Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1186890.RA5gk2RTsZuV7KgdZUxDhFd2nEo24SLD_mMFIYepTIxto130_assertion> ?p ?o ?g. }
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- NP1186890.RA5gk2RTsZuV7KgdZUxDhFd2nEo24SLD_mMFIYepTIxto130_assertion type Assertion NP1186890.RA5gk2RTsZuV7KgdZUxDhFd2nEo24SLD_mMFIYepTIxto130_head.
- NP1186890.RA5gk2RTsZuV7KgdZUxDhFd2nEo24SLD_mMFIYepTIxto130_assertion description "[We report a three-generation family presenting a hereditary recurrent neuropathy without pathological changes in either PMP22 or SEPT9 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1186890.RA5gk2RTsZuV7KgdZUxDhFd2nEo24SLD_mMFIYepTIxto130_provenance.
- NP1186890.RA5gk2RTsZuV7KgdZUxDhFd2nEo24SLD_mMFIYepTIxto130_assertion evidence source_evidence_literature NP1186890.RA5gk2RTsZuV7KgdZUxDhFd2nEo24SLD_mMFIYepTIxto130_provenance.
- NP1186890.RA5gk2RTsZuV7KgdZUxDhFd2nEo24SLD_mMFIYepTIxto130_assertion SIO_000772 24878226 NP1186890.RA5gk2RTsZuV7KgdZUxDhFd2nEo24SLD_mMFIYepTIxto130_provenance.
- NP1186890.RA5gk2RTsZuV7KgdZUxDhFd2nEo24SLD_mMFIYepTIxto130_assertion wasDerivedFrom befree-2016 NP1186890.RA5gk2RTsZuV7KgdZUxDhFd2nEo24SLD_mMFIYepTIxto130_provenance.
- NP1186890.RA5gk2RTsZuV7KgdZUxDhFd2nEo24SLD_mMFIYepTIxto130_assertion wasGeneratedBy ECO_0000203 NP1186890.RA5gk2RTsZuV7KgdZUxDhFd2nEo24SLD_mMFIYepTIxto130_provenance.