Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1323774.RAABAV911kA4C17gycwAFLa34iBJSy6TisyX89kwHBjAQ130_assertion> ?p ?o ?g. }
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- NP1323774.RAABAV911kA4C17gycwAFLa34iBJSy6TisyX89kwHBjAQ130_assertion type Assertion NP1323774.RAABAV911kA4C17gycwAFLa34iBJSy6TisyX89kwHBjAQ130_head.
- NP1323774.RAABAV911kA4C17gycwAFLa34iBJSy6TisyX89kwHBjAQ130_assertion description "[Dejerine-Sottas disease, also called hereditary motor and sensory neuropathy type III (HMSNIII), is a severe, infantile onset demyelinating polyneuropathy syndrome that may be associated with point mutations in either the PMP22 gene of the P0 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1323774.RAABAV911kA4C17gycwAFLa34iBJSy6TisyX89kwHBjAQ130_provenance.
- NP1323774.RAABAV911kA4C17gycwAFLa34iBJSy6TisyX89kwHBjAQ130_assertion evidence source_evidence_literature NP1323774.RAABAV911kA4C17gycwAFLa34iBJSy6TisyX89kwHBjAQ130_provenance.
- NP1323774.RAABAV911kA4C17gycwAFLa34iBJSy6TisyX89kwHBjAQ130_assertion SIO_000772 7849745 NP1323774.RAABAV911kA4C17gycwAFLa34iBJSy6TisyX89kwHBjAQ130_provenance.
- NP1323774.RAABAV911kA4C17gycwAFLa34iBJSy6TisyX89kwHBjAQ130_assertion wasDerivedFrom befree-2016 NP1323774.RAABAV911kA4C17gycwAFLa34iBJSy6TisyX89kwHBjAQ130_provenance.
- NP1323774.RAABAV911kA4C17gycwAFLa34iBJSy6TisyX89kwHBjAQ130_assertion wasGeneratedBy ECO_0000203 NP1323774.RAABAV911kA4C17gycwAFLa34iBJSy6TisyX89kwHBjAQ130_provenance.