO-k3AsJtQz4y6CPWK9jfHzo130_assertion wasDerivedFrom befree-2016 NP1322377.RAVVOG9JBqcR-xgZAl1S6cO-k3AsJtQz4y6CPWK9jfHzo130_provenance.
- NP1322377.RAVVOG9JBqcR-xgZAl1S6cO-k3AsJtQz4y6CPWK9jfHzo130_assertion wasGeneratedBy ECO_0000203 NP1322377.RAVVOG9JBqcR-xgZAl1S6cO-k3AsJtQz4y6CPWK9jfHzo130_provenance.